Application
Various whole cell extracts (30 µg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Calnexin antibody diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Calnexin antibody [N3C2], Internal detects Calnexin protein at cytoplasm on mouse duodenum by immunohistochemical analysis. Sample: Paraffin-embedded mouse duodenum. Calnexin antibody [N3C2], Internal diluted at 1:500.
Application
Calnexin antibody [N3C2], Internal detects Calnexin protein at endoplasmic reticulum by immunofluorescent analysis. Sample: HeLa cells were fixed in ice-cold MeOH for 5 min. Green: Calnexin protein stained by Calnexin antibody [N3C2], Internal diluted at 1:200. Blue: Hoechst 33342 staining.
Application
Sample (30 µg of whole cell lysate) A: 293T B: A431 C: H1299 D: HeLa S3 E: HepG2 F: Molt-4 7.5% SDS PAGE diluted at 1:5000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Sample (30 µg of whole cell lysate) A:NIH-3T3 7.5% SDS PAGE diluted at 1:1000 The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Application
Immunohistochemical analysis of paraffin-embedded SAS xenograft, using Calnexin antibody at 1:100 dilution.
Application
Non-transfected (–) and transfected (+) 293T whole cell extracts (15 µg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with Calnexin antibody [N3C2], Internal diluted at 1:10000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.