West Nile virus Capsid protein antibody

Non-infected (–) and infected (+) Huh-7 whole cell extracts (5 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with West Nile virus Capsid protein antibody (GTX131947) 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 Vero whole cell extracts were separated by SDS-PAGE, and the membrane was blotted with West Nile virus Capsid protein C antibody (GTX131947).

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with West Nile virus Capsid protein C antibody (GTX131947) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.