A型禽流感病毒H1N1蛋白抗体

Quantity size:

0.2ml

Concentration:

1mg/ml A型禽流感病毒H1N1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; 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 A型禽流感病毒H1N1蛋白抗体(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 spread of this virus, but it is thought that the transmission efficiency was fairly low. HA interacts with cell surface proteins containing oligosaccharides A型禽流感病毒H1N1蛋白抗体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.

Also known as:

Influenza A virus (A/California/04/2009(H1N1))Matrix Protein-1; H1N1 M1.

Specificity:

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Rabbit Polyclonal IgG,A型禽流感病毒H1N1蛋白抗体 affinity purified by Protein A.

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Reacts with: Influenza A virus H1N1.

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Immunogen: KLH conjugated synthetic peptide derived from H1N1 Matrix Pr.

A型禽流感病毒H1N1蛋白抗体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  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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