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Protocol for Isolation of Genomic DNA from Mammalian Cells
(with RNase A, DNase and protease-free)

1. Trypsinize, harvest and resuspend cells at 10⁷/ ml in 10 mM Tris-HCl (pH 8.0), 10 mM EDTA.
2. Add SDS and Proteinase K to a final concentration of 0.5% and 200 µg/ml, respectively.
3. Mix and incubate at 55°C for 2 hours.
4. Add NaCl to a final concentration of 0.2M.
5. Extract twice with equal volumes of phenol:chloroform (1:1) and once with chloroform. Phenol must be equilibrated with buffer before use.
6. Place the tube, with cap open, in 55°C water bath for 1 hour, to evaporate the chloroform.
7. Add RNase A, DNase and protease-free to a final concentration of 25 µg/ml and incubate for 1 hour at 37°C. The concentration of the enzyme may vary for different cell types.
8. Extract once with phenol:chloroform (1:1) and once with chloroform. Precipitate DNA with 1.5 volumes of ethanol.
9. Centrifuge at 10000x g for 5 minutes to pellet the DNA.
10. Resuspend the pellet in 10 mM Tris-HCl (pH 8.0), 1 mM EDTA.

References

1. Sambrook, J., Russell, D.W., Molecular Cloning: A Laboratory Manual, the third edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, 1.31-1.38, 2001.
2. Sharma, R.C., et al., A rapid procedure for isolation of RNA-free genomic DNA from mammalian cells, BioTechniques, 14, 176-178, 1993.

Ordering Information

RNase A, DNase and protease-free RNase T1 RNase A/T1 Mix RNase I, E.coli Proteinase K GeneJET™ Plasmid Miniprep Kit Genomic DNA Purification Kit DEPC-teated Water Water, nuclease-free

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Updated sausio 31, 2008 15:18