Western Blot - Anti-Glucose Transporter GLUT4 Antibody (A15818)
Western blot analysis of extracts of various cell lines, using Anti-Glucose Transporter GLUT4 Antibody (A15818) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 30s.
Western Blot - Anti-Glucose Transporter GLUT4 Antibody (A15818)
Western blot analysis of extracts of various cell lines, using Anti-Glucose Transporter GLUT4 Antibody (A15818) at 1:1,000 dilution. The secondary antibody was Goat Anti-Rabbit IgG H&L Antibody (HRP) at 1:10,000 dilution. Lysates/proteins were present at 25µg per lane. The blocking buffer used was 3% non-fat dry milk in TBST. Detection was with a ECL Basic Kit. Exposure time: 90s.
Immunohistochemistry analysis of paraffin-embedded mouse skeletal muscle using Anti-Glucose Transporter GLUT4 Antibody (A15818) at a dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunohistochemistry analysis of paraffin-embedded mouse skeletal muscle using Anti-Glucose Transporter GLUT4 Antibody (A15818) at a dilution of 1:100 (40x lens). Perform microwave antigen retrieval with 10 mM Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
Immunofluorescence analysis of mouse skeletal muscle using Anti-Glucose Transporter GLUT4 Antibody (A15818) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of RD cells using Anti-Glucose Transporter GLUT4 Antibody (A15818) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of C2C12 cells using Anti-Glucose Transporter GLUT4 Antibody (A15818) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).
