Epstein Barr(EB) Rapid Tests

Epstein Barr(EB)-IgM antibody

Catalog No.: BG901C

Packing specification
20 test cards/box

Intended Use

This kit is used to qualitatively detect the existence of EB-VCA-IgM antibodies in serum or plasma sample, as an auxiliary diagnostic reagent of EB virus infection in clinical diagnosis. EB virus (epstein-barr virus), known as human herpes virus, are primarily infected through saliva or blood transfusions. EB virus caused 1% of the cancer in global, and 5.6% of all infectious cancer.

Main Constituent
1.Test Card (Coating the recombinant EB-VCA antigen (P18-P23) on T-line, the goat anti-mouse IgG antibody on C-line. 40test cards/box
2.The sample diluents: 1 bottle (5 ml)
3.Product instruction: 1

Storage conditions and the period of validity

Store at 4～30℃, dry places for 24 months. Use test card within 1 hour once open to atmosphere when the humidity is below 60%, or use it immediately if the humidity is higher.

Test Procedure
1.Equipments: 10μL, 20μL, 50μL micropipettes and matched tips
2.Test process: The temperature of the kit and the test sample should be the same with room temperature before test. Place the test card on a dry horizontal work surface. Add 10μL serum or plasma sample into the sample well, then add 20 μ L of sample dilution immediately and 50μL additional sample diluents 5 minutes later. Observe the result in 15-20 minutes after the serum or plasma samples added. The observation is invalid after 20 minutes.

Test results explain

To develop color on C line only: negative; To develop color on both C line and T line: positive; To develop color on T line only: invalid; Not to develop color on both C line and T line: invalid.
Note: Re-detection if the detection result is invalid. The invalid test cards should be dealt as infectious pollutants. The temperature of the kit and the test sample should be the same with room temperature before pre-detection.

Biovantion Inc is independent from international department of Bioneovan Co., Ltd., which established in 2 0 0 5, is an in vitro diagnostic reagents manufacturer engaged in the research, development, production, and focus on clinical testing for infectious diseases, such as Hepatitis virus, Noro virus, Parvo virus test kits, our products include rapid test cassette and Elisa kits.

All our products have been registered in National Medical Products Administration of China, in year 2020 we get Certificate of ISO 13485:2016 – QUALITY MANAGEMENT SYSTEMS FOR MEDICAL DEVICES from SGS. More importantly, we have awarded the registration certificate from National Medical Products Administration for Diagnostic Kit for IgM Antibody to COVID-19 and IgG antibody to COVID-19 during the outbreak in China, and also we developed COVID-19 Antigen test ; Neutralizing Antibody Test, these products selling well all overthe world