Exonuclease VII, 250 U @ 10 U/uL ISOBUC Improved success in demanding downstream

Improved success in demanding downstream applications

Preserves Yields

No detectable DNA contamination as determined by PCR using generic primers

Addition of a poly(A) tail to an RNA molecule or a mixture of RNA molecules in order to provide a priming site for synthesis of first-strand cDNA using a primer with poly(dT) on its 3´ end

HI-Control™ BL21(DE3) and HI-Control™ 10G Competent Cells

Exonuclease VII, 250 U @ 10 U/uL ISOBUC Improved success in demanding downstreamDigest duplex DNA in a 3 to 5 direction from a nick, blunt end, or 3 recessed end, producing stretches of ssDNA. Produce stretches of ssDNA in dsDNA templates containing nicks, blunt ends or recessed 3' ends Protect protruding 3' ends becuase this exonuclease will not start digestion at protruding 3' overhangs Applications Production of intermediates for site directed mutagenesis. 1 3 Production of strand specific radiolabeled probes. 4 Exonuclease