J. Cao et al., Supp. Figure 1

5 downloads 0 Views 8MB Size Report
C51/172S/H-Ras. Prdx1+/+. Prdx1-/-. 25. 20. 15. 10. 5. 0. H. 2. O. 2. (n m o l)/1. 0. ^. 6 c e lls. 50. 150. 100. 200. 0. 250. Time (min). Prdx1-/- Prdx1C51/172S.
A H2O2(nmol)/10^6 cells

25

** *

Prdx1-/- Prdx1C51/172S Prdx1-/-

20

** *

15

Prdx1-/-WT

** *

*

10

5

*

0 0

50

B

100 150 Time (min)

200

250

H2O2 release of Prdx1-/-MEFs (filled square), Prdx1-/-MEFs reconstituted with the Prdx1 wildtype gene (Prdx1WT) (filled triangle) and Prdx1-/-MEFs expressing Prdx1C51/172S (filled circle) were measured as described in detail in Materials and methods, by using Amplex Red reagent, which via oxidation, becomes fluorescent resorufin. The y-Axis presents H2O2 release accumulated over time per 1x10^6 cells. For each clone, 6 wells were plated and analyzed. The experiment shown here is representative of 5 independent studies from 3 different sets of MEF clones from Prdx1-littermates. P values were calculated using an unpaired Student's t-Test. *P