DNA Polymerase I/DNase I is an optimized mixture of both enzymes for efficient nick translation of DNA.
Application:Labeling DNA with either radiolabeled or biotinylated nucleotides.
Source:DNase I is purified from bovine pancreas; DNA Polymerase I fromE. coli λlysogen NM 964.
Performance and Quality Testing:Performance tested in nick translation reaction.
Unit Definition:One unit of DNA Polymerase I in the absence of DNase I incorporates 10 nmol of total deoxyribonucleotide into acid-precipitable material in 30 min. at 37°C using a template•primer.
Unit Reaction Conditions:50 mM potassium phosphate (pH 7.5), 6.7 mM MgCl2, 1 mM 2-mercaptoethanol, 80 µg/ml template•primer, 32 µM dTTP, 69 nM [3H]dTTP, and enzyme in 100 µl for 30 min. at 37°C.
原厂资料:
DNA Polymerase I/DNase I is an optimized mixture of both enzymes for efficient nick translation of DNA.
Application:Labeling DNA with either radiolabeled or biotinylated nucleotides.
Source:DNase I is purified from bovine pancreas; DNA Polymerase I fromE. coli λlysogen NM 964.
Performance and Quality Testing:Performance tested in nick translation reaction.
Unit Definition:One unit of DNA Polymerase I in the absence of DNase I incorporates 10 nmol of total deoxyribonucleotide into acid-precipitable material in 30 min. at 37°C using a template•primer.
Unit Reaction Conditions:50 mM potassium phosphate (pH 7.5), 6.7 mM MgCl2, 1 mM 2-mercaptoethanol, 80 µg/ml template•primer, 32 µM dTTP, 69 nM [3H]dTTP, and enzyme in 100 µl for 30 min. at 37°C.
注意事项:
For Research Use Only. Not for use in diagnostic procedures.