Search
Search
View additional product information for dsDNase - FAQs (EN0771)
3 product FAQs found
No, dsDNase cleaves only double-stranded DNA. However, if ssDNA forms double-stranded structures, it will act as a target for dsDNase. Because of this, long and complex ssDNA may be partially degraded. Therefore we recommend additional dsDNase inactivation step for RT-PCR amplification of targets 3 kb or longer. The inactivation step should be performed by 5 min incubation at 55 degrees C in the presence of 10 mM DTT.
No. RT reaction composition inhibits dsDNase activity, and genomic DNA removal may be incomplete.
Yes. dsDNase buffer is not needed for subsequent reverse transcription reaction. If RNA sample is not contaminated with gDNA, dsDNase treatment may be omitted.