cProgesterone Canine Rapid Tests(FIA) | Canine Progesterone (cProgesterone) Rapid Quantitative Test | VETIVD™ cProgesterone 10 minutes to detect results

The cProgesterone test is a fluorescence immunoassay used along with Immunofluorescence Analyzer for quantitative determination of progesterone concentration in canine serum or plasma specimen.

cProgesterone Reference range:

Result（Tu/ml) Suggestion

≤ 1.0 Non-estrus phase

1.0 ~ 5.0 Preovulation phase

5.0 ~ 10.0 Oviposit phase

10.0 ~ 20.0 The best potential fertility phase

> 20.0 Ootid senescence phase

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™ cProgesterone 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™ cProgesterone Total clinical trial sample: 1148
Positive sample: 536 Negative sample: 612
Specificity＞99.86% Sensitivity＞94.85%

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

cProgesterone Canine Rapid Tests(FIA) | Canine Progesterone (cProgesterone) Rapid Quantitative Test | VETIVD™ cProgesterone 10 minutes to detect results

Methodology

VETIVD™ Time-resolved immunofluorescence chromatography

Conventional immunofluorescence chromatography

Colloidal gold immunochromatography

Enzyme-linked immunity