Ivd Manufacturers Quality Early One Step Cdv-Cpv-Ccv-Gia AG Ivd

Model NO.
JCA018D
Assay Time
5-10 Minutes
Transport Package
Carton
Specification
10Tests/Kit
Trademark
PETX
Origin
Hangzhou
HS Code
38220010
Production Capacity
5000000PCS/Year
Reference Price
$ 0.01 - 17.10
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Product Description

Veterinary Diagnostic Rapid Test for CDV Ag+CAV Ag+CIV Ag +CPIV Ag  Combo Rapid Test ( CDV-CAV-CIV -GIA  Ag ) Ivd Manufacturers Quality Early One Step Cdv-Cpv-Ccv-Gia AG Ivd
 
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 or plasma
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 Canine Adenovirus 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  min utes

PRINCIPLE
The Canine Adenovirus 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 wa s 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 s pecimen , a visible T line  will appears. The C  line  should always appear after a sample is applied, which  indicate s  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.  
  • If serum or plasma specimen, place 3 drops of specimen into the assay buffer tube. Mix them well for use in the assay.
  • 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.

Ivd Manufacturers Quality Early One Step Cdv-Cpv-Ccv-Gia AG Ivd

 

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.

Ivd Manufacturers Quality Early One Step Cdv-Cpv-Ccv-Gia AG Ivd
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Ivd Manufacturers Quality Early One Step Cdv-Cpv-Ccv-Gia AG Ivd
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Veterinary Instruments

PNEUTEC.IT, 2023