Find Verified Virus Antigen Rapid Test Suppliers, Manufacturers and Wholesalers

Strengths of antigen rapid test: FAST & EASY (Compared with PCR test) People could RAPIDLY & EASILY be tested as a prerequisite to school attendance, work, or travel. FAST --PCR test - the swab test looks for viral RNA - may take days to perform. --Antigen test might take only 15-30 minutes to complete. EASY --PCR test swabs must be sent to laboratory to be performed by experienced technicians, it requires expensive and specialized equipment and can take days to get result. -- Antigen test can be run in an office or at home in about 15-30 minutes. The sampling process is FAST & EASY and requires very little expertise. Similar tests are done routinely in clinics for influenza all the time.

The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogs feces or vomit specimen. Assay Time: 5-10 minutes The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY The kit can be stored at room temperature (4-30C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight. TEST PROCEDURE -Collect dogs fresh feces or vomit with the cotton swab from dogs anus or from the ground. -Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction. -Take out the test device from the foil pouch and place it horizontally. -Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device. -Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid. INTERPRETATION OF RESULTS -Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague. -Negative (-): Only clear C line appear. No T line. -Invalid: No colored line appears in C zone. No matter if T line appears. PRECAUTIONS -All reagents must be at room temperature before running the assay. -Do not remove test cassette from its pouch until immediately before use. -Do not use the test beyond its expiration date. -The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers. -All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states. LIMITATION Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.

The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogâ??s feces or vomit specimen. Assay Time: 5-10 minutes The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY The kit can be stored at room temperature (4-30�°C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight. TEST PROCEDURE -Collect dogâ??s fresh feces or vomit with the cotton swab from dogâ??s anus or from the ground. -Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction. -Take out the test device from the foil pouch and place it horizontally. -Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device. -Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid. INTERPRETATION OF RESULTS -Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague. -Negative (-): Only clear C line appear. No T line. -Invalid: No colored line appears in C zone. No matter if T line appears. PRECAUTIONS -All reagents must be at room temperature before running the assay. -Do not remove test cassette from its pouch until immediately before use. -Do not use the test beyond its expiration date. -The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers. -All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states. LIMITATION Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.

This product is based on lateral flow immunoassay to detect ALV P27 antigen in avian serum, cloacal swabs, etc.

Monkeypoxvirus (MPXV) is a double-stranded DNA virus, a member of the orthopoxvirus genus within the Poxviridae family. MPXV falls into the same genus category as Cowpox (CPX), Variola (VARV), and Vaccinia (VACV) viruses. Poxviruses cause disease in humans and many other animals; infection typically results in the formation of lesions, skin nodules or disseminated rash. MPXV causes the disease in both animals and humans. It can be transmitted through animal-to human-contact e.g., animal bites, contact with animal bodily fluids etc., human-to-human contact e.g., touching infected lesions, inhalation of respiratory droplets, and eating infected meat that has not been thoroughly cooked. The incubation period for MPXV is typically 7â??14 days, but can range from 5â??21 days. Early onset symptoms of the disease are: swollen lymph nodes, aches and pains, fever and chills, headaches, and extreme fatigue. After 1-3 days, patients develop rashes, which progress to lesions, eventually scabbing over and falling off. The disease usually lasts for around 2-4 weeks. Swollen lymph nodes are typical of monkeypox. However, lesions may be haemorrhagic or coalesce into large bullae. The Monkeypox virus Antigen Rapid Test kit is a rapid test that utilizes a combination of Monkeypox antibody coated colored particles for the detection of Monkeypox antigen in human sample.

Corona Antigen Rapid Test Kits USD 4.85 FOB.

The self testing product is transformed from the professional testing product CLUNGENE COVID 19 Antigen Rapid Test manufactured by Clongene The BfArM has granted the first special approvals according to 11 paragraph 1 of the German Medical Devices Act ( of antigen tests for self administration by laypersons (self tests) for the detection of SARS CoV 2 Our self testing product can be sold and used in Germany Overview of CLUNGENE COVID 1

USA Manufactured, highly accurate, rapid COVID-19 Antigen test. Clinically validated by third-party medical institutions in USA and Europe (Denmark, Poland). The test is highly specific and sensitive (Specificity 100%, Sensitivity 99.1%). Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.

BOSON Rapid Antigen test card

COVID finger prick, rapid antigen test, or rapid test, is a rapid diagnostic test suitable for point-of-care testing that directly detects the presence or absence of an antigen. It is commonly used for the detection of SARS-CoV-2, the virus that causes COVID-19. Rapid tests are a type of lateral flow tests that detect protein, distinguishing it from other medical tests that detect antibodies or nucleic acid, of either laboratory or point-of-care types. Rapid tests generally give a result in 1 to 15 minutes, require minimal training or infrastructure, and have significant cost advantages. NO Lab Required for results.

Product Description - SARS-CoV-2 Antigen Rapid Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet Covid-19 clinical criteria. Product origin - Turkey / Istanbul Key Specifications/Special Features - vitro diagnostic , Rapid Antigen Test Kit, SARS-CoV-2, Covid 19 Minimum Order Size and Packaging details - 500

FDA EUA

It has CE certificate, 25 tests per box, 40 boxes per carton, high accuracy

It has CE certificate, 1T per box, 540 tests per carton; 25T per box, 1000T per carton. high accuracy

Box size: 400 pieces in a box (individual packaging) Size: 70.3*44.9*32.4cm Weight: 15.5kg TGA certification