cPL Canine Rapid Tests(FIA) | Canine Pancreatic Lipase (cPL)Rapid Quantitative Test | VETIVD™ cPL 15 minutes to detect results

The cPL test is a fluorescence immunoassay used along with Immunofluorescence Analyzer for quantitative determination of pancreatic lipase concentration in serum, or plasma. This test is used to diagnose and monitor the level of pancreatic lipase in canine.

cPL Reference range:

Result（Tu/ml) Suggestion

≤ 100 Low risk

100 ~ 300 Medium risk

> 300 High risk

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

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PRODUT DETAILS

Advanced Detection Technology
VETIVD™ cPL 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™ cPL Total clinical trial sample: 1134
Positive sample: 652 Negative sample: 482
Specificity＞99.83% Sensitivity＞94.78%

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	√	√	X	√

Language

cPL Canine Rapid Tests(FIA) | Canine Pancreatic Lipase (cPL)Rapid Quantitative Test | VETIVD™ cPL 15 minutes to detect results

Methodology

VETIVD™ Time-resolved immunofluorescence chromatography

Conventional immunofluorescence chromatography

Colloidal gold immunochromatography

Enzyme-linked immunity