Buy AccuTest HCV Rapid Card Test (30 Tests) Online from Accurex. HCV means Hepatitis C Virus which is a is a small, enveloped, positive-sense, single-stranded RNA virus. Hepatitis C symptoms are fever, fatigue, decreased appetite, nausea, vomiting, abdominal pain, dark urine, pale feces, joint pain and jaundice. HCV test is a rapid Chromatographic Immunoassay work on principle of the double antigen sandwich technique, Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. AccuTest HCV Test is a rapid Chromatographic Immunoassay for the Qualitative detection of antibodies generated against proteins that are encoded by conserved sequence of core NS3, NS4, NS5 parts of HCV genome in human whole blood/serum or plasma. Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single-stranded RNA virus. Antibody to HCV is found in over 80% of patients with well documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity to increase the sensitivity of HCV antibody tests. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or quest Principle: AccuTest HCV Rapid Hepatitis C Virus Test (Serum/Plasma/Whole Blood) is a lateral flow chromatographic immunoassay based on the principle of the double antigen-sandwich technique. The membrane is coated with recombinant HCV antigen on the test line region of the device. During testing, the serum/plasma or W.Blood specimen reacts with HCV antigen coated particles. The mixture migrates upward on the membrane chromatographically by capillary action to react with recombinant HCV antigen or membrane and generate a colored line. Presence of this colored line indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that the correct volume of specimen has been added and membrane wicking has occurred. Storage and Stability: AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch. Test Procedure: 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Safety Information •Positive: If a distinct purple line is formed at the test one marked ‘T’ (Test Line) and the Control Zone marked ‘C’ (Control Line) the test result is positive, indicating the sample contains Hepatitis C antibody. The interpretation of test results (+ve for hepatitis) remains unchanged even if there is a difference in intensity of color in positive line and control line as is many a time found. •Negative: If a distinct purple line is formed only at the control zone marked ‘C’ (control line) the test result is negative • Invalid: A total absence of color in both © and (T) regions or no colored band appears on the control © region is an indication of procedure error and/or the test reagent has deteriorated. Repeat with a new test kit. Direction for Use Test Procedure 1. Allow the test, specimen and or control to room temperature prior to the testing 2. Remove one test card from the pouch and place it on a clean flat surface 3. Using the dropper provided one drop of serum/plasma or W. blood sample (30ul) then two drops of buffer (40ul) immediately into the sample well. Avoid overflowing 4. Read results within 15 minutes. Strong positive reaction may visible within 5 minutes. Do not read results after 15 minutes. 5. If negative or questionable results are obtained, the HCV infection is suspected, the test should be repeated ona fresh serum specimen. Other Info Storage and Stability AccuTest HCV should be stored at 4-30C. However, the card may be stored at room temperature not exceeding 30C in the original sealed pouch.

Oscar Chikungunya test is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane, for simultaneous and differential detection of Chikungunya specific antibody (IgM/IgG) in human serum/ plasma for diagnosis of Chikungunya infection. For professional use only. Pack Size: 10 Tests Several methods can be used for diagnosis of chikungunya virus infection. Serological tests, such as ELISAs may confirm the presence of IgM and IgG anti-chikungunya antibodies. The virus may also be directly detected in the blood during the first few days of infection by both serological and virological methods (particularly reverse transcriptase–polymerase chain reaction (RT–PCR)). There is no specific antiviral drug treatment for chikungunya. The clinical management targets primarily to relieving the symptoms, including the joint pain using anti-pyretics, optimal analgesics, drinking plenty of fluids and general rest. The joint pain is often very debilitating; it usually lasts for a few days, but may be prolonged for weeks, months or even years--the name “chikungunya” derives from a word in the Kimakonde language, meaning “to become contorted”, and describes the stooped appearance of sufferers with joint pain (arthralgia).

The OnSite Leptospira IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay that can be performed within 15-20 minutes by minimally skilled personnel, and without the use of laboratory equipment. This test is intended to be used for the simultaneous detection and differentiation of IgG and IgM antibodies to Leptospira interrogans (L. interrogans) in human serum, plasma or whole blood. It is intended to be used as a screening test by professionals, and provides a preliminary test result to aid in the diagnosis of infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Recommended for use: Any person presenting with clinical signs or symptoms consistent with acute infection with interrogans including: high fever, headache, chills, muscle aches, vomiting, jaundice, red eyes, abdominal pain, diarrhea, skin rash After exposure to a known contaminated source Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L; Creatinine: 442 μmol/L; Bilirubin: 20 mg/dL; EDTA: 3.4 μmol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L Shelf life: 24 month Individually sealed foil pouches containing: One cassette device One desiccant 5 μL capillary tubes Sample diluent (REF SB-R0101, 5 mL/bottle) One package insert (instruction for use) CTK Products at a Glance Inserts U.S. CDC Leptospira Homepage: About Leptospira WHO: Leptospirosis Fact Sheets

We are the Leading Supplier of Abbe Refractometer Rajdhani. In the Abbe'' refractometer the liquid sample is sandwiched into a thin layer between an illuminating prism and a refracting prism. The refracting prism is made of a glass with a high refractive index (e.g., 1.75) and the refractometer is designed to be used with samples having a refractive index smaller than that of the refracting prism. A light source is projected through the illuminating prism, the bottom surface of which is ground (i.e., roughened like a ground-glass joint), so each point on this surface can be thought of as generating light rays traveling in all directions. A detector placed on the back side of the refracting prism would show a light and a dark region. Over a century after Abbe''s work, the usefulness and precision of refractometers has improved, although their principle of operation has changed very little. They are also possibly the easiest device to use for measuring the refractive index of solid samples, such as glass, plastics, and polymer films. Some modern Abbe refractometers use a digital display for measurement, eliminating the need for discerning between small graduations. However, the user still has to adjust the view to get a final reading. The first truly digital laboratory refractometers began appearing in the late 1970s and early 1980s, and no longer depended on the user''s eye to determine the reading. They still required the use of circulating water baths to control instrument and fluid temperature. They did, however, have the ability to electronically compensate for the temperature differences of many fluids where there is a known concentration-to-refractive-index conversion. Most digital laboratory refractometers, while much more accurate and versatile than their analog Abbe counterparts, are incapable of readings on solid samples. In the late 1990s, Abbe refractometers became available with the capability of measurements at wavelengths other than the standard 589 nanometers. These instruments use special filters to reach the desired wavelength, and can extend measurements well into the near infrared (though a special viewer is required to see the infrared rays). Multi-wavelength Abbe refractometers can be used to easily determine a sample''s Abbe number.

Product Details: Weight 305 g Model No GM-06 Measuring Geometry 60 Degrees Power Supply Batter, 4 X 1.5 VA Display 4 digits backlit LCD Range 0.1 to 200 gloss units We are offering Digital Gloss Meter which is widely used in Floor maintenance, Surface cleaning quality control, Stone and tile gloss measurement, Checking printed matter, Quality control of paint and ink, Polished metal surface , measurement (chrome plating), Inspection of paint protection and waxing, Auto-body paint inspection,Surface inspection of plastic moldings, Evaluation of detergents and washers,Checking masonry and washers, Checking building exteriors. Specifications: Accuracy: ±1.0 gloss unit ( against reference standard ) Resolution: 0.1 gloss unit Repeatability: ±0.5 GU(0 ... 99.9) Measuring Area: mm ellipse Data Memorized: groups Data Output: RS 232 C serial interface Dimensions: Main unit: 156 x67x28 mm Separate Sensor: 58x28x108 mm Weight : About 305g ( including fitted batteries ) Working condition: Temperature range 0 - 40¿¿¿ and Humidity up to 85%.

STANDARD Mentor BT The pain associated with blood drawing has been minimized by using an amount of blood as minimal as 0.3 µl, and the stored results can be transferred to the smart phone app via Bluetooth technology. NFC communication is also available for the convenience of the user.Advantage Minimized pain associated with blood drawing with an amount of blood as minimal as 0.3 µl No coding Blood glucose data transfer using Bluetooth 4.0 and NFC communication technology. Specification Enzyme Glucose Oxidase biosensor Measurement Range 10 - 600mg/dL (0.6 - 33.3 mmol/L) Test Time 5 sec Sample Volume 0.3 µl Hematocrit 20 - 60% Unit mg/dL Memory Up to 500 tests Battery 3V battery (CR2032) Interpretation of results Cat. No. Product Component Note 01GC520 STANDARD™ GlucoNavii® CodeFree® Plus BT Blood Glucose Monitoring System Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device / Check Strip 01GC270 STANDARD™ Mentor BT Blood Glucose Monitoring System Meter, Test Strip (10EA) / Lancet(10EA) / Lancing Device / Check Strip 01GS21 STANDARD™ Mentor Blood Glucose Test Strip STANDARD™ Mentor Test Strip (25EA x 2 bottle)

STANDARD Mentor The pain associated with blood drawing has been minimized because it has been developed to measure accurately even with an amount of blood as minimal as 0.3 µl. About this item Approved Glucometer : FDA and KMFDS Approved, Accuracy Criteria : Its Fulfills EN ISO 15197 : 2015 International Standards. Minimum Blood Sample Needed : 0.3 μl, Memories : Standard Mentor Glucometer allows to save previous and up to 500 test Memories Box Included : Glucometer, 10 Lancets, 10 Strips, 1 Lancing Device, 1 Meter Check Strip, 3V Battery type CR2032, Carrying case, User Instruction Guide, Warranty Card. Pre & Post Meal Mark Alarm, No Coding Glucometer, 99.9% Gold Electrode Strip. Authorized Representative : MT Promedt Consulting GmbH - Altenhofstrasse 80 66386 St. Ingbert Germany. Warranty & Support : Standard Mentor Glucometer comes with Lifetime Warranty and support provided by Standard, For any product queries contact (18001023105). Advantage Minimized pain associated with blood drawing with an amount of blood as minimal as 0.3 µl No coding Accuracy that meets international standards

Item Description The Accu-Chek Softclix lancing device can help make lancing easy. Its rotatable cap offers 11 fixed depth settings for different skin types. Clixmotion technology minimizes any painful side-to-side motion of the lancet, which is why this lancing device is virtually pain-free to use. Benefits and features Virtually pain-free lancing Clixmotion technology controls the lancet’s movement Less side-to-side motion of the lancet means less skin damage Turn the rotatable cap for 11 penetration depth settings for different skin types The Accu-Chek Softclix lancets are precisely manufactured for precise entry Additional specifications Penetration Depth: 11 fixed-depth options, set with the rotatable cap Penetration Range: 0.8 to 2.3 mm Lancing Technology: Clixmotion Technology Weight: 21 g Alternative Site Testing: AST cap provided Needle Diameter: 0.4 mm Gauge: 28 Coating: Silicon How to use the Accu-Chek Softclix lancing device The Accu-Chek Softclix lancing device is small and easy to operate, with one-hand priming and lancing. Pull off the cap. Insert a new lancet into the lancet holder and push it in until it clicks. Press the cap on again until it clicks. Rotate the cap until the desired penetration depth is set. Press the priming button down until it clicks. Press the lancing device firmly against the side of the fingertip. Press the yellow release button. After measuring your blood glucose, pull off the cap and slide the ejector forwards to remove the lancet.

Item Description The Accu-Chek Safe-T-Pro Uno lancing device keeps up with increased safety and hygienic requirements by health authorities, legislators, and health institutions. At the same time, it provides an ergonomic handling, lancing in just 3 milliseconds, and safety features that prevent accidental needle sticks. Its pre-set lancing depth makes it ready to use immediately. Benefits and Features Ready to use with a pre-set depth setting Safe-T-Technology ensures the needle is always safely stored away Stored needle prevents accidental needle sticks Ergonomical and easy to grip for safe handling Hygienic - each lancet can only be used once Beveled needle and small diameter for virtually pain-free blood sampling Equally suitable for right and left-handed use After a single use, the complete lancing device is disposed of Additional specifications Pre-fixed depth setting: Yes Penetration depth: 1.5 mm Needle diameter : 0.36 mm (28 G) Special needle cut: 3-facet cut Siliconized needle: Yes Sterility : 4 years after sterilization Single-use only: Yes Automatic retraction of needle : Yes Recognition of used device : Yes Intuitive handling : Yes How to use the Accu-Chek Safe-T-Pro Uno Simple, 2-step lancing Twist the sterility cap one quarter turn and remove it. Hold the lancing device between your index finger, middle finger, and thumb. Press the lancing device firmly against the chosen puncture site. Using your thumb, press the release button down completely. Move the lancing device away from the puncture site and discard it.