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Isolation of High‐Molecular‐Weight DNA from Mammalian Cells

European Journal of Biochemistry · 1973 · Vol. 36(1) · pp. 32–38
M. Gross-BellardP OudetPierre Chambon

Abstract

A preparative method for isolating high‐molecular‐weight DNA from animal cells is described. This method is based on the use of proteinase K, a powerful proteolytic enzyme with a broad action spectrum, which is very active in the presence of sodium dodecylsulfate and ethylene‐diamine tetraacetate. The DNA preparation is free of RNA, protein and degrading enzymes. The number‐average molecular weight of the native DNA is 190 × 10 6 , whereas it is 90 × 10 6 for single‐stranded DNA, indicating that the DNA molecules do not contain single‐stranded nicks. The native DNA molecules range in molecular weight from 40 × 10 6 to more than 500 × 10 6 .

MeSH terms

AnimalsHaplorhiniCell FractionationCell LineCentrifugation, Density GradientDNADNA, Single-StrandedEdetic AcidKidneyMacacaMethodsMicroscopy, ElectronMolecular WeightNucleotidyltransferasesPeptide Hydrolases
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References
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Journal of Biological Chemistry · 1951 · 317,666 citations
Sedimentation studies of the size and shape of DNA
Journal of Molecular Biology · 1965 · 2,169 citations
A procedure for the isolation of deoxyribonucleic acid from micro-organisms
Journal of Molecular Biology · 1961 · 11,579 citations
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