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NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme (HMR)

The NEXTFLEX™ Cas9-gRNA rRNA Depletion Enzyme (HMR) powered by Jumpcode® DepleteX™ technology, is a standalone, workflow-agnostic depletion enzyme that removes ribosomal RNA sequences from human, mouse, or rat libraries. You can drop it into any bulk or single cell RNA-seq workflow, increasing usable reads for informative transcripts and improving coverage across the transcriptome.

NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme is provided at 5.6 μM and includes 435 unique guide RNAs targeting nuclear 5S, 5.8S, 18S, 28S, 45S and mitochondrial 12S and 16S rRNA loci. It requires a simple one-hour incubation making integration straightforward in pre- or post-PCR cleanup steps depending on your workflow. Designed to be highly cost-competitive and universally compatible, it delivers robust rRNA depletion without locking you into a specific library prep kit.

Feature Specification
Automation Compatible Yes
Product Group RNA Depletion

The NEXTFLEX™ Cas9-gRNA rRNA Depletion Enzyme (HMR) powered by Jumpcode® DepleteX™ technology, is a standalone, workflow-agnostic depletion enzyme that removes ribosomal RNA sequences from human, mouse, or rat libraries. You can drop it into any bulk or single cell RNA-seq workflow, increasing usable reads for informative transcripts and improving coverage across the transcriptome.

NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme is provided at 5.6 μM and includes 435 unique guide RNAs targeting nuclear 5S, 5.8S, 18S, 28S, 45S and mitochondrial 12S and 16S rRNA loci. It requires a simple one-hour incubation making integration straightforward in pre- or post-PCR cleanup steps depending on your workflow. Designed to be highly cost-competitive and universally compatible, it delivers robust rRNA depletion without locking you into a specific library prep kit.

Product variants
Unit Size: 50 μL
Part #:
NOVA-801100
List price
USD 500.00
Your online price:
Unit Size: 250 μL
Part #:
NOVA-801500
List price
USD 2,500.00
Your online price:
For research use only. Not for use in diagnostic procedures.

Overview

Ribosomal RNA can account for more than 90% of reads in total RNA sequencing libraries, making depletion essential for detecting low-abundance, biologically relevant transcripts. The NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme (HMR) is a cost-effective, workflow-independent, and highly specific enzyme that boosts usable reads without requiring you move to a new library prep kit. It implements a DASH (Depletion of Abundant Sequences by Hybridization) CRISPR depletion approach, using a precomplexed Cas9 and a pool of guides to cleave human, mouse, and rat rRNA sequences at the dsDNA stage. Whether you use your own prep method or a third-party kit, this module gives you clean, reproducible results backed by the performance of DepleteX™ technology.

  • Powered by Jumpcode™ technology for specific rRNA removal.
  • Ready-to-use: Provided as a Cas9-gRNA complex with integrated RNase inhibitor and Cas9 Buffer
  • Fast: Short one hour reaction time with only 5 minutes of hands-on time
  • Convenient: Easily fit into any library prep workflow
  • Flexible: Compatible with short and long-read sequencing
  • Automation-compatible – easily incorporated into manual or automated workflows

Additional product information

Cas9–gRNA-mediated targeted depletion

This kit applies Jumpcode® DepleteX™ technology to deplete rRNA sequences at the dsDNA stage, giving you flexibility in where the cut happens, either after second-strand synthesis or after library prep, depending on your workflow. The pre-complexed Cas9 and guide RNA pool targets conserved ribosomal RNA using 435 guides designed against GRCh38-annotated nuclear (5S, 5.8S, 18S, 28S, 45S) and mitochondrial (12S, 16S) rRNA. The pool has been functionally validated with good depletion performance in human, mouse, rat, dog and chicken libraries. Guides with predicted off-targets in protein-coding genes or other transcripts were remove to preserve informative content. This approach minimizes rRNA carryover and enhances the efficiency of total RNA sequencing without altering upstream chemistry.

A unit of NEXTFLEX Cas9-gRNA Depletion Enzyme is defined as the amount needed to deplete our recommended input of 1-10 ng of target dsDNA, assuming a library size of ≥400 bp (which typically corresponds to an insert of ~300 bp or greater).

Compatible with any RNA-seq strategy

Unlike depletion modules embedded in fixed library prep kits, this enzyme is completely workflow-agnostic. As long as you have double-stranded DNA, you can use it. By working at the dsDNA level, it sidesteps RNA input compatibility and integrates cleanly with existing RNA-seq workflows, no matter what reagents or sequencing downstream you're using.

Looking for a complete RNA-seq solution?

This depletion module is fully compatible with the NEXTFLEX Rapid Directional RNA-seq kits. Whether you’re working with intact samples or degraded RNA, Revvity offers RNA-seq workflows that deliver robust performance, high mapping rates, and flexible input requirements. Pair this module with a complete NEXTFLEX prep kit to streamline your workflow, improve data quality, and ensure end-to-end support from rRNA removal to sequencing-ready libraries.

Specifications

Automation Compatible
Yes
Product Group
RNA Depletion
Shipping Conditions
Shipped in Dry Ice
Unit Size
250 μL

FAQs

  • What are the benefits of using CRISPR-based ribodepletion solutions?
  • What is the benefit of depleting rRNA-derived fragments during library construction instead of before it?
  • What species are compatible with the NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme (HMR)?
  • What library prep kits are the NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme (HMR) compatible with?
  • Is the NEXTFLEX Cas9-gRNA rRNA Depletion Enzyme (HMR) compatible with degraded or fragmented RNA?
  • Is this compatible with DASH workflows?

Resources

Are you looking for resources, click on the resource type to explore further.

1-1 of 1 Resources
Application Note Icon
Application Note
Single‑cell gene fusion and rare event discovery with ribodepletion‑enhanced 10x–ONT sequencing.

This application note shows that the addition of a Cas9 based ribodepletion step markedly boosts information density in 10x ONT...

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