Promotioal Hospital Canine Brucella Antibody Rapid Test Device

China Promotioal Hospital Canine Brucella Antibody Rapid Test Device, Find details about China Diagnostic, Rapid Test from Promotioal Hospital Canine Brucella Antibody Rapid Test Device

Model NO.
JCA018D
HS Code
38220010
Model NO.
JCA018D
HS Code
38220010
Veterinary Diagnostic Rapid Test for Canine Brucella Antibody(C.Brucella Ab)Promotioal Hospital Canine Brucella Antibody Rapid Test Device
 
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 Canine Brucella Antibody Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of Canine Brucella Antibody (C.Brucella Ab) in dog's serum, plasma, or whole blood.
Assay Time:  5-10 minutes
Specimen: serum, plasma, or whole blood.

PRINCIPLE
The Canine Brucella 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 Brucella LPS antigens. If there are anti-Brucella antibodies 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 Canine Brucella antibodies in the specimen.

TEST PROCEDURE
  • Collect dog'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 20μL of serum or plasma specimen into an assay buffer tube. Mix well and directly use in the assay.
  • Place 2-3drops (approx.60-80μL) of assay buffer into the sample hole.  
  • Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.

 

Promotioal Hospital Canine Brucella Antibody Rapid Test Device

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.

Promotioal Hospital Canine Brucella Antibody Rapid Test Device
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Promotioal Hospital Canine Brucella Antibody Rapid Test Device
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Promotioal Hospital Canine Brucella Antibody Rapid Test Device