
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
The RAW 264.7 cell line was established from the ascites of a tumor induced in a male mouse by intraperitoneal injection of Abelson murine leukemia virus (A-MuLV). This murine macrophage-like cell line exhibits functional characteristics associated with macrophages, including pinocytosis of neutral red, phagocytosis of zymosan particles, and antibody-dependent lysis of target cells. RAW 264.7 cells are responsive to lipopolysaccharide (LPS), which inhibits cell growth, and are widely used as an in vitro model for studying macrophage activation, innate immune responses, inflammatory signaling, and related immunological processes.
Before delivery, each clone is authenticated by STR, tested for sterility and mycoplasma, and genotype‑verified by two‑round PCR‑sequencing. Comprehensive QC data accompany every shipment to support reproducible research.

Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations
These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.
Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.

Targeted knockout region: E2
Reference Transcript: Fabp5-201
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use




Simply fill out the form below to leave your inquiry
— we will respond within 24 Hours
* Name
* Institution
* Products & Services of Interest
If email is not available, how else can we reach you?
How did you hear about us?