RNase R

SKU:BHZ10900085
Research Validated
Overview
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RNase R (abm E049) is an E. coli 3′→5′ exoribonuclease that digests nearly all linear RNA while sparing circular RNA, lariat RNA and duplexes with short 3′ overhangs. Removing linear species from total RNA enriches circRNA for RNA sequencing. Supplied as 500 U (10 U/µl) with 10X RNase R Reaction Buffer.
circRNA Selectivity Spares closed-circular RNA
Stability 1 year from shipping date
Bundle Available Cat. E049-G138S with RNaseOFF
Options selector
Catalog no. Size
E049 500 U (50 ul)
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 500 U (50 ul)
  • Lead time: options listed in "Availability Content"; other statuses may take longer.
  • Storage: Store all components at -20 °C. Avoid repeated freeze-thaw cycles of all components to retain maximum performance. All components are stable for 1 year from the date of shipping when stored and handled properly.
  • Shipping: Please contact us to confirm shipping conditions for this product.
  • Upon receipt: store at recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Applications
  • Gene Expression
  • Enzyme Activity
Storage Store all components at -20 °C. Avoid repeated freeze-thaw cycles of all components to retain maximum performance. All components are stable for 1 year from the date of shipping when stored and handled properly.
Catalog no. (Mfr.) E049
Main SKU BHZ10900085

RNase R is an E. coli exoribonuclease that exhibits 3'-to-5' exonuclease activity, efficiently digesting nearly all linear RNA species. This enzyme does not digest circular, lariat, or double-stranded RNA with short 3’ overhangs (less than seven 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.

Product Component Quantity
RNase R (10 U/µl) 50 µl
10X RNase R Reaction Buffer 1.0 ml
Specification Value
Enzyme Type RNase (exoribonuclease)
Format Enzyme Only
Exonuclease Activity 3'→5' exoribonuclease
Substrate Selectivity Degrades linear RNA; spares circular, lariat and dsRNA with 3' overhangs <7 nt
Storage Conditions Store all components at -20 °C. Avoid repeated freeze-thaw cycles of all components to retain maximum performance. All components are stable for 1 year from the date of shipping when stored and handled properly.
Q.What is the substrate specificity of this enzyme?
A.RNase R is a 3′→5′ exoribonuclease that digests nearly all linear RNA species. It does not digest circular RNA, lariat RNA, or double-stranded RNA with 3′ overhangs shorter than seven nucleotides. That selectivity is what makes it the enzyme of choice for enriching circular RNA.
Q.What is it typically used for?
A.Removing linear RNA from cellular or RNA extracts so that circular species can be identified by RNA sequencing, and studying lariat RNA produced by traditional splicing alongside circRNAs that arise through back-splicing.
Q.Should I add an RNase inhibitor alongside it?
A.Protecting the surviving circRNA from contaminating RNases is worthwhile. A lot pairing this enzyme with RNaseOFF Ribonuclease Inhibitor is available as Cat. No. E049-G138S.
Q.What is supplied with this product?
A.50 µl of RNase R (10 U/µl) with 1.0 ml of 10X RNase R Reaction Buffer.
Q.How should I store this product?
A.Store all components at -20°C and avoid repeated freeze-thaw cycles to retain maximum performance. All components are stable for 1 year from the date of shipping when stored and handled properly.

De Tomi E, Orlandi E, Belpinati F, et al. (2024) New axes of interaction in the circ_0079593/miR-516b-5p network in melanoma metastasis cell lines. Genes, 15, 1647. 10.3390/genes15121647

Hu Q, Zhao H, Zhou K, et al. (2025) Scarless circular mRNA-based CAR-T cell therapy elicits superior antitumor efficacy. Signal Transduction and Targeted Therapy, 10, 411. 10.1038/s41392-025-02512-4

Wesselhoeft RA, Kowalski PS, Parker-Hale FC, et al. (2019) RNA circularization diminishes immunogenicity and can extend translation duration in vivo. Molecular Cell, 74, 508–520.e4. 10.1016/j.molcel.2019.02.015

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