RNase-Free DNase I, 5,000 U @ 1 U/uL size:EACH If used with 1

If used with 1

PCR amplicons from the 3´ end and 5´ end of the GUSB cDNA

catalyzes degradation of ssDNA in a 5´ to 3´ direction

CircLigase II has greater activity and a new Reaction Buffer for improved ligation efficiency

and all other samples with QuickExtract™ DNA Extraction Solution

RNase-Free DNase I, 5,000 U @ 1 U/uL size:EACH If used with 1Degrade dsDNA and ssDNA without damaging important RNA in your sample or reaction Digest away unwanted DNA without digesting RNA Use in a variety of applications such as in vitro transcription and RT PCR Applications Elimination of template DNA following in vitro synthesis of RNA with T7, SP6, or T3 RNA polymerase. Labeling of DNA by nick translation, in combination with Klenow or other DNA polymerases. Treatment of RNA prior to RT PCR. 1