RNase R

Product Information

Product description: Ribonuclease R (RNase R) from E. coli, is a magnesium-dependent 3' to 5' exoribonuclease that digests essentially all linear RNAs but does not digest lariat or circular RNA structures, or double-stranded RNA with 3'-overhangs shorter than 7 nucleotides. RNase R digests RNA from the 3' to 5' direction, releasing 5'-monophosphate nucleotides to produce dinucleotide and trinucleotide end products.

Resource: Recombinant E.coli

Concentration: 20U/μL

Unit Definition: One unit converts 1μg of poly-r(A) into acid-soluble nucleotides in 10 minutes at 37℃.

Storage Buffer: 50mM Tris-HCl, 0.1mM EDTA, 100mM NaCl, 1mM DTT, 0.1%(v/v)Triton X-100, 50%(v/v) glycerol, pH7.5@25℃.

Key points of operation

T4 RNA ligase 1, T4 RNA ligase 2, RNaseR on enzymatic synthesis of circular RNA:

IVT reaction to obtain linear RNA: it is worth noting that for this step of IVT reaction, a certain proportion of GMP needs to be doped to obtain GMP-containing linear RNA;

RNA cyclisation: circular RNA is produced by joining the two ends within the RNA molecule by T4 RNA ligase 1 (T4 Rnl1) or T4 RNA ligase 2 (T4 Rnl2) catalysing the joining of 5'-phosphate and 3'-hydroxyl groups at the RNA terminus;

Removal of linear RNA: RNaseR is able to remove all linear RNA molecules from the reaction solution, resulting in linear RNA-free circular RNA.

Security Information

Storage Conditions: Stored at -20±5°C.

Do not store in a frost-free freezer. Always avoid freeze-thaw cycles or exposure to frequent temperature changes. These fluctuations can greatly alter product stability.

Quality Assurance:

1. Functional Assay: Passes the internal function testing.
2. Contaminant Assay: Free of detectable Endonuclease and Exonuclease.
3. Endotoxin Assay: Pass.
4. Physical Purity: >95% by SDS-PAGE with Coomassie® blue staining.