Cdv + Cpv + Ccv + Giardia AG Combo Test for Dog

• Type: Detection Card
• Syringe: None
• Blood Sampling Needle: None
• Breathing Pattern: None
• Animal Anesthesia Machine Control Method: None
• Assay Time: 5-10 Minutes
• Model NO.: JCA046D
• Payment: T/T, Western Union, Paypal
• Sepecification: 10tests/Box
• Certificate: ISO9001
• Transport Package: Carton
• Specification: 10Tests/Kit
• Trademark: PETX
• Origin: Hangzhou
• HS Code: 38220010
• Production Capacity: 5000000PCS/Year

Product Description

Veterinary Diagnostic Rapid Test for CDV Ag+CAV Ag+CIV Ag+CPIV Ag Combo Rapid Test (CDV-CAV-CIV-GIA Ag)

 

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 minutes

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 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. 
• 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.

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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