Cellalabs provides an extensive array of CRISPR products and services tailored for both in vitro and in vivo genome editing experiments.
We offer a range of options from off-the-shelf reagents ready for gene delivery, to customized CRISPR vectors with high targeting efficiency and available in numerous delivery formats, including plasmid, lentivirus, AAV, adenovirus and RNA.
We focus on establishing the stable cell lines effectively even in the most difficult-to-transfect cells as well.
Besides, we are specialized in building uniquely designed and meticulously validated high-quality CRISPR libraries for gene knockout, inhibition, activation and other CRISPR screen purposes, which can serve as powerful tools for gene functional screens in both human and mouse.
Consistent High Editing Efficiency
Higher cutting and homologous recombination efficiency, 8-fold increase in gene-editing efficiency.
High Lot-to-lot Consistency
A large number of success case, successfully achieving over 3000 gene edits in over 150 cell line types.
Wide Application
Easily achieving gene knockout / point mutation / knock-in.
