HCY™ Canine Parainfluenza Virus PCR Detection Kit is a fluorescent quantitative assay for the detection of Canine parainfluenza Virus (CPIV) in plasma, serum, feces and other samples. Specific primers and Taqman probe are designed with the conserved genes of Canine parainfluenza virus (CPIV) and amplified by fluorescent quantitative PCR. Meanwhile, this kit uses GAPDH gene as the internal reference gene, which meets the requirements of indoor quality control in the whole process from sampling, sample purification to on-line testing.
Designed based on the gene sequences of pathogens prevalent in various regions of the world, fully guaranteeing the accuracy and validity of the test;
The primers are designed with special bases to reduce the risk of missed detection due to gene mutation;
Adopting pre-filled freeze-dried microsphere technology for transportation and storage at room temperature;
Easy to use, no need to prepare reagents in advance;
The minimum detection limit is 1 copies/Test;
Clinical sensitivity 100%, specificity 99.11%;
Add internal standard to prevent false negative results and facilitate indoor quality control.
Quality by Design
Eight of the 42 CPIV sequences from China included in NCBI GenBank were compared for homology, and an evolutionary tree was constructed using the Chinese region (MT124463.1) as the reference sequence.
HCY™ Canine Parainfluenza Virus PCR Detection Kit is designed and developed based on the above gene sequences of endemic pathogens in different regions of the world, fully ensuring the test’s accuracy and validity. At the same time, special bases are introduced in the primer sequence synthesis process to reduce the risk of missed detection due to gene mutation.
LoD and PCR Efficiency
Using real clinical samples, the assay was performed after serial gradient dilution, and the results showed good linear characteristics, and the calculated copy number was as low as 10 copies/Test. Calculation of the experimental data set yielded R2=0.9987 and the amplification efficiency E=94.05%.
Sensitivity and Specificity
The HCY™ Canine Parainfluenza Virus PCR Detection Kit was compared to similar commercially available products and tested 135 real clinical samples, of which the sensitivity was 100% and the specificity 99.11%.
Reference Product
Total
Negative
Positive
HCY™ PCR Test Kit
Positive
1
22
23
Negative
112
0
112
Total
113
22
135
Estimated Value
95% Confidence Interval
Sensitivity
100%
81.50%~100%
Specificity
99.11%
94.45%~100%
Cross-reactivity
The HCY™ Canine Parainfluenza Virus PCR Detection Kit was validated against Bartonella, Borrelia Burgdorferi, Toxoplasmosis, Leptospira, Bordetella bronchiseptica, Feline Calicivirus, Feline coronavirus, Feline herpesvirus, Mycoplasma haemofelis, Candidatus Mycoplasma haemominutum and Candidatus Mycoplasma turicensis, Chlamydia Felis, Canine Coronavirus, Canine Herpesvirus, Canine Distempervirus, and Canine Parvovirus, all of which did not cross-react.
“HCY, Health care for you” is our forever mission. We dedicate to offering safe & reliable products and medical services with our global creditable partners. HCY has already supplied to WHO, MAYO clinic, MGI, DDC, Yale University, Qorvo, Quanterix, Thomas Scientific, SD biosensor, Cardinal Health, Cleveland Clinic, Mars Petcare & LumiraDx, etc. in the past years.
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