Flow cytometric analysis of GC1q R expression in HepG2 cells using GC1q R antibody (Cat#69616, 1:2,000). Green, isotype control; red, GC1q R.
Immunocytochemical staining of HepG2 cells with GC1q R antibody (Cat#69616, 1:1,000). Nuclei were stained blue with DAPI; GC1q R 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-GC1q R antibody (Cat#69616). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-GC1q R antibody (Cat#69616, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-GC1q R antibody (Cat#69616). GC1q R expression in wild type (WT) and GC1q R 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-GC1q R antibody (Cat#69616, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:50,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Validation of GC1qR knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with anti-GC1qR antibody (Cat#69616, 1:2,000) and analyzed using BD flow cytometer.
