Get tips on using E-Gel™ Ultra Low Range DNA Ladder to perform DNA Ladder Low Range
Get tips on using E-Gel™ Low Range Quantitative DNA Ladder to perform DNA Ladder Low Range
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Get tips on using Quick-Load® Purple 1 kb DNA Ladder to perform DNA Ladder 1 kb
Get tips on using Quick-Load® 1 kb Extend DNA Ladder to perform DNA Ladder 1 kb
Get tips on using Quick-Load® 1 kb Plus DNA Ladder to perform DNA Ladder 1 kb
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Get tips on using E-Gel™ 1 Kb Plus DNA Ladder to perform DNA Ladder 1 kb
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I am currently using a recombinant protein which shows metal-dependent DNase activity. Is it possible to pinpoint the source of the DNase activity after protein purification? More specifically, can I ensure that the DNase activity is not because of nuclease contamination from the E.coli that might have persisted and passed with the protein of interest during purification?
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