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. 2009 Mar 25;8(7):1579–1598. doi: 10.1074/mcp.M800601-MCP200

Table I. Biochemical analysis of nuclear purity.

Nuclear purity was determined on the basis of marker enzyme activities specific for cytosol (alcohol dehydrogenase), microbody (catalase), mitochondria (fumarase hydratase), and plastid (glucose-6-phosphate dehydrogenase). Experiments were done in triplicates. CE, crude extract; N1, nuclear fraction without wash; N2, nuclear fraction after first wash; N, final purified nuclear fraction.

Fraction Catalase
Alcohol dehydrogenase
Glucose-6-phosphate dehydrogenase
Fumarate hydratase
Activity % of CE Activity % of CE Activity % of CE Activity % of CE
μmol/mg/min μmol/mg/min μmol/mg/min μmol/mg/min
Crude extract 28.02 ± 0.58 100 3140 × 10−5 ± 0.00004 100 158 × 10−4 ± 0.00018 100 6920 × 10−3 ± 0.17 100
N1 5.01 ± 0.025 17.88 470 × 10−5 ± 0.00002 14.96 25.9 × 10−4 ± 0.00015 16.39 1090 × 10−3 ± 0.020 15.75
N2 1.08 ± 0.011 3.85 70 × 10−5 ± 0.00001 2.22 4.5 × 10−3 ± 0.00012 2.848 172.50 × 10−3 ± 0.0018 2.49
N 0.035 ± 0.004 0.12 3.3 × 10−5 ± 0.00003 0.1 0.36 × 10−4 ± 0.00014 0.22 12.58 × 10−3 ± 0.0019 0.18