Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

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Product Details
Customization: Available
Type: Detection Card
Specimen: Feces
Manufacturer/Factory & Trading Company
Gold Member Since 2020

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Year of Establishment
2016-10-13
Address
1st Floor, Building#1no. 578, 20th Street, Baiyang Subdistrict, Qiangtang District, ...
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
  • Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
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  • Overview
  • Product Description
  • Company Profile
  • Our Advantages
  • Certifications
  • Packaging & Shipping
  • FAQ
Overview

Basic Info.

Model NO.
VD099
Assay Time
5-10 Minutes
Sample
Supply
Delivery Time
3~5days After Get Payment
Storage Temperature
2-30 Degree
Shelf Life
24 Months
Payment
T/T, Western Union, Paypal
Customized
Accpet
Box Size
15cm*10cm*8cm
Packing
80 Boxs/Carton
Carton Size
68cm*44cm*44cm
Transport Package
Carton
Specification
10 Tests per box
Trademark
VET Diagnostix
Origin
China
HS Code
3822190010
Production Capacity
1 Million/ Week

Product Description

Feline Giardia / Tritrichomonas Foetus Antigen Rapid Test
 

Product Description

The Feline GIA-TRF Ag Combo Test is a test cassette to diagnose the presence of antigens against Giardia (GIA) and Tritrichomonas foetus (TRF) in cat's feces specimen.
Assay Time:  5-10 minutes
Specimen: feces
Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
Specimen Feces 
Assay Time 5-10 minutes
Part No. VD099
MOQ 800 test kits
Delivery time 1 week after Get payment
Packing 10 test kits/Packing box
Storage Temperature 2-30°C,DO NOT FREEZE. Do not store the test kit in direct sunlight.
Shelf Life 24 months
Production Capacity 1 Million/Day
Payment T/T, Western Union, Paypal
 

R & D background
Trichomonas fetus is a single-celled, flagellated protozoan parasite that inhabits the colon and terminal ileum of felines. Infected cats may be asymptomatic or may have clinical symptoms, including foul-smelling large bowel diarrhea. T. foetus infection is common in, but not limited to, high-density young purebred cat populations. Testing for this parasite is still not routine in most veterinary clinics, and Trichomonas fetus is often misdiagnosed as Giardia. T. foetus should be considered for specific testing in cats with colorectal diarrhea, especially those for which conventional diagnosis and treatment of other causes of colorectal diarrhea in cats have failed to achieve clinical solutions. Correct identification of T. foetus is essential for the treatment of feline trichomoniasis.


Principle
The Feline Giardia-Tritrichomonas Ag Combo Test is based on sandwich method lateral flow immunochromatographic assay. The test card features two testing windows, each containing a T (test) zone and a C (control) zone that are initially invisible before the assay. When the treated sample is applied, the liquid flows laterally across the NC membrane of each test strip, interacting with pre-coated the antibodies specific to Giardia lamblia, Tritrichomonas foetus respectively. The presence of target antigens in the sample results in a visible T line, while the appearance of the C line indicates a fulfillment of the assay in success.Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

Material Provided
10T Kit 1T Kit
• 10 GIA-TF test cards
• 10 Vials of assay buffer
• 10 Disposable droppers
• 10 Specimen collection swabs
• 1 Instruction for use
• 1 GIA-TF test card
• 1 Vial of assay buffer
• 1 Disposable dropper
• 1 Specimen collection swab
• 1 Instruction for use
Materials Required but Not Provided:
• Timer

Clinical Date
Result RT-PCR Test
Positive Negative
Feline Giardia antigen test Positive 125 4
Negative 2 175
Relative Sensitivity 98.4%
Relative Specificity 97.8%
Relative Accuracy 98.0%
Result RT-PCR Test kit
Positive Negative
Feline Tritrichomonas Foetus Antigen Test Positive 83 8
Negative 7 105
Relative Sensitivity 92.22%
Relative Specificity 92.92%
Relative Accuracy 92.61%

Test Procedures
Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

Before use, all components must equilibrate to room temperature (15 - 25°C) for 10 minutes.
  1. Remove the test card from the foil pouch and place it flat on a work surface.
  2. Transfer 4 drops of the treated sample from the assay buffer tube into the each sample well.
  3. Start the timer. Wait for 5 to 10 minutes to read the result.

Interpretation of Results
- Positive (+): The presence of both "C" line and zone "T" line, no matter T line is clear or vague.
- Negative (-): Only clear C line appear. No T line.
- Invalid: No colored line appears in C zone. No matter if T line appears.

 
Storage And Stability
The kit can be stored at room temperature (2-30°C).
The test kit is stable through the expiration date (24 months) marked on the package label.
DO NOT FREEZE.
Do not store the test kit in direct sunlight.
  
Precautions
- All reagents must be at room temperature before running the assay.
- Do not remove test cassette from its pouch until immediately before use.
- Do not use the test beyond its expiration date.
- The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
- All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states.
The Feline Panleukopenia Virus-Coronavirus-Giardia lamblia Ag Combo Test is for in vitro veterinary use only. Results should be considered alongside other clinical information.
 

Company Profile

Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test
Hangzhou Evegen Biotech Co., Ltd. is an R&D-driven biotech company with a highly experienced technical team specializing in genetic engineering and IVD immunoassay. We have well-established veterinary drug GMP facilities and biosafety level-II laboratories. All production activities are under control of ISO9001. ISO14001 and ISO45001.

Through our global brand VETDiagnostix, we provide rapid, accurate diagnostic solutions for veterinarians treating companion animals, livestock, equine, and exotic species (birds, reptiles, and rabbits). We also offer an easy-to-use rapid test reader for both qualitative and quantitative analysis of lateral flow immunoassay results.

Unlike other industry peers, we maintain complete in-house development of core immunoassay materials, giving us unique control over product quality and innovation. Our scientific team demonstrates industry-leading R&D efficiency, consistently achieving accelerated development cycles without compromising performance. We employ a market-driven approach, focusing on genuine clinical needs to develop tailored, localized diagnostic solutions. Notably, we possess specialized expertise in zoonotic disease diagnostics, with a proven track record of designing high-performance assays for these challenging pathogens.

Our Advantages

Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

Certifications

Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

Packaging & Shipping

Giardia & Tritrichomonas Foetus Antigen Rapid Combo Test

FAQ

Q: Are you trading company or manufacturer?
A: We are a professional manufacturer specialized in veterinary rapid diagnostic test products. And we trade our rapid diagnostic test products with our clients directly.

Q: Can you do OEM and ODM?
A: Yes, OEM and ODM are both acceptable. The material, color, style can be customized, the Minimum Order Quantity we will offer after discussion.

Q: Can we use our own logo?
A: Yes, we can print your own logo according to your request.

Q: How many kinds of packaging methods are available?
A: We have five packaging methods including PE bag, hand bag, zip lock bag, colorful box and white box currently.

Q: Can you make the packaging as we want?
A: Yes, you just provide the package design and we will produce what you want. We also have the professional designer can help you do the packaging design.

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