BETTER_PH-2002说明书

Standardize patient hygieneSageUrine management/bathing/incontinence care/meatal cleansingWhat are the challenges to providing the best care?Inconsistent applicationThe dosage and delivery process often varies greatly between nurses, units, and facilities.Multiple-step products require more time and aren’t always available orpart of the workflow. Potential spills and clean-up also add time to the process.Lack of aneffective alternativeFollowing guidelines and protocols regarding catheter use is difficult when patients need urinary management assistance.Standardize your patient hygiene programOur products can help you address the patient cleansing challenges of CAUTI & IAD. We provide innovative solutionsthat help standardize your patient hygiene protocol– efficiently, consistently, and safely.Patient hygiene products: committed to qualityOur patient hygiene products are designed, manufactured, and distributed from a state-of-the-art facility equipped with the latest quality control systems that meet healthcare industry and FDA standards. Our commitment to helping you improve patient outcomes is clear. These innovative features make our products the right choice for you and your patients.Stays in place and diverts away urine to keep skin dryThe PrimaFit®and PrimoFit™ external urine management systems promote early catheter removal, addressing the #1 risk factor of catheter-associated urinary tract infections (CAUTI).All-in-one shampooplus conditioner capThe convenient and pre-moistened fabric-lined caphelps eliminate mess andleaves hair fresh and clean.Contains skin protectantplus cleansers, moisturizers,and deodorizersThe unique dimethicone formulahelps treat and prevent IAD; helpsseal out wetness.Safe in contact with Foley catheters Tested for functional compatibility with common latex and silicone Foley catheters, it also contains a non-antiseptic, pH-balanced solution.Insulated, resealable packagingThe only fully-wrapped, insulated cloth on the market. Washcloths stay warm throughout the bath when warmed in our commercial-grade warmer.Basins were completely eliminated fromtwo medical/surgical units and replaced with Comfort Bath. CAUTI rates were reduced to zero within one month and the rates remained at zero for five months .9On an 18-bed SICU, female patients were identified for early removal of indwelling urinary catheters during daily rounds. PrimaFit was initiated for female patients who remained incontinent after catheter removal.11A 2015 two-phase evaluation of 86 patients at high risk for developing IAD and HAPI found that, in those who received anintervention that standardized incontinence cleanup with a Barrier Cream Clothfollowing each incontinent episode, none developed IAD or a HAPI.10Here’s the proof:*Removing basins reduces CAUTI risk factorsThe impact of using PrimaFit in an effort to address CAUTI prevalenceBarrier Cream Cloth helps prevent IAD and addresses risk factors of hospital-acquired pressure injuries (HAPI)72-year-old patient with severely denuded, blistered skin and extreme pain from incontinence.After using Comfort Shield Barrier Cream Cloths, patient’sskin vastly improved; no discomfort.CAUTIs for5 months 0%IAD orHAPI See thedifference!12CAUTI incidence reduction—73%*Results based on individual hospital and product use. Data provided by facility.Day 1Day 4Product orderingIncontinence Clean-up Cloths (8) Cloths in peel and reseal package8" x 8"30 packages/case Reorder #7505Comfort Shield Barrier Station with removable adhesive strips for wall-mounting near the bedside 24 stations/case Reorder #7599Comfort ShieldBarrier Cream Cloths (3) H eavyweight cloths in easy-tear package8.5" x 8.5"90 packages/case Reorder #7503Medicare ReimbursementHCPCS Code #A6250Comfort ShieldBarrier Cream Cloths (3) H eavyweight cloths in easy-tear package8.5" x 5.5"100 packages/case Reorder #7502Medicare Reimbursement HCPCS Code #A6250Comfort ShieldBarrier Cream Cloths (8) H eavyweight cloths in peel and reseal package8.5" x 9"48 packages/case Reorder #7905Medicare Reimbursement HCPCS Code #A6250Essential Bath ®(8) Medium weight washcloths/package8” x 8”60 packages/case Reorder #7800Comfort Bath Fragrance-free (5) Premium heavyweightwashcloths/package8” x 8”48 packages/case Reorder #7956Comfort Bath ®(8) Premium heavyweightwashcloths/package8” x 8”44 packages/case Reorder #7900Comfort Bath Fragrance-free (8) Premium heavyweightwashcloths/package8” x 8”44 packages/case Reorder #7903Essential Bath Fragrance-free (8) Medium weight washcloths/package8” x 8”60 packages/case Reorder #7803Essential Bath Fragrance-free (5) Medium weight washcloths/package8” x 8”84 packages/case Reorder #7856Baby Comfort Bath Fragrance-free (4) Premium heavyweightwashcloths/package6” x 8”110 packages/case Reorder #7907Clean-up Cloths and Sage PrimaFit External Urine Management System for the Female Anatomy(1) Package of (3) medium weight clean-up washcloths(1) PrimaFit, adult size/package 40 systems/caseReorder #5452Sage PrimaFit External Urine Management for the Female Anatomy (1) PrimaFit, adult size/package 40 devices/case Reorder #5400Sage PrimoFitExternal Urine Management for the Male Anatomy(1) PrimoFit, adult size/package 40 devices/caseReorder #5404HardwareCart31.71" (shelf L) 17.71" (shelf D) 34.63" (cart H)1 cart/case Reorder #793212-Count Warmer 16.89" (H) 14.69" (W)15.24" (D)1 warmer/case Reorder #793728-Count Warmer 18.39" (H) 27.56" (W) 15.39" (D)1 warmer/case Reorder #7939Rinse-Free Shampoo Cap (1) Cap/package 40 packages/case Reorder #7909M-Care ® Meatal Cleansing Cloths (2) Cloths/package5.5” x 8”168 packages/case Reorder #7953Bath Cloths Fragrance-free (8) Standard weight washcloths/package8” x 8”88 packages/case Reorder #7989Bath Cloths Fragrance-free (5) Standard weight washcloths/package8” x 8”78 packages/case Reorder #7959Clean-up Cloths (3) Medium weight washcloths/package6” x 8.5”100 packages/caseReorder #7957Bath Cloths(8) Standard weight washcloths/package8” x 8”88 packages/case Reorder #7982Bath Cloths Fragrance-free (8) Standard weight washcloths/package8” x 8”40 packages/caseReorder #7991Impreva ® Bath Fragrance-free (8) Standard weight washcloths/package8” x 8”88 packages/caseReorder #7988Impreva ® Bath Fragrance-free (5) Standard weight washcloths/package8” x 8”78 packages/caseReorder #7987Return on investmentCost analysisBenchmark and outcome reportS a m p l e r e p o r t000Sample reportOur commitment to youWe believe building partnerships can deliver better outcomes. Our goal is to provide you with the products, training, education, and support you need to provide the best possible care for your patients.Available resources include:Ongoing product and process in-servicing and educationDedicated Medical Science Liaison to discuss evidence-based information with you and your teamPre- and post-intervention assessmentsFocusRN — a clinical education program that includes speaker programs, online learning, and CE modulesEducation through the FocusRN program from clinical thought leadersProtect your pipesThe Traptex ® Plumbing Protection Systemcan help change flushing behavior to stop wipes and non-flushables from entering and clogging your pipes. The result is fewer maintenance calls for clogs, equipment failures, and plumbing disasters.Incontinence Bathing26181F © 2022 Stryker | For use in USASage Products LLC | 3909 Three Oaks Road | Cary, IL 60013 | | 800 323 2220R eferences: 1. Centers for Disease and Control and Prevention (CDC) Urinary Tract Infection (Catheter-Associated Urinary Tract Infection (CAUTI) and Non-Catheter Urinary Tract Infection (UTI) and Other Urinary System Infection (USI) Events. Device-associated Module UTI, 7-1–7-20. January 2020. 2. Toolkit for Reducing Catheter-Associated Urinary Tract Infections in Hospital Units: Implementation Guide, Agency for Healthcare Research and Quality (AHRQ), Rockville, MD. October 2015. 3. Marchaim D, et al., Hospital bath basins are frequently contaminated with multi-drug resistant human pathogens. American Journal of Infection Control 40 (2012) 562-4. 4. Anaisse EJ, Penzak SR, Dignani C, Arch Intern Med. 8 Jul 2002; 162 (13):1483-92. 5. Gray M, Giuliano K, Incontinence-Associated Dermatitis, Characteristics and Relationship to Pressure Injury: A Multisite Epidemiologic Analysis, Journal of Wound Ostomy Continence Nursing, Jan/Feb 2018;45(1):63-67. 6. Health Research & Educational Trust (2017, April). Hospital Acquired Pressure Ulcers/Injuries (HAPU/I): 2017. Chicago, IL: Health Research & Educational Trust. 7. Sage Products LLC. Data on file. Customer Testimonials Home Care. Terms of use available at: https:///store/pg/152-Terms-of-use. Accessed July 29, 2020. 8. Multi-Hospital Sage Products CustomerOne Sponsored Bath Survey June 2019. Accessed June 18, 2019. 9. Stone S, et al., Removal of bath basins to reduce catheter-associated urinary tract infections. Poster presented at APIC 2010, New Orleans, LA, July 2010. 10. Hall, K. and Clark, R. (2015 Jul.). A Prospective, Descriptive, Quality Improvement Study to Decrease Incontinence-Associated Dermatitis and Hospital-Acquired Pressure Ulcers Ostomy Wound Mgmt, 61:(7); 26-30. 11. Beeson T, Davis C, Vollmann KM, Chasing Zero Catheter Associated Urinary Tract Infections (CAUTIs) through Implementing a Novel Female External Urine Collection Device in a Tertiary Academic Surgical Intensive Care Unit (SICU), Oral Abstract, American Journal of Infection Control, 2018:(46);S2-S15. 12. Sluser S, Consistency the key for treating perineal dermatitis due to incontinence. Poster presented at Clinical Symposium on Advances in Skin and Wound Care (SAWC), Las Vegas, NV , Oct 23-26, 2005.Simple interventions.Extraordinary outcomes.We are your partner for proven prevention. Ourmarket-leading products solve real healthcare problems and are backed by clinical evidence. Our products allow you to deliver essential patient care with confidence by addressing risk factors that can lead to infections, skin injury, and caregiver injuries.We are driven to solve real problems and make healthcare better for you and your patients.Find our nurse trusted products at or call 800 490 6493。

P/N 2470HKR (painted) & 2470-1HKR (ceramiccoated) COMPETITION HEADERS1998-02 Camaro, Firebird, Trans AmTo complete (Off Highway) your system, use P/N 16723HKR or 16723-1HKR Y-PipeThank you for making HOOKER HEADERS your choice in a high-performance exhaust system. Extensive dyno/track testing has enabled HOOKER to offer the most advanced design in exhaust systems. The installation, while not complex, will take a certain amount of time. However, the additional horsepower and improved performance will more than justify your efforts. Proper installation and maintenance will ensure long life and maximum performance from your hooker exhaust system.WARNING! Breaking in an engine with ceramic-coated headers WILL result in damage to the coating and will VOID all warranties.Ceramic-coated headers require several heat cycles to fully cure before they will withstand extreme heat. HOOKERrecommends using a cast-iron exhaust manifold or an old header to break in new engines to avoid coating damage.NOTE! These headers do not include provisions for A.I.R. or EGR emissions fittings. They are intended for off-road, closed course racing only and are not designed or intended for street use. Userassumes all responsibility for utilizing these in accordance with state and federal laws. BEFORE STARTINGYour vehicle must be raised a minimum of 36 inches. A floor hoist is ideal. If no hoist is available, we strongly urge the use of axle stands as a safety measure. CAUTION! YOUR CAR SHOULD NOT BE SUPPORTED ON A BUMPER JACK.HELPFUL HINTS FOR HEADER INSTALLATION AND MAINTENANCE1.Verify the header part number with the part number on the box and invoice.2.Unless otherwise noted, Hooker Headers are designed to fit without modifying the header (denting, cutting). DO NOT modify the header.3.Unless other wise noted, Hooker Headers are designed to fit with original equipment (i.e. Oil pan, cylinder heads, mounts, bell housings,starters, etc.).4.When using Hooker Headers, it is recommended to use Hooker gaskets for correct port match. When using other than the recommendedHooker gaskets, match the gaskets to the head ports for a good seal.5.Heat wrapping is not recommended, because it will prematurely fatigue the header.6.Headers that are subjected to extreme conditions (mud, road salt, etc.) should be cleaned on a regular basis to help prevent corrosion.7.When installing the headers, use anti-seize on header bolts and Y-pipe bolts.SPECIAL COMPONENTS NEEDED FOR ASSEMBLY1.Oxygen Sensor Wire Extension(s) 2 each -------- 28” Long (Included with Header)NOTE: These Oxygen Sensor Wire Extensions are made long enough to use either the oxygen sensor with the 8” wire length or the oxygen sensor with the 12” wire length. Any excess wire length after installation should be looped and secured into a non-used and non-heated cavity or pocket.HEADER INSTALLATION PROCEDURE / DISASSEMBLY & ASSEMBLY INSTRUCTIONSPLEASE READ THOROUGHLY & CAREFULLYDISASSEMBLY1.Disconnect the battery. Raise the car and support it with jack stands2.Disconnect & remove the four oxygen sensors. Mark their location, so they may be reinstalled in their proper location.3.Remove the drive-shaft safety brace. Remove the Y-pipe from the vehicle.DISASSEMBLY OF THE LEFT SIDE1.From below, remove the left-side catalytic converter.2.Disconnect and remove the spark plug wires.3.Remove the spark plugs and the left-side exhaust manifold.4.Point the steering wheel straightforward and turn the key to the lock position and remove the key. Remove the steering shaft. Please takenote of G.M. Pt. Notice # 26068010 which states: To help avoid damage and possible malfunction of the air bag, do not rotate the steering shaft with the steering shaft disconnected. See the G.M. service manual before disconnecting.5.Remove the small left-side heat shield / deflector. Remove the oil filterDISASSEMBLY OF THE RIGHT SIDE1.Unbolt and remove the oil dipstick.2.Disconnect and remove the spark plug wires.3.Remove the spark plugs and the right-side exhaust manifold.4.It is not necessary to remove the starter for installation. However, it will allow for better access to the right side #4 spark plug removal andheader bolt installation.ASSEMBLY OF THE LEFT SIDE WITH HEADERNOTE: Use anti-seize on all header bolts and oxygen sensor threads.1. Insert the left-side header through the chassis from below.2. From above, install the gasket.3. Using the supplied 8mm lock washers over the factory exhaust bolts, start all the header bolts prior to tightening, then evenly tighten all theheader bolts to 20-25 ft./lbs.4. Reinstall the steering shaft and tighten the bolt to factory specifications.5. Reinstall the spark plugs and tighten.6. Reinstall the spark plug wires. Check to ensure that they do not contact the header.7. Install the left-side pre-catalytic converter oxygen sensor into the left-side header collector.NOTE: T hese Oxygen Sensor Wire Extensions are made long enough to use either the oxygen sensor with the 8” wire length or the oxygen sensor with 12” wire length. Any excess wire length after installation should be looped and secured into a non-used and non-heated cavity or pocket.8. Reinstall the small left-side heat shield/ deflector and oil filter.ASSEMBLY OF THE RIGHT SIDE WITH HEADER1. Insert the right-side header through chassis from below.2. From above, install the gasket.3. Using the supplied 8mm lock washers over the factory exhaust bolts, start all the header bolts prior to tightening, then evenly tighten all theheader bolts to 20-25 ft./lbs.4. Reinstall the spark plugs and tighten. Reinstall the spark plug wires. Check to ensure that they do not contact the header.5. Reinstall the dipstick and tighten the retainer bolt.6. Install the right-side pre-catalytic converter oxygen sensor into the right-side header collector7. Reinstall the starter (if removed).NOTE: T hese Oxygen Sensor Wire Extensions are made long enough to use either the oxygen sensor with the 8” wire length or the oxygen sensor with 12” wire length. Any excess wire length afte r installation should be looped and secured into a non-used and non-heated cavity or pocket.PRIOR TO FINISHING CHECK LIST1. Inspect the steering shaft for proper installation.2. Check to ensure that no wires will come in contact with the headers.3. Check to ensure that no (l/s and r/s) heat shields come in contact with the headers.4. Check to ensure that any and all electrical connections that were disconnected are properly reconnected.5. Check to ensure that all oxygen sensor wires are looped and secured in a non-used and non-heated cavity or pocket.6. NOTE: Y-PIPE PART NUMBER 16787HKR OR 16787-1HKR IS RECOMMENDED TO BE USED AND INSTALLED WITH THISHEADER P/N 2470HKR OR 2470-1HKR.7. Reconnect the battery. Start the car and check for leaks.。

AX-PH021.Tool componentsA.PH/TEMP KEY:mode switch:Set the mode for PH value,temperature or moisture.B.ON KEY:press the key to start the unit.C.TEST PROBE:can test PH value,moisture and temperature.D.LIGHT SENSOR WINDOW:can induct sunlight intensity of measured environment.E.BACKLIGHT LCD DISPLAY SCREENF.°C/°F OFF KEY:temperature unit switch/power off key:under temperature mode,press the key to selecttemperature unit as°C or°F(original temperature unit:°C).Keep pressing the key for about3seconds to power off.G.PROTECTING BUSHING:Please take the protecting bushing away when using the test probe.Put on the protecting bushing when it is not in use to protect the test probe(accessories).2.Illustration of display screenA.Sunlight intensity display area:9levels:LOW-,LOW,LOW+,NOR-,NOR,NOR+,HGH-,HGH, HGH+,each increasing in amount and quality.LOW-signifies an extremely dim environment.HGH+signifies an extremely bright environment.B.PH function displayC.PH or temperature value display:It shows3.5to9.0for PH value and-9to°C+50°C(16°F to122°F)for temperature.“Lo”or“HH”indicates the value is out of the measurable range.D.Moisture display area:5levels:DRY+,DRY,NOR,WET,WET+,each increasing in wetness.WET+ signifies an extremely wet environment while DRY+signifies an extremely dry environment.E.Temperature function display.F.Low battery display:The symbol will display on the LCD continuously when the battery is low.3.How to use3.1.Battery InstallationOpen the battery compartment door on the back of the tool and plug one9volt block battery onto the battery connector.Put the battery back to the compartment and close the door.3.2.Operation Instructions3.2.1.OPERATION FOR SUNLIGHT MEASUREMENT•Press the ON button to start the unit.•Point the light sensor window toward max light source.•The current light intensity will be showed on the LCD.3.2.2.OPERATION FOR PH VALUE•Switch the PH/TEMP button on the back of the unit to PH position.•Push the probe down as vertically as possible into the soil which needed to be tested.Do not push the probe too near the stem to avoid damage to the plant’s root.•Press ON button to start the unit.•PH value of the tested soil will be displayed on LCD.•Take several readings to confirm your findings.3.2.3.MOISTURE MEASUREMENT•Switch the PH/TEMP button on the back of the unit to/TEMP position.•Push the probe down as vertically as possible into the soil.Do not push the probe too near the stem to avoid damage to the plant’s root.•Press ON button to start the unit.•Moisture of the tested soil will be displayed on LCD.•Take several readings to confirm your findings.3.2.4.TEMPERATURE OF THE SOIL MEASUREMENT•While testing moisture,the temperature of the soil will be displayed on LCD at the same time.•Press°C/°F OFF button to set the unit of temperature is°C or°F.4.Tips•The unit will be automatically off after5minutes disabling for electricity.•The unit only can be used in soil,please don’t place the probe into water or other solutions.•Don’t leave the probe in the soil longer than necessary to avoid the possibility of damage to the probe.•Don’t bend the probe.•Don’t use the probe to break up the soil.•Don’t put the probe near metal objects and be sure to keep the probe away from metal objects.•Wipe the probe clean and dry before taking another test reading and after use.•Before testing,please lightly shine4″-5″(10-12cm)of the probe and any oxides that may have formed on the surface of the metal.•Insure that the probe is wiped clean and the protecting bushing is put on the test probe before storing in order to avoid the oxidation of the probe.•When the unit is withdrawn from the soil,remember not to grasp the probe.•Low battery:“”icon will be displayed on LCD,please replace the new battery.Out of range,the PH value of the unit is3.5to9.0and-9°C to+50°C for temperature.5.Technical specificationsName:4in1Soil Survey InstrumentType:AX-PH02Test objects:Sunlight￿moisture￿PH value￿temperatureTest range:-sunlight(9levels)LOW-,LOW,LOW+,NOR-,NOR,NOR+,HGH-,HGH,HGH+-moisture(5levels)DRY+,DRY,NOR,WET,WET+-PH value(12levels)3.5~9.0(display resolution0.5)-Soil temperature-9°C~+50°C(16°F~122°F)(display resolution1°C/1°F)Automatic off:The unit will be automatically off after5minutes disabling.Backlight function:It will be automatically off within1.5minutesPower supply:One9V block batteryWorking current:<30mAOperating temperature:+5°C~+40°CWorking humidity:5%~95%RH non-condensingStorage Condition:-20°C~+60°C,≤85%(w/o battery)Size:122mm×63mm×36mmTest probe size:φ5mm×200mm Weight:About73g(battery not included)。

ABB-WelcomeM2304Video distributor1Safety (3)2Intended use (3)3Environment (3)3.1ABB devices (4)4Operation (5)4.1Control elements (5)4.2Operating modes (5)5Technical data (9)6Mounting / Installation (10)6.1Requirements for the electrician (10)6.2General installation instructions (11)6.3Mounting (12)1SafetyWarningElectric voltage!Risk of death and fire due to electrical voltage of 100-240 V. – Work on the 100-240V supply system may only be performed by authorised electricians!–Disconnect the mains power supply prior to installation and/or disassembly!2 Intended useThe M2304 video distributor is an integral part of the ABB Welcome door communication system and operates exclusively with components from this system. Device M2304 can be mounted easily inside flush-mounted box, or surface mounted on the wall by one screw.3EnvironmentConsider the protection of the environment!Used electric and electronic devices must not be disposed of with domestic waste.– The device contains valuable raw materials which can be recycled. Therefore, dispose of the device at the appropriate collecting depot.3.1 ABB devicesAll packaging materials and devices from ABB bear the markings and test seals for proper disposal. Always dispose of the packaging material and electric devices and their components via the authorized collecting depots and disposal companies.ABB products meet the legal requirements, in particular the laws governing electronic and electrical devices and the REACH ordinance.(EU-Directive 2002/96/EG WEEE and 2002/95/EG RoHS)(EU-REACH ordinance and law for the implementation of the ordinance (EG)No.1907/2006)4Operation4.1Control elementsFig. 1: Overview of control buttons1234.2 Control elementsA. In a building, a video distributor divides the video signal into 4 branches inconnection with the indoor stations.B.For a residential complex, the video distributor can be used to divide the video signal into 4risers.5 Technical data6 Mounting / InstallationWarningElectric voltage!Risk of death and fire due to electrical voltage of 100-240 V.–Low-voltage and 100-240 V cables must not be installed together ina flush-mounted socket!In case of a short-circuit there is the danger of a 100-240 V load onthe low-voltage line.6.1 Requirements for the electricianWarningElectric voltage!Install the device only if you have the necessary electrical engineeringknowledge and experience.•Incorrect installation endangers your life and that of the user of the electrical system.•Incorrect installation can cause serious damage to property, e.g.due to fire.The minimum necessary expert knowledge and requirements for theinstallation are as follows:•Apply the "five safety rules" (DIN VDE 0105, EN 50110):1. Disconnect from power;2. Secure against being re-connected;3. Ensure there is no voltage;4. Connect to earth;5. Cover or barricade adjacent live parts.•Use suitable personal protective clothing.•Use only suitable tools and measuring devices.•Check the type supply network (TN system, IT system, TT system)to secure the following power supply conditions (classic connectionto ground, protective earthing, necessary additional measures,etc.).6.2 General installation instructions•Terminate all branches of the wiring system via a connected bus device (e.g., indoor station, outdoor station, system device).•Do not install the system controller directly next to the bell transformer and other power supplies (to avoid interference).•Do not install the wires of the system bus together with 100-240 V wires.•Do not use common cables for the connecting wires of the door openers and wires of the system bus.•Avoid bridges between different cable types.•Use only two wires for the system bus in a four-core or multi-core cable.•When looping, never install the incoming and outgoing bus inside the same cable. •Never install the internal and external bus inside the same cable.6.3 MountingDevice M2304 can be easily mounted in the flush-mounted box or surface mounted on the wall by a screw.Mounted with flush-mounted boxMounted on the wallNoticeWe reserve the right to at all times make technical changes as well as changes to the contents of this document without prior notice.The detailed specifications agreed to at the time of ordering apply to all orders. ABB accepts no responsibility for possible errors or incompleteness in this document.We reserve all rights to this document and the topics and illustrations contained therein. The document and its contents, or extracts thereof, must not be reproduced, transmitted or reused by third parties without prior written consent by ABB.。

Pen type, with electrode, ATC PH METERModel : PH-222Your purchase of this PHMETER marks a stepforward for you into thef i e l d o f p r e c i s i o nmeasurement. Althoughthis METER is a complexand delicate instrument,its durable structure willallow many years of useif proper operatingt e c h n i q u e s a r edeveloped. Please readt h e f o l l o w i n ginstructions carefullyand always keep thismanual within easyreach.TABLE OF CONTENTS1. FEATURES (1)2. SPECIFICATIONS (1)3. FRONT PANEL DESCRIPTIONS (4)3-1 Display (4)▲4 3-2 Power ( Logger, ) Button.................................3-3 Hold ( Enter, CAL ) button (4)3-4 REC ( / button, ) Button............................℃℉▼4 3-5 pH electrode ( Temp. sensor ) (4)3-6 Battery compartment/Cover (4)3-7 Protection cover (4)3-8 pH 7.00 buffer solution, PH-07A (4)3-9 pH 4.00 buffer solution, PH-04A (4)4. pH CALIBRATING PROCEDURE (5)4-1 Calibrating Consideration (5)4-2 Requiring Equipment for Calibration (5)4-3 Calibration procedures (5)5.MEASURING PROCEDURE (10)5-1 pH measurement (10)5-2 Data hold (11)5-3 Data record ( Max., Min. reading ) (11)℃℉12 5-4 Change Temp. unit , .................................... 6.DATA LOGGER. (12)6-1 Save data (12)6-2 Call data (13)6-3 Delete data ( Empty the memory ) (14)7. REPLACEMENT OF BATTERY (15)8. REPLACEMENT OF pH ELECTRODE (15)9. OPTIONAL ACCESSORIES (16)*Pen type digital pH meter, all in one, pH electrode is included, easy for general purpose application.*Build in temperature sensor, ATC ( auto temperature compensation ).*pH 4, pH 7 standard solution are standard accessories. *Easy to change the pH electrode.℃℉*Temperature measurement, , .*IP67, water proof and protection.*Auto calibration for pH 4, pH 7 or pH 10 or other value. *High input impedance.*LCD with two displays and bar graph indicator.*Data hold function for freezing the desired value.*Auto power off.*Records max. and min. value with recall.*100 point data logger with recall.*Microcomputer circuit, intelligent function, high accuracy. *Compact size, light weight.*Power supply by DC 1.5 V battery ( UM4/AAA ) x 4 PCs, *Available for wide applications, such as aquarium, beverage, fish hatcheries, food processing, photography, laboratory, quality control, school & colleges, swimming pools, water conditions.Display LCD, size : 20 mm x 28 mm.*With bar graph indicator. Measurement pH0 to 14 pH.℃℉Range Temp.-5 to 80 ( 23 to 176 ). Resolution pH0.01 pH.℃℉Temp.0.1 / 0.1 .Accuracy pH±0.02 pH* After calibration.℃℉Temp.± 0.8 / ± 1.5 .pH Input 10^12 ohms.ImpedapH Electrode Included.* PE-12pH Temp.ATC ( Automatic temperature Compensation compensation ), build thermister Temp.sensor.Data Hold Freeze the display reading.Memory Recall Maximum & Minimum value. Sampling Approx. 0.8 second.TimepH pH 7, pH 4 or pH 10, 3 points Calibration calibration ensure the best linearity andaccuracy.*Other calibration point that near thepH 7, pH 4, and pH 10 are available.Data Logger Max. can save 100 point data with recall.Manual, push the data logger buttononce will save data one time.Circuit Custom one-chip of microprocessor LSIcircuit.:Operating Meter℃℉Temperature0 to 60 ( 32 to 140 ).pH electrode :℃℉-5 to 80 ( 23 to 176 ). Operating Less than 80% RH.HumidityPower Supply DC 1.5V battery ( UM-4/AAA ) x 4 PCs. Power Approx. 4.8 mA.ConsumptionDimension186 x 40 x 32 mm( 7.3 x 1.6 x 1.3 inch ).*Meter with pH electrode.Weight131 g/0.36 LB (included electrode). Power off Auto power shut off to save battery life.Standard Instruction Manual......................... 1 PC Accessories pH electrode, PE-12........................ 1 PCpH 7.00 buffer solution, PH-07A...... 1 PCpH 4.00 buffer solution, PH-04A...... 1 PC* PE-12, PH-07A, PH-04A are theconsumer accessory.Optional pH ELECTRODE, Model : PE-12 Accessories pH 7.00 buffer solution, Model : PH-07ApH 4.00 buffer solution, Model : PH-04AHard carrying case, Model : CA-06Soft carrying case, Model : CA-05A* refer page 163-1 Display▲3-2 Power ( Logger, ) Button3-3 Hold ( Enter, CAL ) button℃℉▼3-4 REC ( / button, ) Button3-5 pH electrode +Temp. sensor, PE-12 3-6 Battery compartment/Cover3-7 Protection cover3-8 pH 7.00 buffer solution, PH-07A3-9 pH 4.00 buffer solution, PH-04A4-1 Calibrating ConsiderationThe pH meter already calibrated by mV signal that simulated from the ideal pH ELECTRODE mV output℃( base on 25 environment ). However due to (a) An ideal electrode will produce 0 mV at pH 7.00, but most electrodes are slightly off. (b) The measuring environment℃℃temperature may not near 25 ( 15 to 35 ).If intend to keep instrument combined electrode within high accuracy, it is necessary to make the following calibration procedures ( 4-3 ).*Basic calibration ( single point calibration ) :pH 7 calibration.*Complete calibration ( two points calibration ) :pH 7 calibration and pH 4 calibration.*During execute the calibration procedures,if the Display show " Error " information, then pleasedo the " Calibration clear " procedures, refer page 8.4-2 Requiring Equipment for Calibration1)Combination pH electrode ( PE-12, included ).2)Buffer solutions :pH 7.00 buffer solution ( PH-07A, included ).pH 4.00 buffer solution ( PH-04A, included ).4-3 Calibration procedures1)Rinse the electrode in distilled water.2)Power on the instrument by pressing the " Power button " ( 3-2, Fig. 1 ).3)Press the " Hold button " ( 3-3, Fig. 1 ) once.the display will show the " HOLD " symbol.▼Press the " button " ( 3-4, Fig. 1 ) once, the display will show following screen in sequence.flashing1)Rinse the electrode in distilled water.2)Power on the instrument by pressing the " Power button " ( 3-2, Fig. 1 ).3)Press the " Hold button " ( 3-3, Fig. 1 ) once.the display will show the " HOLD " symbol.▼Press the " button " ( 3-4, Fig. 1 ) once, the display will show following screen in sequence.flashing▼4)Press the " button " ( 3-4, Fig. 1 ) once, the display will show :screen 34.00CAL5)Place the electrode into pH 4.00 buffer solution ( PH-04A ) Press the " Hold button " ( 3-3, Fig. 1 ) once.The " 4.00 " will flashing, following show " End ".then return the normal measurement screen andfinish the pH 4.00 calibration procedures.flashingDuring execute the calibration procedures, if happen some thing wrong ( Display show Error information ), then execute the following " Calibration clear " procedures will clear all the existing calibration data and return to the Default value.However after execute the " Calibration clear ".then make the calibration again. if the Displaystill show the " Err " ( error information ), thenthe " Standard solution " or the pH electrode "may existing problem.The calibration procedures are :1)Power on the instrument by pressing the " Power button " ( 3-2, Fig. 1 ).2)Press the " Hold button " ( 3-3, Fig. 1 ) once.the display will show the " HOLD " symbol.▼Press the " button " ( 3-4, Fig. 1 ) once, the display will show following screen in sequence.flashing▼3)Press the " button " ( 3-4, Fig. 1 ) once 3 times, the display will show :screen 3CLrCAL5)Press the " Hold button " ( 3-3, Fig. 1 ) once.The " CLr " will flashing, following show " End ". then return the normal measurement screen and finish the " Calibration clear " procedures.flashing5-1 pH measurementAfter the pH electrode is calibrated( section 4-3 ) , the unit is ready for measuring.1)Power on the meter by pressing the " Power button " ( 3-2, Fig. 1 ).2)Place the electrode into the measured solution, little shake the electrode and wait a few seconds to let the ATC ( automatic temperature compensation ) sensor to stabilize with the temperature of the solution.. The LCD will show pH value ( up main display ) and the temperature value ( lower display ) at the same time.3)After make the measurement, please rinse the electrodein distilled water.* After the measurement, the " pH electrode "( 3-5, Fig. 1 ) should insert into the "Protection bottle " ( 3-7, Fig. 1 ).* PE-12, PH-07A, PH-04A is the consumer accessory. 5-2 Data Hold*During the measurement, press the " Hold Button "( 3-3, Fig. 1 ) momentarily to hold the measuredvalue. The LCD will show a " HOLD " symbol.*Press the" Hold Button " once again to release thedata hold function.5-3 Data Record ( Max., Min. reading )1)The data record function records the maximum and minimum readings. Press the " REC Button " ( 3-4, Fig.1 ) momentarily to start the Data Record function,shows " REC " on the display.2)With the " REC " symbol on the display.a)Press the " REC Button " ( 3-4, Fig. 1 ) momentarily,the " REC MAX " symbol along with the maximumvalue will appear on the display.b)Press the " REC Button " ( 3-4, Fig. 1 ) momentarilyagain, the " REC MIN " symbol along with theminimum value will appear on the display.When display shows " REC MAX " or " REC MIN ",*press the " Hold Button " ( 3-3, Fig. 1 )momentarily will delete the max. ( min. ) value,the display will show the " REC. " only andexecute the memory function continuously.c)To exit the memory record function, press the "REC " button for 2 seconds at least. The display willrevert to the current reading, not show " REC "5-4 Change Temp. unit ,℃℉℃℉Press the " / button " ( 3-4, Fig. 1 ) continuously at least two seconds, then release the button will℃℉℉℃change the Temp. unit from to or to .The meter can save max. 100 point data into the the memory circuit6-1 Save data1)Turn on the meter.2)Press the " REC Button " ( 3-4, Fig. 1 ) momentarily, shows " REC " on the display.3)Press the " Logger Button " ( 3-2, Fig. 1 ) momentarily will save one measuring value to memory, display will show :a.The memory position thatsave the recent data.b.The memory left space no.c.a + b = 100For example : 28 + 72 = 1004)To exit the memory data logger ( record ) function, press the " REC " button for 2 seconds at least. The display will revert to the current reading, not show " REC "6-2 Call data1)Turn on the meter.Press the " Hold Button " ( 3-3, Fig. 1 ) momentarily, LCD shows " HOLD ".Following, press the " REC Button " ( 3-4, Fig. 1 ) continuously until display shows following , then release the button.Button "▼No*flashingPress " Hold Button " ( 3-3. Fig. 1 ) will exit the*data call function.6-3 Delete data ( Empty the memory )1)Turn off the meter first.2)Press the " REC Button " ( 3-4, Fig. 1 ) continuously and not release, at the same time press the " Power Button " ( 3-2, Fig. 1 ) momentarily, the display will show following screen, then release both fingers from the buttons.nCLr3)Press " Button " momentarily, display shows :▼yCLr4)Press " Button " ( 3-3. Fig. 1 ) momentarily, the display shows :nuLLCLrNow all the saved data is deleted, memory will empty.1)When the LCD display show " " ,It is necessary to replace the battery. However, in-spec measurement may still be made for several hours after Low Battery Indicator appears before the instruments instrument become inaccurate.2)To replace the battery, rotate and remove the "Battery Cover " ( 3-6, Fig. 1 ), take out the old batteries, install new batteries :DC 1.5V battery ( UM-4/AAA ) x 4 PCs.3)When install the batteries, should make attention the battery polarity.4)After install the batteries, reinstall the battery cover again.1)new unit, refer the Fig. 2 .2)The pH electrode, PE-12 is the standardFig. 2 the working period and the maintenance.3)Rinse the electrode in distilled water afterthe usage.4)" pH Electrode sensing head " pH electrodeshould insert into the PE-12" Protection bottle " if the meteris not used.pH ELECTRODEModel : PE-12General purpose & high quality pH electrode with BNC connector.Range : 1 to 13 pH ( typical 0 to 14 pH ).pH 7.00 buffer solutionModel : PH-07ApH 4.00 buffer solutionModel : PH-04ACARRYING CASE Model : CA-06Hard carrying case.( 280 x195 x 65 mm ).CARRYING CASE Model : CA-05AVinyl soft case.( 260 x110 x 55 mm ).。

SYBR®Green JumpStart™Taq ReadyMix™Catalog Number S4438Storage Temperature –20°CTECHNICAL BULLETINProduct DescriptionSYBR Green JumpStart Taq ReadyMix combines the performance enhancements of JumpStart Taq antibody for hot start PCR with SYBR Green I and the convenience of an easy-to-use ReadyMix solution. Since the ReadyMix solution includes a fluorescent dye and the reagents for PCR, this is the ideal solution for performing high-throughput quantitative PCR. This ready-to-use mixture of SYBR Green I, JumpStart Taq DNA polymerase, 99% pure deoxynucleotides and reaction buffer is provided in a 2×concentrate for ease of use. Simply add 25 µL of the 2×mix to DNA template, primers and water. The JumpStart Taq antibody inactivates the DNA polymerase at room temperature. When the temperature is raised above 70°C in the first denaturation step of the cycling process, the complex dissociates and the polymerase becomes fully active. There are no special preparation or protocol changes required to activate this hot start.Features• The perfect ReadyMix for high throughput, quantitative PCR applications.• SYBR Green I is ideal for quantifying any DNA sequence.1The dye binds to double-strandedDNA and detection is monitored by measuring the increase in fluorescence throughout cycling.• The hot start mechanism, using JumpStart Taq antibody, prevents non-specific product formation and allows assembled PCR reactions to be placed at room temperature up to 2 hours withoutcompromising performance.• Internal Reference Dye is provided for reaction normalization. Maximum excitation of this dye is586 nm and maximum emission is 605 nm.• When performing large numbers of PCR reactions, the SYBR Green JumpStart Taq ReadyMix cansave a significant amount of preparation time,reduce the risk of contamination from multiplepipetting steps, and provide consistent batch-to-batch and reaction-to-reaction performance.ReagentsSufficient for 100 or 500 PCR reactions (50 µL reaction volume)• SYBR Green JumpStart Taq ReadyMix, Catalog Number S9939, containing 20 mM Tris-HCl, pH8.3, 100mM KCl, 7mM MgCl2, 0.4mM eachdNTP (dATP, dCTP, dGTP, TTP), stabilizers,0.05unit/µl Taq DNA Polymerase, JumpStart Taqantibody, and SYBR Green I.• Internal Reference Dye, Catalog Number R4526, 100×dye. Provided in a 0.3 ml vial.Materials and Reagents Required but not Provided • Water, PCR reagent, Catalog Number W1754• Primers• DNA template• Thermal cycler for quantitative PCRStorage/StabilitySYBR Green JumpStart Taq ReadyMix can be stored at 2-8°C for up to 3 months; there is no waiting for the reaction components to thaw. It can also be stored at –20 °C for up to one year. There was no detectable loss of performance after 10 freeze-thaw cycles. Precautions and DisclaimerThis product is for R&D use only, not for drug, household, or other uses. Please consult the Material Safety Data Sheet for information regarding hazards and safe handling practices.2Preliminary ConsiderationsDNA PreparationThe single most important step in assuring success with PCR is high quality DNA preparation. Integrity and purity of DNA template is essential. Quantitative PCR involves multiple rounds of enzymatic reactions and is therefore more sensitive to impurities such as proteins, phenol/chloroform, salts, EDTA, and other chemical solvents. Contaminants can also interfere with fluorescence detection. The ratio of absorbance values at 260 nm and 280 nm gives an estimate of DNA purity. Pure DNA has an A260/A280ratio of 1.8-2.0. Lower ratios indicate the presence of contaminants such as proteins.Primer DesignSpecific primers for PCR should be designed with the aid of primer design software to eliminate the complications introduced with primer-dimers and secondary structures. Lower primer concentrations decrease the accumulation of primer-dimer formation and nonspecific product formation, which is critical in using SYBR Green I dye in quantitative PCR. Magnesium ConcentrationLower magnesium chloride concentrations usually result in the formation of fewer nonspecific products. The ReadyMix solution is provided at a 2×concentration of 7 mM magnesium chloride (final concentration 3.5 mM). A vial of a 25 mM magnesium chloride solution is provided for further optimization of the final magnesium chloride concentration if necessary.Internal Reference DyeA vial of internal reference dye is included for reaction normalization. Maximum excitation of this dye is586nm and maximum emission is 605 nm. Standard instrument settings for ROX reference dye are satisfactory for the measurement of the internal reference dye. This internal reference dye is necessary for ABI Sequence Detection Systems. ControlsA positive control is always helpful to make sure all of the kit components are working properly. A negative control is necessary to determine if contamination is present. A signal in the no template control demonstrates the presence of DNA contamination or primer dimer formation. See Lovatt, et al.,for a thorough discussion of qPCR controls.3Data AnalysisFollow the recommendations of the real time instrument manufacturer to perform quantitative PCR using SYBR Green I dye. Generally, the log of relative fluorescence is plotted against the number of cycles to determine the threshold cycle (C t) or crossing point. The C t value is used to determine the amount of template in each sample. Consider the following points when determining the C t:• C t is the first detectable increase in fluorescence due to PCR product formation• Cycles before the C t are the baseline cycles• The threshold can be adjusted manually• Threshold should always be set using alogarithmic amplification plot• Threshold should be set in the most exponential phase of the reaction, not after reaching theplateau.Melting CurvesPerforming a melting curve analysis at the end of the run will help analyze only the PCR product. Follow the real time instrument manufacturer’s instructions for melting curve analysis. After running a melting curve, any additional runs involving the same PCR product can be done with data collected in an additional detection step to eliminate primer-dimer and other misprimed product signal.Methods of QuantificationStandard CurvesStandard curves are necessary for both absolute and relative quantification. When generating standard curves, different concentrations of DNA (typically five) should be used to generate a standard curve that will bracket the concentration of the unknown. Each concentration should be run in duplicate.Absolute and Relative QuantificationThis product may be used to quantify target DNA using either absolute or relative quantification. Absolute quantification techniques are used to determine the amount of target DNA in the initial sample, while relative quantification determines the ratio between the amount of target DNA and a reference amplicon. The ideal reference amplicon would have invariant, constitutive expression. In practice, a housekeeping gene is chosen for this function, but there are other reference choices which better adhere to the above requirements.43Absolute quantification uses external standards to determine the absolute amount of target nucleic acid. These external standards contain sequences that are the same as the target sequence or which vary only slightly from the target sequence. The primer binding sites of the external standards are always identical to the target sequence. The similarity between the external standard sequence and the target sequence is necessary for amplification efficiencies between the two to be essentially equivalent. Equivalent amplification efficiencies between the target and external standard are necessary for absolute quantification. A standard curve of external standard dilutions is generated and used to determine the concentrations of unknown target samples.Relative quantification calculates the ratio between the amount of target template and a reference template in a sample. The relative amount of gene expression is a common application for relative quantification. The reference gene, usually a housekeeping gene, must not vary in concentration in different experimental conditions or tissue states for relative quantification to be possible. Amplification of the target and reference template dilutions in the sample should be performed in separate tubes. SYBR Green PCR quantification does not allow for multiplexing. If the reference template and the target template have different amplification efficiencies, then two standard curves need to be generated. The ratio of the resulting amounts of target and reference in the sample of interest can then be determined from these two standard curves. If the reference template and the target template have very similar amplification efficiencies, then only one standard curve for the reference template needs to be generated to determine the ratio of the amounts of target and reference in the sample.Determination of PCR Reaction EfficienciesThe PCR efficiency between a reference sample and a target sample is determined by preparing a dilution series for each target. The C t values from either the reference or target is then subtracted from the other. The difference in C t values is then plotted against the log of the template amount. If the resulting slope of the straight line is less than 0.1, the amplification efficiencies are similar.References1.Morrison, T. B., et al., Quantification of Low-CopyTranscripts by Continuous SYBR®Green IMonitoring during Amplification. BioTechniques,24: 954-962 (1998).2.Sambrook, J. et al. Molecular Cloning: A.Laboratory Manual, Third Edition, Cold SpringHarbor Laboratory Press, New York (2000).Catalog Number M82653.Lovatt, A., et al., Validation of Quantitative PCRAssays, BioPharm., March 2002, p.22-32.4.Bustin, S. A., Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems, J. Mol. Endocrinol. 29, 23-9 (2002)4ProcedureNote:Because SYBR Green I binds to all double-stranded DNA, it is important to test primers and cycling conditions to insure that the PCR product is a single band, or the results will be uninterpretable. It is best to insure PCR specificity by checking the reaction on a normal (non-quantitative) thermocycler and analyzing the result using agarose gel separation.2For best results, optimal concentrations of primers, MgCl2,KCl and PCR adjuncts need to be determined. Testing various combinations of primer concentrations (50-1000 nM) is most efficient for primer optimization. If maximum sensitivity is not required and your PCR target is abundant, satisfactory results for SYBR Green based qPCR are often obtained with final concentrations of both primers 200-400 nM.The following procedure serves as a guideline to establish optimal primer concentrations. Further optimization may be necessary due to primer specificity. For more optimization information, please read the qPCR user guide available online at.Note:The use of up to 5% (v/v) dimethyl sulfoxide (DMSO) will not disturb the enzyme-antibody complex. Other co-solvents, solutes (salts) and extremes in pH or other reaction conditions may reduce the affinity of the JumpStart Taq antibody for the Taq polymerase and thereby compromise its effectiveness.A. Optimizing Primer Concentrations1.Prepare and dispense diluted primers (Fig 1).a.Prepare 60 µL of8 µM working solutions of bothforward (fwd) and reverse (rev) primers in the first tubes of 2 separate 8-tube strips.b.Dispense 30 µL of water into tubes 2-5.c.Transfer 30 µL of the 8 µM primer solution fromtube 1 into tube 2. Mix thoroughly by pipetting upand down at least 5 times.d.Repeat transfer and mixing from tube 2 to 3, 3 to4, and 4 to 5.ing a multichannel pipettor, transfer 5 µL fromthe strip-tubes containing diluted fwd primer intothe first 5 wells down columns 1-5 of a 96-wellPCR plate. After adding fwd primer, PCR mix and template, final concentrations of fwd primer will be 1000, 500, 250, 125, 62.5 nM.f.Similarly transfer 5 µL from the strip-tubescontaining diluted rev primer into the first 5 wellsacross rows A-E. After adding PCR mix andtemplate, final concentrations of rev primer will be 1000, 500, 250, 125 and 62.5 nMFig 1: Follow steps 1a –1f using diagram above2.Prepare qPCR master mix:Add reagents below in an appropriate sized DNase-free tube. Mix gently by vortexing and brieflycentrifuge to collect all components at the bottom ofthe tube.*Use 0.1x for ABI 7500 and Stratagene instruments;replace with FITC for BioRad iCycler.3.Aliquot 26 µL master mix into all wells in the PCRplate that contain primers (A1-E5)4.Mix Thoroughly and transfer 18 µL from each ofwells A1 through E5 to wells A8 through E12.ab-d. Dilute fwd primers b-d. Dilute rev primers55.Add 2 µL template DNA (10-50 ng genomic DNAor 0.1-1 ng plasmid) to one set of reactions(columns 1-5) and 2 µL of water to the othercolumns (8-12).6.Mix gently by vortexing and briefly centrifuge tocollect all components at the bottom of the tube. 7.Perform Thermal cycling:Optimal cycling parameters vary with primerdesign and thermal cycler. Consult your thermalcycler manual. It may be necessary to optimizethe cycling parameters to achieve maximumproduct yield and/or quality.Typical cycling parameters for 100 bp –600bp fragments:This protocol has been successfully tested on the following thermal cyclers: Stratagene MX 3000P, BioRad iCycler, MJ Opticon and ABI 7700.8.Evaluate fluorescence plots (∆Rn) for reactionscontaining target nucleic acid (columns 1-5).Primer combinations with the lowest C t and thehighest fluorescence will give the most sensitiveand reproducible assays. B. Procedure for Routine Analysis1.Preparation of a reaction master mix is highlyrecommended to give best reproducibility. Mix all reagents but template in a common mix, using~10% more than needed. Once template isdiluted into the reaction vessel, master mix isaliquoted into the proper tube or plate forthermocycling.* Volume for 50 µL reaction, however component volumes may be scaled to give the desired reaction volumes.** Use 0.1x for ABI 7500 and Stratagene instruments; replace with FITC for BioRad iCycler.2.Mix gently by vortexing and briefly centrifuge tocollect all components at the bottom of the tube.3.Perform Thermal cyclingTypical cycling parameters for 100 bp –600bp6Troubleshooting Guide7NOTICE TO PURCHASER: LIMITED LICENSEUse of this product is covered by one or more of the following US patents and corresponding patent claims outside the US: 5,994,056 and 6,171,785.. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser’s own internal research. No right under any other patent claim (such as apparatus or system claims in US Patent No. 6,814,934) and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser's activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further information on purchasing licenses may be obtained by contacting the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.SYBR is a registered trademark of Molecular Probes, Inc.JumpStart and ReadyMix are trademarks of Sigma-Aldrich Biotechnology LP and Sigma-Aldrich Co.AH,RS,PHC 08/10-1Sigma brand products are sold through Sigma-Aldrich, Inc.Sigma-Aldrich, Inc. warrants that its products conform to the information contained in this and other Sigma-Aldrich publications. Purchaser must determine the suitability of the product(s) for their particular use. Additional terms and conditions may apply.Please see reverse side of the invoice or packing slip.。

ph酸度计(ph/orp-2002)的详细介绍
台湾better酸度计/在线ph/orp计
品牌：台湾better
ph/redox
ph/orp-2002经济型
酸碱度/氧化还原电位变送器仪器以经济实用、操作简便、测量准确著称，广泛应用于污水处理、自来水、纯水系统、化学工业等普通场合。

特点
? 稳定性好? 采用lcd显示视界
? 采用电压稳定、抗扰性强的线性电源
? 主要操作由一个键完成，简单易学
? 可选择4-20ma模拟信号隔离输出
? 适用高输入阻抗的电极
? 特别适用于废水处理系统、纯水系统等过程标准成套配套? ph/orp变送器
? ph/orp电极
? 电极护套管（1米、可选择加长）
? 防雨接线盒（1p65）
? 安装支架（sus316不锈钢）
? 电极信号线（20米、可选择加长）
? 中文说明书
技术参数
型号 model p/horp-2002
测量范围range: 0-14ph、-1000-1000m 精确度 accuracy: 0.01ph、1mv
操作温度 operate temp: -40-60℃
显示方式 display mode: 液晶lcd 信号输出 signal output: 4-20ma
控制动作 control action: on/off
触点容器 control capacity: 250vac 7a 设定点 set point: 2
电源输入 power supply: 220vac 50hz
开孔尺寸 perforate size: 91mm(h)-91mm(w)-110mm(d) 净重 net weight: 0.2kg。

AEROspaceAUTOMOTIVEDEFENSEINDUSTRIALINSTRUMENTATIONSPACETELECOMMEDICAL101, Rue Ph. Hoffmann93116 ROSNY sous BOIS (Paris)Tel.: +33 1 49 35 35 35 - Fax: +33 1 48 54 63 63 E-Mail: info @P.O. Box 202 - 90101 OULU Tel.: +358 407 522 412 E-Mail: infofi @Carl-Zeiss Str. 10 Postfach 200143 D63307 - RÖDERMARK (Frankfurt)Tel.: +49 60 74 91 07 0 - Fax: +49 60 74 91 07 70 E-Mail: infode @Via Concordia, 5 - 20090 ASSAGO MILANO Tel.: +39 02 48 85 121 - Fax: +39 02 48 84 30 18 E-Mail: infoit @ Regional office: RomaHogebrinkerweg 15b - 3871 KM HOEVELAKEN Tel.: +31 33 253 40 09 - Fax: +31 33 253 45 12 E-Mail: infonl @Sjöängsvägen 2 - SE-192 72 SOLLENTUNA (Stockholm) Tel.: +46 844 434 10 - Fax: +46 875 449 16 E-Mail: infose @Ground Floor, 6 The Grand Union Office Park, Packet Boat LaneUXBRIDGE Middlesex UB8 2GH (London)Tel.: +44 1895 425 000 - Fax: +44 1895 425 010 E-Mail: infouk @6825 West Galveston Street CHANDLER, Arizona 85226Tel.: +1 480 682 9400 - Fax: +1 480 682 9403 E-Mail: infousa @N° 390 Yong He Road 200072 - SHANGHAITel.: +86 21 66 52 37 88 - Fax: +86 21 66 52 11 77 E-Mail: infosh @Shibuya-ku Ebisu 1-5-2, Kougetsu Bldg 405 TOKYO 150-0013Tel.: +81 3 3440 6241 - Fax: +81 3 3440 6242 E-Mail: infojp @Flat D, 6/F Ford Glory Plaza, 37-39 Wing Hong Street Cheung Sha WanKOWLOON HONG KONGTel: +852-2959-3833 - Fax:+852-2959-2636 E-Mail: infohk @25 D, II Phase, Peenya Industrial Area BANGALORE 560058Tel.: +91 80 83 95 271 - Fax: +91 80 83 97 228 E-Mail: infoin @For the above countries, please contact the local agent or RADIALL at info @ALSO REPRESENTED INRadiall Navigator ™ is a tool designed to assist our partners and customers that provides instant access to the right information at the right moment. This tool is intended to make sharing information about Radiall products as easy as possible in one single document.With this in mind, we have created Radiall Navigator as a supplemental guide toinformation available in our catalogs and on our website (). We recognize that time is a very limited and valuable asset. We are confident that Radiall Navigator will help users understand our products, terminologies, and references better .JacketDielectric/insulatorCorrugated ($$$$)LengthConnector 1Boot 1Coax cable Marking Sleeve 2Connector 2Length"Pigtail" AssemblyRF Cable AssembliesRight angle onlyNOTE: S = Single Brand D = Dual Brand | For more information about cables manufactured by Radiall, please visit or contact your Radiall sales representative.The following table is intended as a guideline only. For detailed specifications, please refer to the relevant or to the standard cable manufacturer’s specifications. All dimensions are nominal unless otherwise noted.。

Balston ® 0.01 Micron Membrane FiltersBalston Steam andSterile Air Filters for the Food IndustryRemove 98+% of 0.01 micron particlesRemove liquid condensate at thesame efficiency as for solid particles Remo ve essentially all no nvo latile bo iler feedwater chemicalsCo mply with USFDA, USDA, Health Pro tectio n Branch o f Health and Welfare Canada, and 3-A accepted practicesSto p carryo ver o f bo iler feedwater chemicalsClean In Place (CIP) Filtration Sterile Air FiltrationCulinary Quality SteamParker Hannifin Corporation Filt rat ion and Separat ion Division Haverhill, MA 1-800-343-4048Balston ® Steam FiltersBalston Series SR Filters are in full compliance with the requirements of the US Food, Drug and Cosmetic Act.They also meet the regulations for Indirect Food Addi-tives used as Basic Components for Repeated Use Food Contact Surfaces as specified in 21 CFR Part 177, and Current Good Manufacturing Practices, 21 CFR Part 110. These filters have been accepted by the USDA for use in federally inspected meat and poultry plants.Balston Steam Filters are in full compliance with the 3A Accepted Practices (Number 609-04) for producing steam of culinary quality. They are also in full compliance with the requirements of the Health Protection Branch of Health and Welfare Canada.BenefitsBalston Steam Filters eliminate particulate contamination of food products caused by direct contact with dirty steam. Other benefits include: reduction in steam condensate mixing with food products when steam is used for agitating, mixing, or cooking; eliminate taste and odor problems by reducing boiler feedwater carryover; Reduced maintenance requirements.Model 23/75SRModel SP6-23/75SRParker Hannifin Corporation Filt rat ion and Separat ion Division Haverhill, MA 1-800-343-4048Notes:1 Each SP3, SP4, SP6 filter is supplied mounted on a stand.2 Constructed of food grade EPR.3 Each Steam Filter Assembly is supplied with filter cartridges installed.Parker Hannifin Corporation Filtration and Separation Division Haverhill, MA 1-800-343-4048Remove all viable organisms USDA accepted for use in federally inspected Meat and Poultry plants Low pressure dropFull compliance with FDA requirementsBalston ® Sterile Air FiltersBalston grade SA filter cartridges, rated at 99.9999+%efficiency for 0.01 micron particles, is at least 30 times better than the accepted standard for sterile air filters developed by independent research organizations in the U.S. and U.K. (request Bulletin TI-105A for a detailed discussion on Balston filter efficiency rating procedure,and Bulletin TI-935 for an independent test report on Balston Sterile Air Filters). Balston Sterile Air Filters are in full compliance with the requirements of the FDA.Here’s what one of your colleagues found:A Balston sterile air filter assembly, consisting of Models 200X Series, was tested at the University of Massachu-setts, Department of Food Science and Nutrition, under the direction of Professor David A. Evans, Ph.D.“This sterile air system produced commercially sterile air and, to the limits of detection, no viable colonies of microorganisms were found”.- Professor David A. Evans, Ph.D.Model 200X SeriesModel 2104 SeriesModel A15/80Model 2312Model 2206, 2208Parker Hannifin Corporation Filt rat ion and Separat ion Division Haverhill, MA 1-800-343-4048Balston Filter Cartridge and Housing SelectionBalston provides two grades of coalescing filter car-tridges, Grade DXE and Grade BXE. Singly or intandem, these filters satisfy all requirements for remov-ing liquid and solid contaminants from compressed air.These filters are recommended as prefilters in sterile air systems. The Balston Grade SA filter removes bacteria from compressed air. It is the final filter in a sterile air system.1Decide which grade(s) of filter cartridges fits the application (see selection boxes at left).2Select the filter housing with a port size equal to the line size where the filter is to be located.3For a new installation in which the line size has yet to be selected, determine the gas flow rate and pressure at the point where the filter will be located,and then refer to the flow chart on the reverse side of this data sheet. The filter port size must be equal to or larger than the line size (when specified).4If the sterile air filter assembly requires steamsterilization, stainless steel filter assemblies specifi-cally designed for in-line steam sterilization must be used. These assemblies are identified by the RED print in the flow chart on the next page.1Build your own custom filter assembly using the guideline matrix to the left and specify your model number. Example: 1/2" filter with DPI and Auto Drain with Grade DXE Filter = 2104N-1B1-DXE.2Each assembly is shipped with the filter cartridge installed. To order additional filter cartridges, indi-cate the model number of the cartridges, and the grade. Examples 100-12-DXE, 100-12-BXE, or 100-12-SA, etc.How to Select the Filter Cartridge and Hous-ingHow to Order the Filter AssemblyParker Hannifin Corporation Filt rat ion and Separat ion Division Haverhill, MA 1-800-343-4048Notes:1 Two Type A27/80B-SA in parallel required.In installations where the sterile air filter requires steam sterilization, we recommend the following procedures:The steam sterilization pressure should not exceed 60psig. Preferably, it should be held to 40 psig or less. A typical sterilization cycle is 30 psig steam for 30 minutes.Steaming time can be increased as desired without harm to the filter cartridges. The steam flow should not exceed the normal air flow for the unit. To ensure no buildup of condensate in the housing, condensate should be drained from the filter by a condensate drain valve during the steaming process.Steam Sterilization ProcedureThe cleanliness of the steam is an important factor influencing the life of the Sterile Air Filter cartridges.Parker strongly recommends using Model 23 Steam Filters to ensure optimum operating life (see steam filter section of this literature pack).When autoclaving, the Grade SA filter cartridges will tolerate temperatures to 300°F (149°C) in dry gas. Viton or other heat resistant seals should be used in the housing.Parker Hannifin Corporation Filtration and Separation Division Haverhill, MA 1-800-343-4048Parker Hannifin Corporation Filtration and Separation Division Haverhill, MA 1-800-343-4048Remove all viable organismsFull compliance with FDA requirements High flow ratesUSDA accepted for use in federally inspected meat and poultry plantsBalston ®Sterile Air FiltersBalston grade SA filter cartridges, rated at 99.9999+%efficiency for 0.1 micron particles, is at least 30 times better than the accepted standard for sterile air filters developed by independent research organizations in the U.S. and U.K. (request Bulletin TI-105A for a detailed discussion on Balston filter efficiency rating procedure,and Bulletin TI-935 for an independent test report on Balston Sterile Air Filters). Balston Sterile Air Filters are in full compliance with the requirements of the FDA.Here’s what one of your colleagues found:A Balston sterile air filter assembly, consisting of1/4" NPT Models of Grade DX, Grade BX and Grade SA were tested at the University of Massachusetts, Depart-ment of Food Science and Nutrition, under the direction of Professor David A. Evans, Ph.D.“This sterile air system produced commercially sterile air and, to the limits of detection, no viable colonies of microorganisms were found”.- Professor David A. Evans, Ph.D.Model AKC-0280Model AKC-1480Parker Hannifin Corporation Filt rat ion and Separat ion Division Haverhill, MA 1-800-343-4048Notes:1 Vessel is ASME Section VIII, Division 1code stamped for rated pressure. All AKC series housings have CRN registration numbers assigned in all Canadian provinces.2 Maximum operating temperature may be limited by seal material. Consult factory for recommendations at elevated temperatures.3 Filter assemblies are shipped complete with automatic drain, filter cartridges, and differential pressure indicator.Automatic DrainThe maximum operating pressure for the Model 20-211 Automatic Drain is 400psig. Minimum operating pressure is 10psig.Differential Pressure IndicatorThe maximum operating pressure for the Differential Pressure Indicator Model 41-071 is 250 psig. The DPI is sensitive in the range of 0-5 psi.The Automatic Drain and Differential Pressure Indicator are not included with assemblies containing SA cartridges.4 To order filter cartridges, indicate the grade of filter cartridge by placing theappropriate letter after the ordering number.Examples: 5/100-12-DXE, 100-18-BXE,150-19-SA.5 Grades BXE, DXE are available in boxes of 5 and 10 only. Grade SA is available in boxes of 3 and 10.Parker Hannifin Corporation Filtration and Separation Division Haverhill, MA 1-800-343-4048Remove all viable organisms In-line steam sterilization Low pressure dropFull compliance with FDA require-mentsUSDA accepted for use in federally inspected meat and poultry plantsBalston ® Sterile Air FiltersBalston grade SA filter cartridges, rated at 99.9999+%efficiency for 0.1 micron particles, is at least 30 times better than the accepted standard for sterile air filters developed by independent research organizations in the U.S. and U.K. (request Bulletin TI-105A for a detailed discussion on Balston filter efficiency rating procedure,and Bulletin TI-935 for an independent test report on Balston Sterile Air Filters). Balston Sterile Air Filters are in full compliance with the requirements of the FDA.Here’s what one of your colleagues found:A Balston sterile air filter assembly, consisting of 1/4"Models of Grade DX, Grade BX, and Grade SA were tested at the University of Massachusetts, Department of Food Science and Nutrition, under the direction of Professor David A. Evans, Ph.D.“This sterile air system produced commercially sterile air and, to the limits of detection, no viable colonies of microorganisms were found”.- Professor David A. Evans, Ph.D.Model A33B-SAModel A45B-SAModel A27/35B-SA, A27/80B-SASteam Sterilizable Sterile Air FiltersNotes:1 Adaptors are available which convert threaded ports to sanitary type clamp connections.Ordering Information:Part # 73803 1" NPT x 1" SanitaryPart # 73804 1 1/2" NPT x 1 1/2" Sanitary Part # 73805 2" NPT x 2" Sanitary 2 Condensate drain valve required. Supplied by customer.3 Constructed of food grade Viton.4 Maximum pressure ratings are for temperatures to 130°F (54°C). Please consult factory for maximum pressure ratings at elevated temperatures.Steam Sterilizable Sterile Air FiltersRemove all viable organismsIn-line steam sterilizationHigh flow ratesFull compliance with FDA require-mentsUSDA accepted for use in federally inspected meat and poultry plantsBalston® Sterile Air FiltersBalston grade SA filter cartridges, rated at 99.9999+% efficiency for 0.1 micron particles, is at least 30 times better than the accepted standard for sterile air filters developed by independent research organizations in the U.S. and U.K. (request Bulletin TI-105A for a detailed discussion on Balston filter efficiency rating procedure, and Bulletin TI-935 for an independent test report on Balston Sterile Air Filters). Balston Sterile Air Filters are in full compliance with the requirements of the FDA. Here’s what one of your colleagues found:A Balston sterile air filter assembly, consisting of 1/4" Models of Grade DX, Grade BX, and Grade SA were tested at the University of Massachusetts, Department of Food Science and Nutrition, under the direction of Professor David A. Evans, Ph.D.“This sterile air system produced commercially sterile air and, to the limits of detection, no viable colonies of microorganisms were found”.- Professor David A. Evans, Ph.D.Model AKSB-0280-3-SAModel AKSB-1480-SASteam Sterilizable Sterile Air FiltersSteam Sterilizable Sterile Air FiltersNotes:1 Constructed of food grade Viton.2 Vessel is ASME Section VIII Division 1Code stamped for rated pressure.。

© Esselte NV DYMO 2002Esselte •Industriepark-Noord 30 •9100 Sint-NiklaasElectronic LabelmakerInstructions for Use Etiqueteuse électroniqueMode d’emploi Elektronische Labelmaker Gebruikershandleiding XR UK NL FThis product is CE marked in accordance with the CE directive and is designed to conform with the following international standards:Safety – BSEN 60950IEC 950UL 1950- EN 61000-4-2 (1995)- EN 61000-4-3 (1995)- ENV 50204 (1995)- EN 55022 (1994) + amendment 1 (1995)- FCC Class B* Although unlikely, it is possible that abnormal behavior may result from electrostatic discharges. In such cases, should normal operation not resume, follow the relevant procedure as detailed in the trouble-shooting section: No response to keys.The user should avoid directly touching the thermal print head.Esselte is an ISO 14000 registered company. Plastic components of this printer have been marked to enable final disposal in a manner that is sensitive to the environment.£?¿$)&.,-DYMODYMOYou cannot combine different underlining or box settings, or use them with the big font Move the cursor to the required setting withkeys, and press to select.to exit from a menu or cancel anDYMO DYMODYMODYMOU kunt deze verschillende onderstreep- of omkaderopties niet combineren of gebruiken met de grote lettertype (Big Font)-functie. Verplaats de cursor naar de gewenste optietoetsen, en druk op om。