CYP26B1抗体 [N2C2], Internal

Whole cell extract (30 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with CYP26B1 antibody [N2C2], Internal (GTX104932) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Whole cell extract (30 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with CYP26B1 antibody [N2C2], Internal (GTX104932) 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 CYP26B1 antibody [N2C2], Internal (GTX104932) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Immunohistochemical analysis of agarose-embedded zebrafish embryo cross-section, using CYP26B1 antibody [N2C2], Internal (GTX104932) at 1:200 dilution.