Skip to main content
. 2010 Jun 16;73(8):1612–1631. doi: 10.1016/j.jprot.2010.03.018

Table 6.

Proteins regulated by Nrf2 identified by 2DE analysis.

Protein spot SwissProt acc. No. Protein Mr/pI Normalized spot Intensity (% total spot intensity)
Fold change
p
Nrf2(+/+) Nrf2(−/−) (Nrf2(−/−)/ Nrf2(+/+))
1 P24549 Aldehyde dehydrogenase family 1, subfamily A1 54468/7.91 0.19 ± 0.01 0.15 ± 0.01 0.78 0.0025
2 P10649 Glutathione S-transferase, mu 1 25970/7.7 0.88 ± 0.20 0.53 ± 0.07 0.60 0.0158
3 P30115 Glutathione S-transferase, alpha 3 25361/8.76 0.85 ± 0.09 0.67 ± 0.02 0.80 0.0098
4a P19157 Glutathione S-transferase, pi 1 23609/7.69 2.06 ± 0.17 1.20 ± .50 0.58 0.0170
4b P19157 Glutathione S-transferase, pi 1 23609/7.69 0.29 ± 0.03 0.017 ± 0.05 0.57 0.0040
4c P19157 Glutathione S-transferase, pi 1 23609/7.69 0.21 ± 0.01 0.11 ± 0.05 0.50 0.0073
5 Q923D2 Biliverdin reductase B 22197/6.49 0.13 ± 0.01 0.010 ± 0.01 0.83 0.0155
6 P11588 Major urinary protein 6 20648/5.0 0.46 ± 0.06 0.17 ± 0.05 0.36 0.0002

Proteins from the livers of individual mice were separated by 2-DE as described in the Materials and methods. The protein spots were quantified from colloidal Coomassie blue-stained gels using ImageMasterTM 2D Elite software. Spot intensities were normalized to the total spot intensity for each gel and expressed as the mean percentage value ± SD (n = 4 for each group). Proteins that were significantly different (Student's t-test; p < 0.05) between the wild type and Nrf2 null mice are shown.