
Gene knockout cell lines are generated using CRISPR-Cas9 based technology to precisely disrupt target genes, enabling functional genomics research, disease modeling, and target validation.
ZNF133 (zinc finger protein 133) encodes a zinc finger transcriptional regulator predicted to bind DNA in a sequence-specific manner and regulate RNA polymerase II-dependent transcription. It is predicted to function primarily in the nucleus and to negatively regulate transcription by RNA polymerase II. These properties suggest that ZNF133 may contribute to control of gene expression through interactions with specific regulatory DNA sequences.
A human colon carcinoma cell line developed by Michael Brattain. The cells are derived from colon tissue and are classified as a cancer cell line.
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: EExon 5
Reference Transcript: NM_001283002
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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