|
Figure 3
Absorption spectra of purified AtGSA1. The enzyme was at different concentrations (0.8, 1.6 and 4 mg ml−1) in buffer consisting of 20 mM Tris–HCl pH 7.5, 200 mM NaCl. The buffer was used as a control. |
|
Figure 3
Absorption spectra of purified AtGSA1. The enzyme was at different concentrations (0.8, 1.6 and 4 mg ml−1) in buffer consisting of 20 mM Tris–HCl pH 7.5, 200 mM NaCl. The buffer was used as a control. |