Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Venezuelan Equine Encephalitis Virus nsP2 antibody [HL1919] (GTX637668) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Venezuelan Equine Encephalitis Virus nsP2 antibody [HL1919] (GTX637668) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.

Immunofluorescent analysis of Venezuelan equine encephalitis virus infected cells using Venezuelan Equine Encephalitis Virus nsP2 antibody [HL1919] (GTX637668).
Sample: Multiple virus infected cells slide.
Green: Venezuelan Equine Encephalitis Virus nsP2 antibody [HL1919] (GTX637668) diluted at 1:100.
Blue: Fluoroshield with DAPI (GTX30920).