CRISPR Knockout Cell Lines

Ready-to-use gene knockouts, without running the edit yourself

Go straight from gene of interest to a confirmed KO cell line in your assay of choice.

abm maintains a library of CRISPR knockout (KO) cell lines and offers a custom knockout service, helping researchers bypass sgRNA design, delivery optimization, clonal screening, and validation.

  • 2,000+ ready-to-use KO lines
  • Supporting QC data included
  • Popular human cell backgrounds
  • Custom KO service available
CRISPR fundamentals

What is CRISPR, and why does it matter for cell biology?

CRISPR-Cas9 is a gene editing system adapted from a natural bacterial immune defence. Bacteria store short fragments of DNA from viruses that once infected them in regions of their genome called CRISPR arrays (Clustered Regularly Interspaced Short Palindromic Repeats). When the same virus attacks again, the bacterium copies these fragments into guide RNAs that direct the Cas9 enzyme to cut the invader's DNA at a matching sequence, destroying it.

Researchers repurposed this system as a programmable editing tool. By designing a synthetic guide RNA that matches almost any DNA sequence, Cas9 can be directed to cut a specific gene inside a living cell rather than a virus. That ability to target a precise DNA sequence on demand is what makes CRISPR the most widely adopted genome editing platform in life science research today, replacing older, less efficient tools such as zinc finger nucleases and TALENs.

Key term

sgRNA (single guide RNA)

A short synthetic RNA sequence that matches the target gene and physically directs Cas9 to the correct location in the genome.

Key term

PAM site

A short DNA sequence adjacent to the target that Cas9 requires in order to bind and cut; it acts as a molecular checkpoint.

Key term

Double-strand break (DSB)

The cut Cas9 makes across both strands of the DNA helix at the target site.

Key term

NHEJ repair

Non-homologous end joining, the cell's default, error-prone repair pathway; the small insertions or deletions it introduces are what knock out the gene.

Four-stage workflow
How CRISPR Knockout Editing Works: a four-step workflow showing guide RNA design, Cas9 and sgRNA delivery, cut and repair, and screening and validation of knockout clones.
CRISPR knockout cell line generation—from guide design through validated single-cell clones.
Portfolio highlights

Everything you need to knock out a gene, without running the edit yourself

In stock

2,000+ ready-to-use KO lines

A continuously growing inventory of pre-made knockout cell lines available for immediate delivery, searchable by gene name, symbol, or accession number.

Custom service

Flat-fee knockout generation

Can't find your gene or cell line listed? abm generates a custom KO, regardless of cell line, covering design through validation.

Validation

QC data included with every line

Each knockout cell line arrives with supporting quality control data confirming the edit, so you can move straight into experiments.

Time savings

Faster than a DIY project

Skip sgRNA design, cloning, delivery optimization, and clonal screening, and start with a confirmed knockout instead.

Risk protection

Cell line insurance available

Protect your investment against growth issues, thawing failures, or freezer breakdowns with abm's optional Cell Line Insurance.

Build vs. buy

Generating a knockout in-house vs. ordering one from abm

DIY: In-house CRISPR editing

  • Design and validate sgRNAs from scratch
  • Source and troubleshoot Cas9 delivery reagents
  • Optimize transfection or transduction conditions
  • Isolate and screen single-cell clones by hand
  • Confirm the edit before starting your real experiment

abm: Ready-made or custom KO line

  • Select an in-stock KO line or request any gene/cell line combination
  • sgRNA design, delivery, and clonal screening handled for you
  • Delivered with supporting QC data confirming the knockout
  • Go straight into your assay, not another optimization project
FAQ

Common questions about CRISPR knockout cell lines

Learn how CRISPR knockout cell lines are generated, what is included with each line, and when a custom KO or Cas9-expressing background is the better fit.

What is a CRISPR knockout (KO) cell line?
A CRISPR knockout cell line is a cell line in which a specific gene has been permanently disabled using CRISPR-Cas9 gene editing, so the cell can no longer produce a functional copy of that gene's protein. Researchers use KO cell lines to study a gene's normal role by observing what changes once it is removed.
How does CRISPR-Cas9 gene editing work?
A short guide RNA directs the Cas9 enzyme to a matching DNA sequence next to a PAM site. Cas9 cuts both strands of DNA at that location, and the cell's own repair pathway reseals the break, often introducing small insertions or deletions that shift the gene's reading frame and knock out its function.
What's the difference between a CRISPR KO cell line and a Cas9-expressing cell line?
A CRISPR KO cell line already has a target gene permanently disrupted and is ready to use. A Cas9-expressing cell line stably expresses the Cas9 enzyme but has no gene knocked out yet; you add your own sgRNA afterward, which is useful when you want to screen several gene targets in the same genetic background.
Which cell backgrounds are available as ready-to-use KO cell lines?
abm's inventory of 2,000+ ready-to-use knockout cell lines spans popular backgrounds including HEK293, HEK293T, A549, HeLa, HepG2, MCF7, K562, and U-87 MG, with additional gene targets and backgrounds added on an ongoing basis.
Can I get a gene or cell line knocked out that isn't already listed?
Yes. abm's custom CRISPR knockout service covers any human gene in any cell line, including sgRNA design, delivery, clonal screening, and validation.
What quality control data comes with each knockout cell line?
Every knockout cell line is delivered with supporting QC data confirming the edit, so you can verify the knockout before you build it into your experimental design.
Why order a knockout instead of running the CRISPR edit myself?
In-house knockout generation involves sgRNA design, reagent optimization, delivery, single-cell cloning, and validation — work that can take significant hands-on lab time. Ordering a validated line removes that workload and its reagent costs, and abm's flat per-gene pricing is typically more cost-effective than sourcing the reagents for a DIY project.

Need to knock out more than one gene in the same background?

Start from an abm Cas9-expressing stable cell line and introduce your own sgRNA library or custom guide, ideal for multi-gene screens and knock-in projects that need a repair template.