DNase I, RNase-Free, HC Nuclease PCR and qPCR experiments

PCR and qPCR experiments

Unlike carboxyl or amino magnetic beads that require pre-activation with EDC/NHS or glutaraldehyde

Its fidelity is approximately 50 times higher than that of regular Taq DNA polymerase

and obtain a wider quantitative amplification region

The staining process is simple and fast

DNase I, RNase-Free, HC Nuclease PCR and qPCR experimentsConcentration: 50 U L Product Description DNase I (without RNase) is an endonuclease that can cleave both single stranded and double stranded DNA. It hydrolyzes phosphodiester bonds, producing single deoxyribonucleotides and oligodeoxyribonucleotides with 5' phosphate groups and 3' OH groups. The activity of this enzyme is strictly dependent on Ca2+ and is activated by Mg2+ or Mn2+ ions. In the presence of Mg2+, DNase I cuts each strand of dsDNA in a