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eliminating the requirement to remove the enzyme prior to many subsequent procedures
virtually no linear concatamers or circular concatamers are produced
PCR amplicons from the 3´ end and 5´ end of the GUSB cDNA
One µl of Ready-Lyse Solution was added to each suspension and the cells were incubated at room temperature for 30 minutes
In ClearColi
RNase-Free DNase I, 5,000 U @ 1 U/uL size:EACH eliminating the requirement to removeDegrade 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
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