A型流感病毒H3N2-M2蛋白抗体

Quantity size:

0.2ml

Concentration:

1mg/ml  A型流感病毒H3N2-M2蛋白抗体 Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Background:

Influenza A virus is a major public health threat. Novel influenza virus strains caused by genetic drift and viral recombination emerge periodically to which humans have little or no immunity, resulting in devastating pandemics. Influenza A can exist in a variety of animals;A型流感病毒H3N2-M2蛋白抗体 however it is in birds that all subtypes can be found. These subtypes are classified based on the combination of the virus coat glycoproteins hemagglutinin (HA) and neuraminidase (NA) subtypes. During 1997, an H5N1 avian influenza virus was determined to be the cause of death in 6 of 18 infected patients in Hong Kong. There was some evidence of human to human spreadA型流感病毒H3N2-M2蛋白抗体 of this virus, but it is thought that the transmission efficiency was fairly low. HA interacts with cell surface proteins containing oligosaccharides with terminal sialyl residues. Virus isolated from a human infected with the H5N1 strain in 1997 could bind to oligosaccharides from human as well as avian sources, indicating its species jumping ability.

A型流感病毒H3N2-M2蛋白抗体Also known as:

H3N2, matrix protein 2 [Influenza A virus (A/(A/Thailand/CU23/2006(H3N2))]; M2_I72A2; Matrix protein 2; Proton channel protein M2; M; [Influenza A virus (A/Udorn/307/1972(H3N2))].

Specificity:

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Rabbit Polyclonal IgG, affinity purified by Protein A.

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Reacts with: Influenza A virus H3N2.

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Immunogen: KLH conjugated synthetic peptide derived from human H3N2 Mat.

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A型流感病毒H3N2-M2蛋白抗体Predicted Molecular Weight: 11kDa.

Storage:

Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).

Application:

WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  ICC=1:100-500  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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