Western blotting analysis using β-Actin antibody (Cat#3784). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with β-Actin antibody (Cat#3784, 1:10,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 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 β-Actin antibody (Cat#3784, 1:2,000). Green, isotype control; red, β-Actin.
Immunocytochemical staining of HepG2 cells with β-Actin protein antibody (Cat#3784, 1:1,000). Nuclei were stained blue with DAPI; β-Actin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Scale bar, 20 μm. Permeabilization: Triton.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using β-actin antibody (Cat#3784, 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 β-Actin antibody (Cat#3784). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with β-Actin antibody (Cat#3784, 1:10,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 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 β-Actin antibody (Cat#3784, 1:2,000). Green, isotype control; red, β-Actin.
Immunocytochemical staining of HepG2 cells with β-Actin protein antibody (Cat#3784, 1:1,000). Nuclei were stained blue with DAPI; β-Actin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Scale bar, 20 μm. Permeabilization: Triton.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using β-actin antibody (Cat#3784, 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 β-Actin antibody (Cat#3784). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with β-Actin antibody (Cat#3784, 1:10,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 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 β-Actin antibody (Cat#3784, 1:2,000). Green, isotype control; red, β-Actin.
Immunocytochemical staining of HepG2 cells with β-Actin protein antibody (Cat#3784, 1:1,000). Nuclei were stained blue with DAPI; β-Actin was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. Scale bar, 20 μm. Permeabilization: Triton.
Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using β-actin antibody (Cat#3784, 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.
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