Figure 1: Western Blot - Anti-Vimentin (phospho Ser83) Antibody (A308301)
Western blot analysis of extracts of NIH/3T3 cells, using Anti-Vimentin (phospho Ser83) Antibody (A308301) at 1:1,000 dilution. NIH/3T3 cells were treated by Paclitaxel (100 nM/ml) at 37°C for 20 hours. NIH/3T3 cells were treated by Hydroxyurea (4 mM) at 37°C for 20 hours. 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-Vimentin (phospho Ser83) Antibody (A308301)
Western blot analysis of extracts of C6 cells, using Anti-Vimentin (phospho Ser83) Antibody (A308301) at 1:1,000 dilution. C6 cells were treated by Paclitaxel (100 nM) at 37°C for 20 hours. 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 3: Western Blot - Anti-Vimentin (phospho Ser83) Antibody (A308301)
Western blot analysis of extracts of HeLa cells, using Anti-Vimentin (phospho Ser83) Antibody (A308301) at 1:1,000 dilution. HeLa cells were treated by Paclitaxel (100 nM/ml) at 37°C for 20 hours. HeLa cells were treated by Hydroxyurea (4 mM) at 37°C for 20 hours. 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.
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