Western blotting analysis using SNRPB antibody (Cat#5288). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SNRPB antibody (Cat#5288, 1:2,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with SNRPB antibody (Cat#5288, 1:1,000). Nuclei were stained blue with DAPI; SNRPB was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of SNRPB expression in HepG2 cells using SNRPB antibody (Cat#5288, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, SNRPB.
SNRPB; Small Nuclear Ribonucleoprotein Polypeptides B And B1; Sm-B/B'; SnRNP-B; COD; SmB/SmB'; SNRPB1; Small Nuclear Ribonucleoprotein-Associated Proteins B And B'; Sm Protein B/B'; SmB/B'; Small Nuclear Ribonucleoprotein Polypeptides B And B'; Small Nuclear Ribonucleoprotein Polypeptide B; B Polypeptide Of Sm Protein; Sm-B/Sm-B'; CCMS
Western blotting analysis using SNRPB antibody (Cat#5288). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SNRPB antibody (Cat#5288, 1:2,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with SNRPB antibody (Cat#5288, 1:1,000). Nuclei were stained blue with DAPI; SNRPB was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of SNRPB expression in HepG2 cells using SNRPB antibody (Cat#5288, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, SNRPB.
Western blotting analysis using SNRPB antibody (Cat#5288). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SNRPB antibody (Cat#5288, 1:2,000) and HRP-conjugated goat anti-mouse secondary antibody (Cat#101, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Immunocytochemical staining of HepG2 cells with SNRPB antibody (Cat#5288, 1:1,000). Nuclei were stained blue with DAPI; SNRPB was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Scale bar: 20 μm.
Flow cytometric analysis of SNRPB expression in HepG2 cells using SNRPB antibody (Cat#5288, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 0.5% Triton X-100 in 1x PBS. Green, isotype control; red, SNRPB.
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