Equine Infectious Anemia Virus Antibody Rapid Test
Principle |
Immunochromatographic assay |
Intended use |
Veterinary in vitro diagnostic
1) Auxiliary diagnosis on Canine infection for veterinarians in practice.
2) Precautionary diagnosis for home use, point-of-care and early judgement for pet owners.
3) Study use for researchers. |
Detection time |
5 to 10 minutes |
Specime |
Serum, secretions or spleen |
Storage |
4 to 30 degree centigrade |
Shelf life |
24 months |
Package |
10 rapid tests
10 sterile swabs
10 assay buffer
1 package insert |
Advantages |
1) Good sensitivity and specificity
2) Strong R&D and technical support
3) Stable performance.
4) Friendly to end users |
Relative products |
- Canine CPV-CCV Combo Test
- Giardia Antigen Test |
INTENDED USE
The Equine Infectious Anemia Virus Antibody Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of Equine Infectious Anemia Virus Antibody (EIAV Ab) in horse's serum, plasma, or whole blood specimen.
Assay Time: 5-10 minutes
Specimen: serum, plasma, or whole blood specimen.
PRINCIPLE
The Equine Infectious Anemia Virus Antibody 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 EIAV antigens. If there are anti-EIAV antibodies in the specimen, a visible T line will appears. 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 Equine Infectious Anemia Virus antibodies in the specimen.
TEST PROCEDURE
- Collect horse's fresh whole blood, serum or plasma specimen for use. Immediately apply the testing once collected the specimen.
- Take out the test device from the foil pouch and place it horizontally.
- Place 50μL of serum or plasma specimen or whole blood into an assay buffer tube. Mix well and directly use in the assay.
- Place 3 drops of the diluted specimen into the sample hole of the test card.
- Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.
COMPANY INTRODUCTION
J&G Biotech Ltd is a privately held company located in London, England. J&G Biotech Ltd and its corporates are engaged in the manufacturing and distribution of in vitro diagnostic products for companion animals, livestock, as well as rapid screening food safety test kits for veterinary drug residues, mycotoxins, and food-borne pathogens. The companion animal rapid test kits have a worldwide distribution under the brand PetX. Some innovative immunoassays are developed to work with reader machines for better service to veterinary practitioners.
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