Eph receptor A4 antibody [N3C2-2], Internal detects Eph receptor A4 protein by western blot analysis. Whole cell extracts (30 μg) was separated by 5 % SDS-PAGE, and blotted with Eph receptor A4 antibody [N3C2-2], Internal (GTX111602) diluted by 1:1000

Mouse tissue extract (50 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with EphA4 antibody [N3C2], Internal (GTX111602) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various tissue extracts (50 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EphA4 antibody (GTX111602) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Sample (30 ug of whole cell lysate)
A: HeLa
7.5% SDS PAGE
GTX111602 diluted at 1:1000

Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with EphA4 antibody [N3C2-2], Internal (GTX111602) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.