DNA/RNA modifying enzymes

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

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.

Available On-Site Highly thermostable DNA polymerase for routine PCR .

Available On-Site Highly thermostable DNA polymerase for routine PCR. .

Exonuclease I (ExoI) degrades single-stranded DNA in a 3'→5' direction, releasing deoxyribonucleoside 5'-monophosphates in a  stepwise manner and leaving 5'-terminal dinucleotides intact.

Highly thermostable DNA polymerase for routine PCR.

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

. Enhanced Taq DNA polymerase supplied with colored buffer enabling direct gel loading and significant time savings. Optimized for all standard PCR applications.

Enhanced Taq DNA polymerase supplied with colored buffer enabling direct gel loading and significant time savings. Optimized for all standard PCR applications. .

Exonuclease I (ExoI) degrades single-stranded DNA in a 3'→5' direction, releasing deoxyribonucleoside 5'-monophosphates in a  stepwise manner and leaving 5'-terminal dinucleotides intact.

Termosenzitivní alkalická fosfatáza katalyzuje odstraňování 5'- a 3'-fosfátových skupin z DNA, RNA, nukleotidů a proteinů.

RNase A is an endoribonuclease that specifically degrades single-stranded RNA at C and U residues.