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Feline panleukopenia IgG Antibody ELISA

Feline panleukopenia IgG Antibody ELISA Kit

Product Code
KE0018
Kit Principle
ELISA

Categories

Applications

This Feline panleukopenia IgG Antibody ELISA Kit is based on an enzyme-linked immunosorbent assay to detect panleukopenia virus  (also known as feline parvovirus ) specific antibodies in feline serum and plasma, moreover, it can be used in the supervision of FPV vaccine antibody levels in cats.

Feline panleukopenia (FP) is a highly contagious viral disease of cats caused by the feline parvovirus. Kittens are most severely affected by the virus. The names feline distemper and feline parvo should not be confused with canine distemper or canine parvo— although their names are similar, they are caused by different viruses. The viruses do not infect people. The feline parvovirus infects and kills cells that are rapidly growing and dividing, such as those in the bone marrow, intestines, and the developing fetus.    

Key facts of the Feline panleukopenia IgG Antibody ELISA Kit

  • Ready to use kits for lab staff
  • No special instrument required
  • Result visible in 60min

Application of the Feline panleukopenia IgG Antibody ELISA Kit

This kit shall be used to test FPV-specific antibodies in feline serum and plasma.

Technical information of Feline panleukopenia IgG Antibody ELISA Kit

Product name Feline panleukopenia IgG Antibody ELISA Kit
Product code KE0018
Test type Qualitative
Principle Indirect immunoassay
Species Feline
Specificity >95%
Sensitivity >95%
Shelf-life 12 months
Storage 2-8 oC
Approval This product was approved by Chinese Ministry of Agriculture

Feline panleukopenia IgG Antibody ELISA Kit Components

  • Precoated microtiter plate, 96wells
  • Negative control
  • Positive control
  • Enzyme conjugate
  • 20xWash buffer
  • Sample buffer
  • Stop solution
  • Kit manual

Further Reading

 

Frequently asked questions

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For certain products, we also have international certifications such as AOAC performance tested method (PTM), ILVO validation, or WOAH reference laboratory validation.

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