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Purification of Epstein-Barr virus DNA polymerase from P3HR-1 cells.

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Figure

FIG.1.absenceextracts.butyrate-treatedrate-treatedcellsin the Induction of salt-stimulated DNA polymerase in n-buty- and untreated P3HR-1 cells
FIG. 2.polymerase DNA-cellulose chromatography of extracts from induced P3HR-1 cells. Fractions were assayed for nuclease activity (X) and DNA activity in the presence (A) and absence (A) of ammonium sulfate.
FIG. Phosphocelluloseose-purified 3. chromatography of the DNA-cellul( DNA polymerase
FIG. 6.acrylamideDNAwithBlue SDS-polyacrylamide gel electrophoresisin 12% poly- of (A) Blue Sepharose binding proteins eluted stepwise 0.4 to 1.0 M KCI (these fractions were not associated with any polymerase activity) and (B) EBV DNA polymerase from the Sepharose flow-through fraction.
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