Figure 1: Western Blot - Anti-Cytochrome C Antibody (A12553)
Western blot analysis of extracts from normal (control) and Cytochrome C knockout (KO) 293T cells, using Anti-Cytochrome C Antibody (A12553) 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: 1s.
Figure 2: Western Blot - Anti-Cytochrome C Antibody (A12553)
Western blot analysis of extracts of various cell lines, using Anti-Cytochrome C Antibody (A12553) 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: 1s.
Figure 3: Immunohistochemistry - Anti-Cytochrome C Antibody (A12553)
Immunohistochemistry analysis of paraffin-embedded human breast cancer tissue using Anti-Cytochrome C Antibody (A12553) 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.
Figure 4: Immunohistochemistry - Anti-Cytochrome C Antibody (A12553)
Immunohistochemistry analysis of paraffin-embedded human oophoroma using Anti-Cytochrome C Antibody (A12553) 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.
Figure 5: Immunofluorescence - Anti-Cytochrome C Antibody (A12553)
Immunofluorescence analysis of NIH/3T3 cells using Anti-Cytochrome C Antibody (A12553) at a dilution of 1:200 (40x lens). DAPI was used to stain the cell nuclei (blue).
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