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Flow cytometric analysis of MAP2K3 expression in C2C12 cells using MAP2K3 antibody. Green, isotype control; red, MAP2K3.
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Immunocytochemical staining of C2C12 cells with MAP2K3 antibody. Nuclei were stained blue with DAPI; MAP2K3 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.
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Immunohistochemistry was performed on paraffin-embedded human lung adenocarcinoma using MAP2K3 antibody. 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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Immunohistochemistry was performed on paraffin-embedded mouse liver using MAP2K3 antibody. 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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Immunohistochemistry was performed on paraffin-embedded mouse spleen using MAP2K3 antibody. 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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Immunohistochemistry was performed on paraffin-embedded mouse kidney using MAP2K3 antibody. 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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Western blotting analysis using MAP2K3 antibody. Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with MAP2K3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively.