Western blot analysis of extracts of THP-1 cells, using Anti-CD34 Antibody (A15690) 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.
Western blot analysis of extracts from normal (control) and CD34 Rabbit polyclonal antibody knockout (KO) 293T cells, using Anti-CD34 Antibody (A15690) at 1:3,000 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.
Immunofluorescence analysis of TF-1 cells using Anti-CD34 Antibody (A15690) at a dilution of 1:200 (40x lens). DAPI was used to stain the cell nuclei (blue).
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