CRISPR Cas9 Gene Editing - CRISPR Library Screening - Gene Knockout Cell Line - Knock in Cell Line - Cas12a

Kickstart 2026 with In-Stock CRISPR Cell Lines — Starting from $1,600

Start the new year with speed, precision, and confidence!

To support your early-stage research planning in 2026,EDITGENE is offering a New Year special on hot spot, hot-in-research in-stock cell lines.

For a limited time, our SLCs, HAP1, and point mutation in-stock models are available for as low as $1600, helping you move faster without compromising data quality.

▎Why In-Stock Models?

Custom projects are powerful, but they take time.
Our in-stock cell lines are designed for teams who need to:

● Start assays immediately (screening, validation, mechanism studies)

● De-risk larger projects with pilot experiments

● Access high-quality, fully QC’d models without long lead times

● Stretch limited budgets while maintaining scientific rigor

Each in-stock cell line includes:

● Full QC documentation (Sanger sequencing, mycoplasma-free, STR available on request)

● Detailed project report

● 2 vials per line, with standardized cell numbers per vial

Hotspot Point Mutation Cells

HAPPY NEW YEAR

Precision Modeling of Disease-Critical Mutations

Single-nucleotide variants (SNVs) drive disease onset, progression, drug response, and protein function changes.

Our Prime Editing–based hotspot point mutation lines allow you to study mutation-driven mechanisms at single-base resolution, without additional indels or exogenous scars.

At EDITGENE, these Prime Editing cell lines are developed using our proprietary Bingo™ platform , ensuring:

● Scarless, highly precise base changes
● Consistent editing performance
● Standardized QC workflows across all in-stock models

Key features:
86+ high-demand disease-relevant point mutation sites

Built on a validated Prime Editing system

In stock · ready to ship

Free WT control included

Ideal for:
● Mechanistic studies of pathogenic variants
● Target validation & functional genomics
● Drug sensitivity & resistance modeling
● Biomarker discovery and assay development

Explore Our Hotspot Point Mutation Portfolio Below:

SLCs in the Spotlight

HAPPY NEW YEAR

Decoding Drug Transport, Distribution, and Resistance with SLCs

Solute carrier (SLC) transporters play a central role in drug uptake, intracellular distribution, and resistance across oncology, metabolic disease, and pharmacogenomics research.

Disrupting key transporters, such as SLC22A1 (OCT1) and SLC47A1 (MATE1) allows researchers to directly dissect transporter-dependent drug behavior, map intracellular exposure, and evaluate transporter-mediated resistance mechanisms.

At EDITGENE, our SLC knockout models are generated using optimized CRISPR/Cas9 strategies and rigorous multi-layer validation, delivering stable, reproducible loss-of-function systems suitable for mechanistic pharmacology and translational studies.

● Targeting key SLC family transporters

● Optimized for drug transport, metabolism & resistance research

● Fully QC-validated (Sanger, sterility, mycoplasma-free)

● Free WT control included

Ideal applications include:

● Drug transport & uptake pathway validation

● Pharmacokinetic & intracellular exposure modeling

● Drug resistance mechanism studies

● Transporter–drug interaction profiling

● Synthetic lethality & pathway dependency mapping

Explore Our In-Stock SLC Knockout Lines Here:

HAP1 Knockout Cell Lines

HAPPY NEW YEAR

A Haploid Platform for Unambiguous Functional Genomics

The haploid genome of HAP1 cells allows mutations to be expressed at the phenotypic level without allelic masking, enabling direct, unambiguous genotype, phenotype correlation. This makes HAP1 an exceptionally powerful platform for loss-of-function studies, pathway analysis, and CRISPR-based functional genomics.

At EDITGENE, we leverage the unique advantages of the HAP1 system to generate precisely engineered and fully validated knockout models with highly consistent editing outcomes. These ready-to-use models support functional validation, dependency mapping, phenotypic screening, and mechanism-of-action studies; all with clearer read-through to biology.

● Haploid background for clean functional readouts

● Ideal for pathway analysis & phenotypic screening

● A time-saving alternative to custom model generation

● Free WT control included

Explore Our HAP1 Knockout Cell Lines Here:

Ready to accelerate your research with in-stock engineered cell lines?
Start off the year strong, and let’s move your project from planning to data; faster, simpler, and with confidence.

Order Now!

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