Western blotting analysis using SSR1 antibody (Cat#6590). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SSR1 antibody (Cat#6590, 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 SSR1 antibody (Cat#6590, 1:1,000). Nuclei were stained blue with DAPI; SSR1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. 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 SSR1 expression in HepG2 cells using SSR1 antibody (Cat#6590, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, SSR1.
SSR1; Signal Sequence Receptor Subunit 1; TRAPA; Translocon-Associated Protein Subunit Alpha; Signal Sequence Receptor Subunit Alpha; Signal Sequence Receptor, Alpha; SSR-Alpha; Translocon-Associated Protein Alpha Subunit; Translocon-Associated Protein Alpha; SSR Alpha Subunit; TRAP Alpha; TRAP-Alpha
Western blotting analysis using SSR1 antibody (Cat#6590). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SSR1 antibody (Cat#6590, 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 SSR1 antibody (Cat#6590, 1:1,000). Nuclei were stained blue with DAPI; SSR1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. 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 SSR1 expression in HepG2 cells using SSR1 antibody (Cat#6590, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, SSR1.
Western blotting analysis using SSR1 antibody (Cat#6590). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with SSR1 antibody (Cat#6590, 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 SSR1 antibody (Cat#6590, 1:1,000). Nuclei were stained blue with DAPI; SSR1 was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Low. 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 SSR1 expression in HepG2 cells using SSR1 antibody (Cat#6590, 1:2,000). Fixative solution: 4% Paraformaldehyde in 1x PBS; Permeabilization solution: 100% Methanol, chill on -20℃ before use. Green, isotype control; red, SSR1.
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