Formalin-fixed and paraffin-embedded human hepatocarcinoma tissue reacted with GAPDH antibody , which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.
GAPDH Antibody confocal immunofluorescent analysis with HeLa cell. 0.025 mg/ml primary antibody was followed by FITC-conjugated goat anti-rabbit lgG (whole molecule). FITC emits green fluorescence. DAPI was used to stain the cell nuclear (blue).
Confocal immunofluorescent of GAPDH Antibody with HeLa cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green). Actin filaments have been labeled with Alexa Fluor 555 phalloidin (red). DAPI was used to stain the cell nuclear (blue).
Western blot of lysates from HeLa,HUVEC cell line (from left to right),using GAPDH Antibody. Antibody was diluted at 1:1000 at each lane. A goat anti-rabbit IgG H&L (HRP) at 1:5000 dilution was used as the secondary antibody.Lysates at 35ug per lane.
Western blot of GAPDH Antibody in A2058, A375, CEM cell line lysates (35 ug/lane). GAPDH (arrow) was detected using the purified antibody.