IgM antibody Enterovirus 71 EV71 rapid test kit EV 71 antiboday

short description:

Model Number EV71 IgM Packing 25 Tests/ kit, 20kits/CTN
Name Diagnostic Kit for Human Enterovirus 71  ( colloidal Gold ) Instrument  classification Class II
Features High sensitivity, Easy opeation Certificate CE/ ISO13485 
Specimen Serum, Plasma Shelf life Two Years
Accuracy > 99% Technology  Colloidal Gold 
Storage 2′C-30′C Type Pathological Analysis Equipments


Product Detail

Product Tags

Products Parameters

3.EV-71-2
4-(3)
4-(4)

PRINCIPLE AND PROCEDURE OF FOB TEST

PRINCIPLE

The membrane of the test device is coated with anti EV71 antibody on the test region and goat anti rabbit IgG antibody on the control region. Lable pad are coated by fluorescence labeled anti EV71 antibody and rabbit IgG in advance. When testing positive sample, the EV71 antigen in sample combine with fluorescence labeled anti EV71 antibody, and form immune mixture. Under the action of the chromatography, the complex flow in the direction of absorbent paper, when complex passed the test region, it combined with anti EV71 coating antibody, forms new complex.

If it is negative, the sample does not contain enterovirus 71 IgM antibody, so that the immune complex cannot be formed. There will be no red line in the detection area (T). No matter whether Enterovirus 71 IgM antibody exists in the specimen or not, the remaining colloidal gold-labeled mouse anti-human IgM monoclonal antibody and the goat anti-mouse IgG antibody coated in the quality control area (C) binds. Then the agglutinates develop color in the quality control area, and the red line will appear in (C). The red line is the standard appears in the quality control area (C) for judging whether there are enough samples and whether the chromatography process is normal. It is also used as an internal control standard for reagents.

Test Procedure:

1.The samples tested can be whole blood, including venous blood or Peripheral blood. Whole blood cannot be stored after collecting. I should be used soon after collecting.

2.Serum samples are collected aseptically according to standard techniques. Heat-inactivated serum cannot use. It is not recommended to use lipemic, turbid or contaminated serum. Particulate matter in serum. And precipitation will affect the test results, such samples should be centrifuged or filtered before use.

3.The samples tested can be heparin, Sodium citrate or EDTA anticoagulant plasma.

4.According to standard techniques collect sample. Serum or plasma sample can be kept refrigerated at 2-8℃ for 3 days and cryopreservation below -15°C for 3 months.

5.All sample avoid freeze-thaw cycles.

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About Us

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Xiamen Baysen Medical Tech limited is a high biological enterprise which devotes itself to filed of fast diagnostic reagent and integrates research and development, production and sales into a whole. There are many advanced research staffs and sales managers in the company, all of them are have rich working experience in china and international biopharmaceutical enterprise.

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