SunshinyMed Tech Co. Ltd

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Feline Parvovirus Nucleic Acid Detection Kit

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Feline Panleukopenia (also called feline distemper) is an acute, highly contagious disease of cats caused by feline parvovirus (FPV). Clinical manifestations are characterized by sudden onset of high fever, intractable vomiting, diarrhea, dehydration, circulatory disturbances, and a dramatic decrease in white blood cells. Feline panleukopenia is a big disease threat for cat since it carries a very high mortality rate, particularly in unvaccinated kittens.


Feline Parvovirus (FPV) Nucleic Acid Detection Kit developed by SunshinyMed is suitable for in vitro qualitative detection of feline parvovirus nucleic acid in feces and anal swab samples of affected cats. It aims to quickly and accurately detect common feline parvovirus and assist in the diagnosis and treatment of feline parvovirus infections.




Production Features

Reliable Detection: Reliable detection of Feline Parvovirus Virus (FPV) in cats, fast detection and report in only 45 min (10 min for extraction, 35 min for PCR detection)

Internal Control: The use of internal control system in the kit can effectively prevent false negative results

Stable and Convenient: Freeze-dried type reagent, easy for storage and transportation, also avoiding contamination

Providing Integrated Solution: Provides a rapid test solution that detects FPV with a high degree of sensitivity and specificity

High Precision: The precision values of intra and inter Ct values were all <3%


Product Parameters

Production NameAmpliSunTM Feline Parvovirus Nucleic Acid Detection Kit
UsageVeterinary Diagnostics
Detection MethodReal-Time PCR
Specimen TypeFresh feces or anal swab
Storage Temperature2-30°C
Result Time45 Minutes
Packaging SpecificationIndividually sealed, 4 tests in total.
FormatLyophilized reagent
Shelf LifeUp to Expiration Date Indicated on Package
Sensitivity500 copies/mL
Precision≤5%


How  to use?

Open the PCR tube and pipette 20 μL of extracted nucleic acid from the sample well of the nucleic acid extraction kit into the PCR tube. Close the cap tightly.


Mix the added liquid thoroughly with the solid in the PCR tube (vortex mixer is recommended) until no solid is visible (approximately 10 s). Then, briefly centrifuge for 5 s using a mini centrifuge to ensure all liquid is at the bottom of the PCR tube and no bubbles remain. Finally, place the tube into the PCR instrument for detection.


Materials provided

8 sets of PCR amplification freeze-dried reagents

8 sets of nucleic acid extraction reagents

8 sampling swabs

8 vials of sample preservation solution