factory price for oem sensitive Lyme Disease Antibody Rapid Test for dogs
- Category: >>>
- Supplier: Jiangsu Fusida Biotechnology Co. Ltd.
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Product Overview
Description
Specification
Lyme Disease Antibody Rapid Test | ||||||||
Place of Origin | Taizhou China | Brand Name | FUSIDA | |||||
Use | Vet Diagnosis | Specimen | Serum Plasma | |||||
Shelf life | 18-24 Months | Assay Time | 5 minutes | |||||
Products Description
1st Step
All reagents must be at room temperature before running the assay.
2nd step
Do not remove test cassette from its pouch until immediately before use.
3rd Step
Do not reuse the test kit.
4th Step
Do not use the test beyond its expiration date marked on the foil pouch.
5th Step
The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
What's wrong with the pet lately?
Fever
Anorexia
Vomiting
Diarrhea
Exhausted
Dry nose
For best results, please strictly adhere to these instructions.
1.All reagents must be placed at room temperature before running the
assay.
2.Do not remove test cassette from its pouch until immediately before use.
Do not reuse .
3.Do not use the test beyond its expiration date marked on the foil pouch.
4.The components have been quality control tested as standard batch unit.
5.Do not mix components from different lot numbers.
assay.
2.Do not remove test cassette from its pouch until immediately before use.
Do not reuse .
3.Do not use the test beyond its expiration date marked on the foil pouch.
4.The components have been quality control tested as standard batch unit.
5.Do not mix components from different lot numbers.
Company Profile
JIANGSU FUSIDA BIOTECHNOLOGY CO., LTD was established in 2016 in Taizhou Pharmaceutical City New Area. It is a high-tech enterprise specializing in food safety testing and product research, development, production and sales.
FUSDIA Biotech currently has professional production and technical personnel, devoted to the development and production of rapid diagnostic reagents, existing food safety, pet disease, livestock and poultry disease and other products.In line with the concept of "honesty, professionalism and innovation", the company establishes and improves the product service system to better provide professional services for users.
FUSDIA Biotech currently has professional production and technical personnel, devoted to the development and production of rapid diagnostic reagents, existing food safety, pet disease, livestock and poultry disease and other products.In line with the concept of "honesty, professionalism and innovation", the company establishes and improves the product service system to better provide professional services for users.
Logistics
FAQ
1.What are the limitations of this product?
This reagent is a qualitative screening reagent, which can detect canine parvovirus / canine coronavirus antigen very accurately,but if the sample is insufficient or the antigen concentration is lower than the sensitivity of reagent detection, the doctorshould make the diagnosis after taking into account all the clinical symptoms. An accurate clinical diagnosis should not be based on a single test result.
2.What is the sensitivity and specificity of this product?
Compared with other similar rapid detection cards, the sensitivity of this card was more than 99%, and there was no cross reaction with canine distemper virus, adenovirus and parainfluenza virus with similar symptoms.
3.Are there positive reactions when tested after vaccination?
Because canine parvovirus and canine coronavirus vaccines may be attenuated vaccines, the virus may increase in the body during immunization and may show positive reactions. However, this phenomenon automatically disappeared after 3-10 days of vaccination.However, animals treated with monoclonal antibodies may be false positive for a long time because they produce secondary antibodies against monoclonal antibodies in vivo.
This reagent is a qualitative screening reagent, which can detect canine parvovirus / canine coronavirus antigen very accurately,but if the sample is insufficient or the antigen concentration is lower than the sensitivity of reagent detection, the doctorshould make the diagnosis after taking into account all the clinical symptoms. An accurate clinical diagnosis should not be based on a single test result.
2.What is the sensitivity and specificity of this product?
Compared with other similar rapid detection cards, the sensitivity of this card was more than 99%, and there was no cross reaction with canine distemper virus, adenovirus and parainfluenza virus with similar symptoms.
3.Are there positive reactions when tested after vaccination?
Because canine parvovirus and canine coronavirus vaccines may be attenuated vaccines, the virus may increase in the body during immunization and may show positive reactions. However, this phenomenon automatically disappeared after 3-10 days of vaccination.However, animals treated with monoclonal antibodies may be false positive for a long time because they produce secondary antibodies against monoclonal antibodies in vivo.
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