Respiratory Syncytial virus type A G protein抗体 [HL3122]

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Respiratory Syncytial virus type A G protein antibody [HL3122] (GTX640598) 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.

Non-infected (–) and infected (+) HEp-2 whole cell extracts (5 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Respiratory Syncytial virus type A G protein antibody [HL3122] (GTX640598) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.