Feline FPV/FHV/FCV Antibody Triple Test Kit

Catalog Number: MG-CA-R033

TL;DR — The Feline FPV/FHV/FCV Ab is a quantitative fluorescence immunoassay used with a Migibio Immunofluorescence Analyzer. It ships as a 2-year shelf life, an MOQ of 10, and a 10-minute Quick Test result. For clinical interpretation, see Feline Triple Test: FPV, Herpes and Calicivirus.

Applications & Who It’s For

• Veterinary clinics & animal hospitals — same-visit quantitative Feline FPV/FHV/FCV Ab results to support diagnosis and case management.
• Shelters & catteries — intake screening and vaccination or immunity screening where Feline FPV/FHV/FCV Ab is part of the admission panel.
• Breeders & kennels — monitor infection or immunity status in breeding and boarding groups.
• Reference labs & multi-vet hospitals — batch multiple devices on the analyzer for high-throughput reporting.

See also: Feline Triple Test: FPV, Herpes and Calicivirus.

Product Specifications

Attribute	Value
Place of Origin	China
Classification	Specific Reagents
CAT No.	MG-CA-R033
Package	Box
Appearance	liquid
Specification	10T
Storage	Room Temperature
Shelf life	2 years
MOQ	10
Suitable for	Veterinary
Grade	Reagent Grade

Specification

Tests per Box : 10 Catalog Number : MG-CA-R033

Intended Use

The Feline FPV/FHV/FCV Ab test is a quantitative assay used with an Immunofluorescence Analyzer to measure antibodies for feline panleukopenia virus (FPV), feline herpesvirus (FHV), and feline calicivirus (FCV) in serum or plasma.

Clinical Significance

Feline panleukopenia (FPV), feline herpesvirus (FHV), and feline calicivirus (FCV) are the three core pathogens targeted by the standard feline vaccination protocol. Measuring antibody titres against all three simultaneously provides a convenient assessment of vaccination efficacy and immune status.

A single quantitative triple test helps clinicians determine whether a cat has protective immunity, identify animals requiring booster vaccination, and optimise vaccination schedules for multi-cat environments.

Test Principle

This test uses a double antigen sandwich fluorescence method. The intensity of the fluorescent signal indicates the concentration of antibodies, expressed as Tu/ml.

Materials

Provided: 10 sealed pouches with test devices for FPV-Ab, FHV-Ab, and FCV-Ab Desiccant pouch 1 ID Chip Instructions for Use 10 tubes of FPV/FHV/FCV Ab Sample Buffer 10 pipette tips Required But Not Provided: Immunofluorescence Analyzer Timer Pipette (already provided) Centrifuge (typically not needed)

Storage and Stability

Store at 4-30°C until the expiration date. Perform tests at 18-28°C after opening. Use the test within 30 minutes of opening the pouch.

Specimen Collection and Preparation

Use serum or plasma (EDTA recommended). Separate serum or plasma within 3 hours of collection. Use only clear, non-hemolyzed specimens. Store specimens at 2-8°C for up to 72 hours or below -20°C for long-term storage.

Test Procedure

Preparation: Place a Test Device on a flat surface. Insert the ID Chip into the meter and ensure the Test Device lot number matches. Sample Preparation: Mix 20 μl of sample with FPV/FHV/FCV Ab Sample Buffer. Run the Test: Standard Test : Pipette 100 μl of mixed sample into the test device. Select “Standard Test” on the meter, insert the device, and click “Start Test.” Repeat for each test device. Quick Test : Pipette 100 μl of mixed sample into the test device. Select “Quick Test,” start the timer, and let the device sit for 10 minutes. Insert it into the meter and click “Start Test.” Repeat for each test device.

Results

Results appear on the screen. Print results if needed.

Quality Control

The test includes an internal quality control. If it fails, an error message will appear, and you’ll need to use a new Test Device and sample.

Interpretation of Results

FPV-Ab : 4.5–640 Tu/ml FHV-Ab : 5.0–640 Tu/ml FCV-Ab : 5.0–640 Tu/ml Refer to the results table for interpretation based on antibody levels.

Warnings and Limitations

For in vitro diagnostic use only. Do not use if packaging is damaged. Use one pipette tip per specimen. Results may be affected by technical errors or substances in the blood not listed. Each lab should establish its own reference ranges.