Western blot analysis of various lysates, using Anti-XBP1 Antibody (A309876) at 1:400 dilution. HeLa, C2C12 and cells were treated by TSA (1 uM) at 37°C for 18 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: 20s.
Western blot analysis of Rat lung, using Anti-XBP1 Antibody (A309876) at 1:400 dilution. HeLa, C2C12 and cells were treated by TSA (1 uM) at 37°C for 18 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 Enhanced Kit (RM00021). Exposure time: 60s.
Immunofluorescence analysis of Hep-G2 cells using Anti-XBP1 Antibody (A309876) at a dilution of 1:20 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of HT-29 cells using Anti-XBP1 Antibody (A309876) at a dilution of 1:20 (40x lens). DAPI was used to stain the cell nuclei (blue).
Immunofluorescence analysis of NIH/3T3 cells using Anti-XBP1 Antibody (A309876) at a dilution of 1:20 (40x lens). DAPI was used to stain the cell nuclei (blue).