Hypersensitivity: After the organism, initial response to certain
antigens, the immune response is enhanced when re-exposure to the
same antigen. When high antigen intake or organism immune response
is in a high level, due to the immune response is too strong, it
will cause specific immune response (mainly tissue injury). In1966,
Ishizaka found and proved that IgE antibody is the major antibody
mediated type I hypersensitivity. Since then, Screen the allergen
through detection of the specific IgE in the serum is an important
diagnosis method of allergic diseases. This kit is used to
qualitatively detect specific IgE antibody and mainly used for the
diagnosis of allergen screen.
Product details
Description
Delivery
Within 48 hours
Packaging Specifications
25 tests/box
Country Of Origin
China
Manufacturer
24months
Preservation method
2℃-30℃
Specimen
urine
Assification
class1
Type
Reply Test
Sample Request
1. To collect the venous blood by conventional method and separated
the serum or plasma as soon as possible to avoid hemolysis.
Hemolysis is not suitable for the test kit.
2. Samples can be stored at 4 ℃ if tests will be done within 7
days, otherwise stored at -20 ℃. No more than 3 times of
freeze-thaw with test sample.
3. The common heparin or sodium citrate anticoagulant does not
influence the test results.
Storage
Store as packaged in the sealed pouch at 4-30°C, avoid hot and
sunshine, dry place, valid for 24 months.
DO NOT FREEZE. Some protective measures should be taken in hot
summer and cold winter to avoid high temperature or freeze-thaw.
Company Profile
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
For Laboratory Or Hospital High Accuracy For Allergen Specific IgE Antibody Rapid Test Kit