Application
Non-transfected (–) and transfected (+) HepG2 whole cell extracts (30 µg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Grp78 antibody [N2C1], Internal diluted at 1:200. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Grp78 antibody [N2C1], Internal detects Grp78 protein at endoplasmic reticulum by immunofluorescent analysis. Sample: HeLa cells were fixed in ice-cold MeOH for 5 min. Green: Grp78 protein stained by Grp78 antibody [N2C1], Internal diluted at 1:100. Blue: Hoechst 33342 staining.
Application
Immunoprecipitation of Grp78 protein from HepG2 whole cell extracts using 5 μg of Grp78 antibody [N2C1], Internal . Western blot analysis was performed using Grp78 antibody [N2C1], Internal . EasyBlot anti-Rabbit IgG was used as a secondary reagent.
Application
Grp78 antibody [N2C1], Internal detects Grp78 protein at cytosol on mouse intestine by immunohistochemical analysis. Sample: Paraffin-embedded mouse intestine. Grp78 antibody [N2C1], Internal dilution: 1:50.
Application
Grp78 antibody [N2C1], Internal detects Grp78 protein at cytosol on rat hind brain by immunohistochemical analysis. Sample: Paraffin-embedded rat hind brain. Grp78 antibody [N2C1], Internal dilution: 1:50.
Application
Grp78 antibody [N2C1], Internal detects Grp78 protein at cytoplasm in mouse brain by immunohistochemical analysis. Sample: Paraffin-embedded mouse brain. Grp78 antibody [N2C1], Internal diluted at 1:50.
Application
Grp78 antibody [N2C1], Internal detects Grp78 protein at cytoplasm in rat prostate by immunohistochemical analysis. Sample: Paraffin-embedded rat prostate. Grp78 antibody [N2C1], Internal diluted at 1:50.
Application
Grp78 antibody detects Grp78 protein by western blot analysis. Various whole cell extracts (30 µg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Grp78 antibody diluted at a dilution of 1:200. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.