Flow cytometric analysis of Growth associated protein 43 expression in HAP-1 cells using Growth associated protein 43 antibody (Cat#63163, 1:2,000). Green, isotype control; red, Growth associated protein 43.
Immunocytochemical staining of HAP-1 cells with Growth associated protein 43 antibody (Cat#63163, 1:1,000). Nuclei were stained blue with DAPI; Growth associated protein 43 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar: 20 μm.
Western blotting analysis using anti-Growth associated protein 43 antibody (Cat#63163). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-Growth associated protein 43 antibody (Cat#63163). Growth associated protein 43 expression in wild type (WT) and growth associated protein 43 shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. β-Tubulin serves as a loading control. The blot was incubated with anti-Growth associated protein 43 antibody (Cat#63163, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Validation of Growth associated protein 43 knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-Growth associated protein 43 antibody (Cat#63163, 1:2,000) and analyzed using CytoFLEX.
Immunocytochemical staining of HeLa cells using anti-GAP43 antibody (Cat#63163, 1:1,000), Top panel: wild-type (WT); Bottom panal: GAP43 shRNA knockdown (KD). Nuclei were stained blue with DAPI; GAP43 was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.
