Influenza A virus Neuraminidas
e/NA Antibody, InVivo Block/Neutralizing Antibody-Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody- 询价
- Biogradetech
- 美国
- BGT-ANT-37435
- 2025年07月14日
- ELISA,Neutralization
- Human
企业认证
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
免疫原详情见datasheet，该抗体亚型为：IgG1
- 保存条件：
-2°C-8°C
- 保质期：
1年
- 库存：
100
- 供应商：
艾美捷科技
- 宿主：
Human
- 应用范围：
ELISA,Neutralization
- 抗体英文名：
Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody
- 抗体名：
Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody
Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody，Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody，Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody,Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody
产品名称：Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody-Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody
产品货号：BGT-ANT-37435
产品规格：100ug#1mg
应用类型：ELISA,Neutralization
蛋白别名：Neuraminidase, 3.2.1.18, NA, Influenza Virus (Flu)
Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody-Influenza A virus Neuraminidase/NA Antibody, InVivo Block/Neutralizing Antibody详情见产品datasheet
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文献和实验The neuraminidase-inhibition (NI) assay is a laboratory procedure for the identification of the neuraminidase (NA) glycoprotein subtype in influenza viruses or the NA subtype specificity of antibodies to influenza virus. A serological
virions generally bind to their receptor on susceptible cells (1 ,2 ). The block to infection may occur at any point following adsorption and entry: Studies on the neutralization of influenza virus have shown that its neutralization by certain monoclonal
The Mouse as Model System to Study Host‐Pathogen Interactions in Influenza A Infections
Figure 5. Immunohistochemical staining for viral proteins in infected lungs. C57BL/6J mice were infected intranasally with 2 × 103 FFU of PR8M virus. Serial lung sections were stained with anti‐influenza antibody
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