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T4 RNA ligase 2 HYJ237

T4 RNA Ligase 2, also known as T4 RNA Ligase 2, is an ATP-dependent double-stranded RNA ligase (dsRNA Ligase), capable of performing both intramolecular circular ligation and intermolecular linear ligation of double-stranded RNA. 

Cat.No.:HYJ237

Specification:1KU/5KU

    T4 RNA Ligase 2, also known as T4 RNA Ligase 2, is an ATP-dependent double-stranded RNA ligase (dsRNA Ligase), capable of performing both intramolecular circular ligation and intermolecular linear ligation of double-stranded RNA. Unlike T4 RNA Ligase 1, T4 RNA Ligase 2 exhibits significantly greater ligation activity towards nicks within double-stranded RNA than towards the ends of single-stranded RNA. T4 RNA Ligase 2 can also be used to connect the 3' hydroxyl group of an RNA strand to the 5' phosphate group of a DNA strand, either intramolecularly or intermolecularly within double-stranded nucleic acids (RNA duplexes, RNA/DNA hybrids, or DNA duplexes). T4 RNA Ligase 2 requires both a 5' phosphate and a 3' hydroxyl group, enabling the ligation reaction between the 5' phosphate group of an RNA or DNA strand and the 3' hydroxyl group of an RNA strand. It is primarily used to connect nicks in double-stranded RNA (Double-stranded RNA sticky-end ligation). It can also be used to connect nicks in double-stranded structures, such as the 3' hydroxyl group of RNA and the 5' phosphate group of DNA. T4 RNA Ligase 2 is a recombinant protein expressed in Escherichia coli. The gene expressed is derived from the T4 bacteriophage.

    Components

    Components

    1KU

    5KU

    T4 RNA Ligase 2 (10U/µL)

    100 uL

    500 uL

    10× Reaction Buffer

    300 uL

    1.5 mL

    RNase-Free ddH2O

    1 mL

    5 mL

    Storage

    Store at -25 to -15°C. Valid for 1 years.

    Storage buffer

    10mM Tris-HCl(pH7.5), 50mM KCl, 35mM(NH4)2SO4, 0.1mM EDTA, 0.1mM DTT , 50% (v/v) Glycerol.

    Activity Definition

    One unit is defined as the amount of enzyme required to ligate 0.4 µg of an equimolar mixture of 23-mer and 17-mer RNAs in 20 µL at 37°C in 30 minutes.

    Quality Control

    1.Free of RNase and DNase contamination.

    2.T4 RNA Ligase 2 purity >90% as determined by Coomassie Brilliant Blue-stained SDS-polyacrylamide gel.

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