General Information One-Step Dengue Rapid Test is to detect the NS1 antigens and IgG&IgM antibodies in human blood. Sensitivity : 99.9% Specificity : 99.5 % Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
INTENDED USE THE ONE STEP ANTI-DENGUE (IGM & IGG) TRI-LINE TEST IS A COLLOIDAL GOLD ENHANCED, RAPID IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF ANTIBODIES (IGM & IGG) TO DENGUE VIRUS (DV) IN HUMAN WHOLE BLOOD, SERUM OR PLASMA. THIS TEST IS A SCREENING TEST, AND ALL POSITIVES MUST BE CONFIRMED USING AN ALTERNATE TEST SUCH AS WESTERN BLOT. THE TEST IS INTENDED FOR HEALTHCARE PROFESSIONAL USE ONLY. 25PCS/BOX
The H pylori can be utilized as a rapid screening process for large populations of patients and highly indicated in the early diagnosis of H pylori infection as the immune response can often precede clinical manifestations of disease From a diagnostic point of view, a high serum level specific antibodies against H pylori must be interpreted as an indication of type B asymptomatic gastritis Specification: Specimen:Serum/plasma/whole blood Sensitivity:96% Specificity:90% Packaging:25 cassettes/box, Certificate:CE and ISO 13485 Raw materials is imported from US OEM packaging is available
KOSTEC can supply Korean rapid test kits, which are not only faster and easier in test but alsoprovide accurater test results. Also price is very much attractive! If you have any interest in this test kits, do not hesitate to contact me. Thanks!
Canine brucella ab rapid test is a lateral flow immunoassay for quick detection of brucella canis in serum. Welcome your enquiry! Specifications Specimens: serum Shelf life: 18 months Storage temperature: room temperature(2-30c degree) 10 tests per kit, sealed in foil pouch
Developed by Bioguard, VETlabs Antibiotic Susceptibility test simplifies the complicated procedures of traditional antibiotic susceptibility tests. Skipping the steps of culturing bacteria, the test provides results for veterinarian's reference in only 12-24 hours. It's easy and convenient to use in clinics without outsourcing test.
Product Details: Brand SD Country of Origin Made in India Specimen Serum Shelf Life 24 Months Temperature Storage 30 Degree Celsius Sensitivity 97.6% Specificity 98.0% H.Pylori Helicobacter pylori (H.pylori) is a spiral shaped bacterium and is found in the gastric mucous layer or adherent to epithelial lining of the stomach. H.pylori causes more than 90% of duodenal ulcers and up to 80% of gastric ulcers. Approximately two thirds of the world's population is infected with H.pylori. The immuno- chronomatographic techinques for the detection of antibodies specific to H.pylori has substantially resolved these problems. General Information: SD BIOLINE H.pylori test is a rapid test for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA etc) specific to Helicobacter pylori in human serum plasma or whole blood. Detection of all isotype (IgG, IgM, IgA) antibodies against H.pylori High Accuracy Sensitivity: 95.9%, Specificity: 89.6% Specimen: Serum. Plasma, Whole blood Material provided with this kit are as follows: SD BIOLINE H.pylori test device multi-device Assay diluent
BIOMETRO is an in-vitro diagnostic device manufacturer serving to improve the health and well-being of people around the world. Our effort for the development of medical IVD device based on proprietary Cathodic Electrochemiluminescence (C-ECL) technology, resulted in better clinical and personal healthcare outcomes globally
The Chagas Ab Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with T. cruzi. Any reactive specimen with the Chagas Ab Rapid Test must be confirmed with alternative testing method(s) and clinical findings. Chagas disease is an insect-borne, zoonotic infection by the protozoan T. cruzi, which causes a systemic infection of humans with acute manifestations and long term sequelae. It is estimated that 16-18 million individuals are infected worldwide, and roughly 50,000 people die each year from chronic Chagas disease (World Health Organization)1. Buffy coat examination and xenodiagnosis used to be the most commonly methods2,3 in the diagnosis of acute T. cruzi infection. However, both methods are either time consuming or lack of sensitivity. Recently, serological test becomes the mainstay in the diagnosis of Chagasâ??s disease. In particularly, recombinant antigen based tests eliminate false-positive reactions which are commonly seen in the native antigen tests4-5. The Chagas Ab Rapid Test is an instant antibody test which detects IgG antibodies the T. cruzi within 15 minutes without any instrument requirements. By utilizing T. cruzi specific recombinant antigen, the test is highly sensitive and specific.
Product Details: Number of Reactions(Preps)/Kit : 30 Brand : CTK Biotech Result Time (Rapid Kits) : 20 mins Sample Type : Blood Test Type : Rapid Test CAT No : R0191C The OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
General Information Method: Double Antigens Sandwich Method Sensitivity : 99.5% Specificity : 98.8% Specimen : Serum / Plasma Reading Time : 5- 10 min
1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma. 2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures. 3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens. 4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. Test Procedure Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) prior to testing. 1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible. 2. Place the test device on a clean and level surface. 3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below. 4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes. Interpretation of Results Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is. Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region. Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
INTENDED USE Feline Immunodeficiency Virus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Immunodeficiency Virus antibody (FIV Ab) in catâ??s blood. PRINCIPLE OF THE ASSAY Feline Immunodeficiency Virus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody in the sample. INTERPRETATION OF RESULTS Positive: The presence of both C band and T band, no matter T band is clear or vague. Negative: Only clear C band appears. Invalid: No colored band appears in C zone, no matter whether T band appears. STORAGE The kit can be stored at room temperature (2-30°C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.
Product Details: Number of Reactions(Preps)/Kit :30T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 10 min CAT No : RK019-30 STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes. Easy to use, Easy to read and interpret Discrimination between HIV-1 and HIV-2 antibodies Room temperature storage Performance Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
INTENDED USE The Malaria Gold Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of antibodies including IgG, IgM and IgA to Plasmodium falciparum (Pf) and vivax, ovale, and malariea (Pv.o.m) in whole blood. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with Plasmodium. Any reactive specimen with the Malaria Gold Rapid Test must be confirmed with alternative testing method(s) and clinical findings. REAGENTS AND MATERIALS PROVIDED 1. Each kit contains 25 test devices, each sealed in a foil pouch with three items inside: a. One cassette device. b. One plastic dropper. c. One desiccant. 2. Sample diluent (1 vial, 5 ml) 3. One package insert (instruction for use). MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer 2. Lancing device for whole blood test
Uncut Sheet H. Pylori (H.P)Ab Rapid Test Package:30sheets/pouch Specimen:Whole Blood/Specimen/Serum INTRODUCTION One Step H. Pylori Ab wb /serum/plasma test is a rapid test for the qualitative detection of antibodies specific to Helicobacter pylori in human serum/plasma and whole blood. In this test kit, the H. pylori antigen â?? colloid gold conjugate and specimen moves along the membrane chromatographically to the test region and forms a visible line as the antigenantibodyantigen gold particle complex forms with high degree of sensitivity and specificity. This one step test only takes about 1015 minutes. Test results are read visually without any instrumentation. SPECIMEN COLLECTION & PREPARATION Both whole blood (with or without anticoagulant), serum and plasma specimens can be used with this assay. Simply follow the standard clinical produres to collect whole blood, serum or plasma specimens. If the specimen cannot be tested on the day of collection, store the serum/plasma specimen in a temperature of 28 ºC for up to 72 hours. Stir and bring the specimens to room temperature before testing. Do not freeze whole blood specimens. Do not freeze and thaw the specimen repeatedly. Attention: Specimens and all materials coming in contact with them should be handling and disposed of as if capable of transmitting infection. Avoid contact with skin by wearing gloves and proper laboratory attire. REAGENTS AND MATERIALS SUPPLIED 1. Test kit 2. Specimen diluents in dropper bottle 3. Plastic dropper to dispense sample
Product name:FIV Ab/FeLV Ag Combo Rapid Test Kit MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification:Â ISO9001 Packing: 10pcs/box
The kit uses colloidal gold immunochromatography assay (GICA) to detected antibodies against Brucella in cattle, sheep and goats. The test duration is 10-15 minutes. 20tests/kit
All OBDII functions: 1. Reads and displays I/M monitor status 2. Reads and displays DTCs 3. Erases DTCs(turns off the MIL) 4. Datastream 5. Views freeze frame data 6. Vehicle Information 7. O2 Sensor Test 8. EVAP test Non-OBDII functions: 1. Supports the ENG/AT/ABS/SRS with read DTCs, erases DTCs, and read datastreams for 42 series models (Nissan,Infiniti,Toyota,Lexus,Scion,Honda,Acura,Subaru,Mitsubishi,Suzuki,Isuzu,Hyundai,Kia,Daewoo,Mazda,Ford,GM,Chrysler,Benz,Smart,Sprinter,BMW,Mini,VW,Seat,Skoda,Audi,Opel,LandRover,Jaguar,Volvo,Porsche,SAAB,EUFord,Vauxhall,Peugeot,Citroen,Renault,Dacia,Fiat,Alfa-Romeo,Lancia) Other features: 1. DTC lookup 2. Multilingual 3. Internet updatable and upgradable 4. Prints data via PC 5. DTC Cause/tips 6. Graphs data 7. Playbacks datastream
Infrared Thermometer - Digital Thermometer Forehead - No Contact Forehead Thermometer - Fever Temperature Machine for Accurate Reading - No Touch Thermometer for Adults and Kids IR Thermometer is one of the best thermometer presented by Sign For Safety PRODUCT INFO SFS Industrial Digital Non-contact Laser Infrared IR Thermometer With Back light Display Place of Origin: Mumbai INDIA Brand Name: MultiBrand Model Number: SFS LY-F1 Power Source: Electric Warranty:1 Year After-sale Service:Online technical support Power Supply Mode:Removable Battery Application:Forehead Material:plastic, ABS Shelf Life:1years Quality Certification:ISO13485 Instrument classification:Class II Safety standard: YY/T 0287-2017 IDT ISO 13485: 2016 Type:Digital Infrared Thermometer Reach Medical Level:yes Color:White Display:LCD Display Battery:2*AAA Alkaline Battery Operating Temperature:10�°C ~40�°C Storage Condition Temperature:Humidity 85% Function:Temperature Testing
