- Prepare the following reaction mixture:
Digested DNA (aqueous solution) 10-15 µl (0.1-4 µg) 10X reaction buffer for Klenow Fragment 2 µl dNTP Mix, 2 mM each 0.5 µl (0.05 mM final concentration) Klenow fragment 0.1-0.5 µl (1-5 u) Water, nuclease-free to 20 µl - Incubate the mixture at 37°C for 10 minutes.
- Stop the reaction by heating at 75°C for 10 minutes.
Reference
Ausubel, F.M., et al., Current Protocols in Molecular Biology, vol. 1, John Wiley & Sons, Inc., Brooklyn, New York, 3.5.7-3.5.10, 1994-2005.
Ordering Information
- Klenow Fragment
- dNTP Mixes
- dNTP Set
- Modified Nucleotides (molecular biology grade):
Aminoallyl-dUTP
Biotin-11-dUTP
Fluorescein-12-dUTP
dm6ATP
dm4CTP
dm5CTP- M-MuLV Reverse Transcriptase
- RevertAid™ M-MuLV Reverse Transcriptase
- RevertAid™ H Minus M-MuLV Reverse Transcriptase
- RNase H, E.coli
- Pyrophosphatase, Inorganic (from yeast)
- 0.5 M EDTA, pH 8.0
- Water, nuclease-free
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Updated sausio 31, 2008 15:19