Figure 1: Western Blot - Anti-Heme Oxygenase 1 Antibody (A307279)
Western blot analysis of extracts of HeLa cells, using Anti-Heme Oxygenase 1 Antibody (A307279) 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: 10s.
Figure 2: Western Blot - Anti-Heme Oxygenase 1 Antibody (A307279)
Western blot analysis of extracts of various cell lines, using Anti-Heme Oxygenase 1 Antibody (A307279) 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.
Figure 3: Western Blot - Anti-Heme Oxygenase 1 Antibody (A307279)
Western blot analysis of extracts of HepG2 cells, using Anti-Heme Oxygenase 1 Antibody (A307279) 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: 180s.
Immunofluorescence analysis of PC-12 using Anti-Heme Oxygenase 1 Antibody (A307279) at dilution of 1 : 50 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of HepG2 using Anti-Heme Oxygenase 1 Antibody (A307279) at dilution of 1 : 50 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of NIH-3T3 using Anti-Heme Oxygenase 1 Antibody (A307279) at dilution of 1 : 50 (40x lens). DAPI was used to stain the cell nuclei (blue).
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