FIELD: medicine.
SUBSTANCE: method includes alkaline lysis of bacterial cells and depositing of cellular walls by centrifugation. Afterwards supernatant is filtered, and RNA admixture is removed from produced filtrate by means of filtrate treatment with RNA-ase. Then plasmid DNA is deposited with isopropyl alcohol. Then divisional fractioning of plasmid DNA is carried out with ethyl alcohol, when first ethyl alcohol is added to solution of plasmid DNA to concentration of 45-53%, then ethyl alcohol is added to concentration of 55-58%, and in the end ethyl alcohol is added to concentration of 60-67%. Afterwards lipopolysaccharide remains are removed with the help of reverse-phase sorbent with hydrophobised surface.
EFFECT: improved cleanliness and yield of plasmid DNA.
3 cl, 1 tbl, 4 ex
Authors
Dates
2011-01-10—Published
2009-04-06—Filed