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  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results

CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results

The CPV-Ab test is a fluorescence immunoassay used along with Immunofluorescence Analyzer for quantitative determination of parvovirus antibody concentration in serum or plasma. The test can provide a reference for the level of CPV-Ab titer after vaccination of pets and suggest whether it is necessary to vaccinate them again. Another use of the test is an aid in the diagnosis and monitoring of canine parvovirus  infection.

CPV-Ab Reference range:

Result(Tu/ml)                       Suggestion

        ≤ 9                                    No antibody protection, vaccination recommended.

    9~ 150                               The antibody protection is weak, so it is recommended to carry
                                              out supplementary immunization or adjust the immunization program

 150 ~ 500                            Moderate antibody protection, strengthen antibody level monitoring,
                                             once every 6 months or so.

     > 500                               The antibody protection is strong, and the antibody level is tested
                                             every year to know the vaccine protection in time.

Each laboratory should establish a reference range that is representative of the population to be evaluated.

  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
  • CPV-Ab Canine Rapid Tests(FIA) | Canine Parvovirus Antibody (CPV-Ab) Rapid Quantitative Test | VETIVD™ CPV-Ab 10 minutes to detect results
PRODUT DETAILS

Advanced Detection Technology

VETIVD™ CPV-Ab Rapid Quantitative Test utilizes the cutting-edge third generation
time-resolved immunofluorescence chromatography technology. It employs rare earth element
europium (Eu3+) coated nano-fluorescent microspheres as a distinctive marker, and swiftly
achieves quantitative analysis by analyzing the fluorescence intensity of both the detection zone
and quality control zone.


Third generation time-resolved immunofluorescence chromatography
(double antigen sandwich method)


Rigorous clinical trials
At VETIVD™, we conduct over 500 clinical trials for each product in collaboration with veterinary
university laboratories to ensure that the effectiveness of each product meets thebest standards.

VETIVD™ CPV-Ab Total clinical trial sample: 1303
Positive sample: 481       Negative sample: 822

Specificity>99.85%    Sensitivity>94.76%


Innovative technical support
The VETIVD™ Rapid Quantitative Test utilizes an innovative QR code design in conjunction with
an intelligent identification system to automatically discern sample types, information, and
production batches.


User feedback data display
95% of veterinarians believe
Error rate reduced to 0%

Smart and convenient

Excellent  stability
VETIVD™ employs novel stabilizers, protectants, and cutting-edge packaging technology to
ensure consistent reagent performance across diverse environments.

Tested for long-term storage and transportation
Storage in 4~30℃ environment

 Performance change rate within 2 years is less than 0.03%


Simple detection process
The testing process of VETIVD™ Rapid Quantitative Test has been meticulously optimized,
resulting in a streamlined clinical testing procedure consisting of only 7 steps. This ensures that
users are provided with a diagnostic solution that is both convenient and highly efficient.



Strict quality control
The VETIVD™ brand boasts a state-of-the-art GMP production workshop spanning 5,000 square
meters. From meticulous R&D to precise manufacturing processes, we meticulously select
premium-grade raw materials and enforce stringent quality control measures at every stage,
ensuring unparalleled excellence in our products.



Performance comparison of 4 technology platforms

Methodology
VETIVD™ Time-resolved immunofluorescence chromatography
Conventional immunofluorescence chromatography
Colloidal gold immunochromatography
Enzyme-linked immunity
Marker Nano europium fluorescent microspheres Fluorescein Colloidal gold Enzyme
Qualitative or quantitative Full quantitation Quantify Qualitative semi-quantitative
Kit components 1-2 kinds 1-2 kinds 1-2 kinds 7 kinds
Steps Step 1-2 Step 1-2 Step 1-2 Step 10-15
Sensitivity higher lower low high
Detection time 3-10 minutes 10-15 minutes 15 minutes 120 minutes
Specificity Excellent Normal Normal Normal
Storage method 4-30℃ 2-8℃ 4-30℃ 2-8℃
Epidemic monitoring

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