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Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG

China Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG, Find details about China Diagnostic, Rapid Test from Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG

Model NO.
JCA018D
HS Code
38220010
Model NO.
JCA018D
HS Code
38220010
Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen ICH CAV AgVeterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG
 
PrincipleImmunochromatographic assay
Intended useVeterinary 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 time5 to 10 minutes
Specimeserum or plasma
Storage4 to 30 degree centigrade
Shelf life24 months
Package10 rapid tests 
10 sterile swabs
10 assay buffer
1 package insert
Advantages1) 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 Infectious Canine Hepatitis Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of Canine Adenovirus type-I antigen (CAV-I Ag) in secretions from dog's eyes, nasal cavities, and anus or in serum, plasma specimen. 
Assay Time:  5-10 minutes

PRINCIPLE
The Infectious Canine Hepatitis 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 CAV-I antigen 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 CAV-I virus antigen in the specimen.

TEST PROCEDURE
  • Collect dog's ocular, nasal or anus secretions with the cotton swab and make the swab wet sufficiently.
  • 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 "S" of the test device.
  • Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid
  • Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG


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.

Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG
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Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG
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Veterinary Diagnostic Rapid Test for Infectious Canine Hepatitis Antigen Ich Cav AG

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