Flow cytometric analysis of β-Actin expression in HepG2 cells using anti-β-Actin antibody (Cat#3786, 1:2,000). Green, isotype control; red, β-Actin.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using anti-β-actin antibody (Cat#3786, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Western blotting analysis using anti-β-Actin antibody (Cat#3786). Total cell lysates (20 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-β-Actin antibody (Cat#3786, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of β-Actin expression in HepG2 cells using anti-β-Actin antibody (Cat#3786, 1:2,000). Green, isotype control; red, β-Actin.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using anti-β-actin antibody (Cat#3786, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Western blotting analysis using anti-β-Actin antibody (Cat#3786). Total cell lysates (20 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-β-Actin antibody (Cat#3786, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of β-Actin expression in HepG2 cells using anti-β-Actin antibody (Cat#3786, 1:2,000). Green, isotype control; red, β-Actin.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using anti-β-actin antibody (Cat#3786, 1:200). Antigen retrieval was done in sodium citrate buffer (pH 6.0). DAB was used for detection, with hematoxylin counterstaining. Images were acquired using a Nikon Ci-L Plus microscope (40× objective). Scale bar: 25 μm.
Western blotting analysis using anti-β-Actin antibody (Cat#3786). Total cell lysates (20 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-β-Actin antibody (Cat#3786, 1:50,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
