Western blotting analysis using AKT1 antibody (Cat#4150). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with AKT1 antibody (Cat#4150, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunohistochemistry was performed on paraffin-embedded human ovarian carcinoma using AKT1 antibody (Cat#4150, 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.
Immunocytochemical staining of C2C12 cells with AKT1 antibody (Cat#4150, 1:1,000). Nuclei were stained blue with DAPI; AKT1 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.
Flow cytometric analysis of AKT1 expression in C2C12 cells using AKT1 antibody (Cat#4150, 1:2,000). Green, isotype control; red, AKT1.
Western blotting analysis using AKT1 antibody (Cat#4150). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with AKT1 antibody (Cat#4150, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunohistochemistry was performed on paraffin-embedded human ovarian carcinoma using AKT1 antibody (Cat#4150, 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.
Immunocytochemical staining of C2C12 cells with AKT1 antibody (Cat#4150, 1:1,000). Nuclei were stained blue with DAPI; AKT1 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.
Flow cytometric analysis of AKT1 expression in C2C12 cells using AKT1 antibody (Cat#4150, 1:2,000). Green, isotype control; red, AKT1.
Western blotting analysis using AKT1 antibody (Cat#4150). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with AKT1 antibody (Cat#4150, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunohistochemistry was performed on paraffin-embedded human ovarian carcinoma using AKT1 antibody (Cat#4150, 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.
Immunocytochemical staining of C2C12 cells with AKT1 antibody (Cat#4150, 1:1,000). Nuclei were stained blue with DAPI; AKT1 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.
Flow cytometric analysis of AKT1 expression in C2C12 cells using AKT1 antibody (Cat#4150, 1:2,000). Green, isotype control; red, AKT1.
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