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Base & Prime Editing

Built on high-quality editor mRNA and expertly engineered guide RNAs, IDT’s base and prime editing solutions help researchers achieve reliable precision editing performance and reproducible results across a wide range of applications.

Which editing approach is right for your application?

CRISPR-Cas9 editing, Base Editing, and Prime Editing represent complementary genome editing technologies, each using a distinct mechanism to introduce genetic changes. The table below provides an overview of the key steps in the editing process underlying each approach.

CRISPR-Cas9 Editing Base Editing Prime Editing
26-GE-Prime-Editing-Product-Page-GR-Cas9 26-GE-Prime-Editing-Product-Page-GR-Base 26-GE-Prime-Editing-Product-Page-GR-Prime

Mechanism:

  1. Target recognition: Cas9 guided by gRNA binds to target DNA
  2. DNA cleavage: Cas9 introduces a double-stranded break
  3. Cellular Repair: The break is repaired by NHEJ or HDR pathways

Mechanism:

  1. Target recognition: nCas9 guided by gRNA binds to the target DNA
  2. Deamination: The deaminase converts the target base within the editing window
  3. DNA nicking: nCas9 nicks the non-edited DNA strand to stimulate repair
  4. Base conversion: Cellular repair replaces the deaminated base, creating a precision conversion

Mechanism:

  1. Target recognition: Prime editor guided by pegRNA binds to the target DNA
  2. Nicking: Cas9 nickase cuts a single strand of the DNA
  3. Reverse transcription: The RT copies the edit encoded in the pegRNA RT template and incorporates it into the target DNA
  4. Repair: Edited strand is incorporated. The unedited strand is repaired to match new sequence
Feature CRISPR-Cas9 Base Editing Prime Editing
Double-strand DNA break required

Yes

No

No

Donor DNA template required

Often required for precise insertions

No

No

Supported edit types

Gene knockouts, insertions, and HDR-mediated modifications

A→G  and C→T base conversions

All base substitutions, small insertions, and deletions

Editing precision

Broad editing outcomes dependent on DNA repair pathways

Highly precise single-base changes

Precise sequence modifications with broad editing flexibility

Targeting flexibility

Broad target accessibility

Limited by editing window and PAM requirements

Broad edit capabilities across many genomic loci

Genotoxicity considerations

Higher due to double-strand break formation

Lower due to absence of double-strand breaks

Lower due to absence of double-strand breaks

Typical applications

Gene knockout, gene insertion, functional genomics

Precise nucleotide correction, disease modeling, translational research

Disease mutation correction, precision engineering, translational research

Design complexity

Relatively straightforward

Moderate

More complex due to pegRNA design requirements

Best used when

Creating knockouts or introducing larger insertions

Correcting specific point mutations with high precision

Installing precise substitutions, insertions, or deletions without donor DNA

RUO26-4591_001