RNase-Free DNase I, 10,000 U @ 1 U/uL size:EACH Easy to handle and quick

Easy to handle and quick to use

making it easier to remove the resulting lipid IVA from the downstream product

Cells containing a T7 expression plasmid harboring a gene encoding the human apolipoprotein A1 (ApoA1) were grown in LB Miller medium at 37°C

5´ pN—OH 3´ + Pi

The device is fully specified for sample transport and storage

RNase-Free DNase I, 10,000 U @ 1 U/uL size:EACH Easy to handle and quickDegrade 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