DNA/RNA modifying enzymes

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An advanced enzyme developed through in vitro evolution of M-MuLV RT.

A genetically modified M-MuLV RT for routine performance in reverse transcription.

Uracil-DNA glykosyláza (UDG, UNG) katalyzuje hydrolýzu N-glykosylové vazby mezi uracilem a cukrem v DNA a zabraňuje přenosu DNA v PCR reakcích.

S1 Nuclease is an endonuclease which degrades single-stranded DNA and RNA.

B buffer for 100% activity Blue/white certified FastDigest buffer for 100% activity G buffer for 100% activity High concentration available LO certified O buffer for 100% activity Recombinant enzyme  Recombinant enzyme Tango buffer for 100% activity Thermal inactivation at 65°C in 10 min T4 DNA Ligase catalyzes the formation of phosphodiester bonds between 5‘-P and 3‘-OH of dsDNA fragments.

LO certified Recombinant enzyme Thermal inactivation at 70°C in 10 min T4 RNA Ligase catalyzes the ATP-dependent formation of phosphodiester bonds between 5'-P and 3'-OH termini of oligonucleotides, single-stranded RNA and DNA.

RNase A/T1 Mix combines the RNA degradation activity of both RNase A and RNase T1.

B buffer for 100% activity Blue/white certified FastDigest buffer for 100% activity G buffer for 100% activity High concentration available                                        LO certified O buffer for 100% activity Recombinant enzyme R buffer for 100% activity Tango buffer for 100% activity Thermal inactivation at 65°C in 10 min T4 DNA Ligase catalyzes the formation of phosphodiester bonds between 5‘-P and 3‘-OH of dsDNA fragments.

An endonuclease that nonspecifically cleaves single- and double-stranded DNA to release di-, tri-, and oligonucleotides with 5'-phosphate and 3'-OH groups.