
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZBTB7B (zinc finger and BTB domain containing 7B) encodes a zinc finger transcription factor that regulates lineage commitment of immature T-cell precursors. It promotes commitment toward the CD4 T-cell lineage and, in its absence, favors CD8 lineage commitment. ZBTB7B also functions as a transcriptional repressor of type I collagen genes, linking its activity to both T-cell development and regulation of extracellular matrix-related gene expression.
The Caki-1 cell line was established in 1971 from a cutaneous metastasis of a kidney adenocarcinoma in a 49-year-old male patient. It is a human renal carcinoma cell line used as an in vitro model for studying kidney cancer biology and related molecular mechanisms.
Comprehensive quality control includes STR authentication, sterility testing (bacteria and fungi), and mycoplasma screening to ensure purity and performance. Genotype is confirmed by two rounds of PCR and Sanger sequencing, and complete validation reports are provided for make-to-order products.

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: EExon 5
Reference Transcript: NM_001377451
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?