Abnova/COVID-19 Human IgM IgG Rapid Test/1kit/DC0301
市场价：
¥0.00
美元价：
0.00
联系Q Q：
3392242852
电话号码：
4000-520-616
电子邮箱：
info@ebiomall.com
商品介绍
- Specification
- Product Description:
- COVID-19 Human IgM IgG Rapid Test provides a fast, convenient, and qualitative testing of human whole blood, serum and plasma for COVID-19 (SARS-CoV-2) IgM and IgG.
- Supplied Product:
- 20 Test Kit:Testing Strips (20)a. Colloidal Gold-Labeled COVID-19 Nucleocapsid (N) Proteinb. Colloidal Gold-Labeled COVID-19 Receptor-Binding Domain (RBD) Proteinc. Colloidal Gold-Labeled Chicken IgY Antibody with less than 0.1% Sodium Azided. Goat Anti-Human IgM Antibodye. Goat Anti-Human IgG Antibodyf. Goat Anti-Chicken IgY Antibody with less than 0.1% Sodium AzideSample Buffers (20)
- Storage Instruction:
- Store product at 15-30°C and avoid direct exposure to sunlight.Do not open until ready to use.Do not freeze or store the product outside the temperature range described above.Do not use after the expiration date.
- Note:
- Product Image
Venous Whole Blood, Serum and Plasma Test Procedure
Finger Prick Whole Blood Test Procedure
- Suitable Sample:
- Human Venous Whole Blood (dipotassium EDTA, sodium heparin, sodium citrate), Serum, Plasma (dipotassium EDTA, sodium heparin, sodium citrate), and Finger Prick Whole Blood (dipotassium EDTA, tripotassium EDTA, no anticogulant)
- Features:
- Fast result in 15 minutesEasy to operateHighly sensitive via visual inspection
- Intended Use:
- This product is a lateral flow chromatographic immunoassay for rapid, qualitative detection of human IgM and IgG antibodies against COVID-19 virus in human venous whole blood (dipotassium EDTA, sodium heparin, sodium citrate), serum, plasma (dipotassium EDTA, sodium heparin, sodium citrate), and finger prick whole blood (dipotassium EDTA, tripotassium EDTA, no anticogulant).
- Regulatory Status:
- GMP gradeCE-IVD approved
- Factsheets:
Fact Sheet for Healthcare ProvidersFact Sheet for Patients
- Adverse Events:
- Reporting adverse events
- Notification:
- Clinical laboratories must include this information in their patient test report as specified in FDA guidance:This test has not been reviewed by the FDA.Negative results do not rule out SARS-CoV-2 infection, particularly in those who have been in contact with the virus. Follow-up testing with a molecular diagnostic should be considered to rule out infection in these individuals.Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status.Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.
- COA:
- COA Download
- InstructionsFor Use:
- Instructions For Use (CE-IVD)Instructions For Use (CE-IVD)(German)Instructions For Use (pre-EUA)Instructions For Use (Japanese)
- Datasheet:
- Download
- Video:
- Applications
- Lateral Flow Immunoassay
- Result zone of the COVID-19 Testing Strip indicates human IgM line (M line), IgG line (G line) and control line (C line). C line must appear to ensure the quality of sample processing. Please refer to the diagram below for interpretation.
- Lateral Flow Immunoassay
- 31 known COVID-19 positive and 75 known negative EDTA whole blood samples were collected, confirmed with EUA authorized RT-PCR, and tested for COVID-19 IgM and IgG reactivity following symptom onset with results read by two blinded, independent viewers.
- Application Image
- Lateral Flow Immunoassay
- enlarge
- Lateral Flow Immunoassay
- enlarge
品牌介绍
Abnova是世界上最大的抗体制造商。亚诺法的所有产品，重组蛋白和抗体都是利用最新的技术及由SPF等级动物实验室制造生产出来。我们的目标是生产人类基因组内每个基因至少要有一个相对应的抗体，可以提供给来自于学术机构、行业的伙伴和合作者做研究。亚诺法有许多多样化的单克隆及多克隆抗体，我们更进一步开发一系列的整合系统与相关应用包含配对抗体、ELISA试剂盒与荧光原位杂交(FISH)探针。这些工具对生物标记开发与转译研究都是必须的。亚诺法亦有针对糖尿病、传染疾病与癌症的体外检验试剂专案以及用于治疗败血症的全人类抗体药技专案，为全人类的健康努力。
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