Influenza B virus M (matrix protein)抗体 [HL5332]

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Influenza B virus M (matrix protein) antibody [HL5332] (GTX645810) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Non-infected (–) and infected (+) MDCK whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Influenza B virus M (matrix protein) antibody [HL5332] (GTX645810) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate.