Western blot analysis of extracts of various cell lines, using Anti-Factor H Antibody (A9001) 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.
Western blot analysis of extracts of Rat liver, using Anti-Factor H Antibody (A9001) 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 analysis of extracts of Human plasma, using Anti-Factor H Antibody (A9001) 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.
Immunohistochemistry - Anti-Factor H Antibody (A9001)
Immunohistochemistry analysis of paraffin-embedded human placenta using Anti-Factor H Antibody (A9001) at a dilution of 1:100 (40x lens). Perform high pressure antigen retrieval with 10 mM citrate buffer pH 6.0 before commencing with IHC staining protocol.
Immunofluorescence - Anti-Factor H Antibody (A9001)
Immunofluorescence analysis of HepG2 cells using Anti-Factor H Antibody (A9001) at a dilution of 1:100 (40x lens). DAPI was used to stain the cell nuclei (blue).