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Product description
Ribonuclease R (RNase R) is a magnesium-dependent 3'→5' exoribonuclease that can digest essentially all linear RNAs, but does not digest lariat or circular RNA structures, or double-stranded RNA with 3' overhangs shorter than 7 nucleotides. As such, this enzyme is ideally suited to the study of lariat RNA produced by traditional splicing, as well as circRNAs which arise through back-splicing. By removing linear RNAs from cellular or RNA extracts, RNase R greatly facilitates the identification of circular species through RNA-sequencing. This enables researchers to probe the landscape of splicing events with greater depth.
This product is produced in accordance with GMP process requirements and provided in liquid form.
Specifications
|
Expression Host |
Recombinant E. coli with RNase R gene |
|
Storage Buffer |
50 mM Tris-HCl, 100 mM NaCl, 0.1 mM EDTA, 1mM DTT, 0.1% TritonX-100,pH 7.5 |
|
Reaction Temperature |
37℃ |
|
Unit Definition |
One unit converts 1 μg of poly-r(A) into acid-soluble nucleotides in 10 minutes at 37 ℃. |
|
Application |
1.Identification of intronic lariat sequences 2.Identification of exonic circRNAs 3.Studying alternative splicing 4.Production of artificial circular RNAs |
Storage
This product should be stored at -25~-15℃ for two years.
Instructions
Experimental methods
|
Components |
Volume |
|
10 × RNase R Reaction Buffer* |
2 μL |
|
RNA Sample |
1 μg |
|
RNase R (20 U/μL) |
2-4 U |
|
DEPC H2O |
Up to 20 μL |
*According to the specific purpose of experiments, it is necessary to prepare the corresponding reaction buffer. You can consider buying 14616ES(10×RNase R Reaction Buffer GMP-grade) to use together.
Notes
1. Please operate with lab coats and disposable gloves,for your safety.
Ver.EN20240407
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