Figures & data
Table 1. Summary of the analytical parameters.
Figure 1. Typical heart tissue chromatograms of (a) carbonyl proteins in guanidine detected after reaction with 2,4-dinitrophenylhydrazine at 370 nm and (b) malondialdehyde in butanol detected after reaction with thiobarbituric acid at 532 nm including blanks (gray lines). The mobile phase was pH 6.9 100 mM ammonium acetate buffer and acetonitrile (1 + 1). The stationary phase was a reverse phase C18 column.
![Figure 1. Typical heart tissue chromatograms of (a) carbonyl proteins in guanidine detected after reaction with 2,4-dinitrophenylhydrazine at 370 nm and (b) malondialdehyde in butanol detected after reaction with thiobarbituric acid at 532 nm including blanks (gray lines). The mobile phase was pH 6.9 100 mM ammonium acetate buffer and acetonitrile (1 + 1). The stationary phase was a reverse phase C18 column.](/cms/asset/77ae1bf2-a4e1-45cc-8865-0bafd6e187ab/lanl_a_1505899_f0001_b.jpg)