
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF12 (zinc finger protein 12) encodes a nuclear transcriptional regulator containing a KRAB domain and eight C2H2-type zinc fingers. Through its DNA-binding zinc finger domains, ZNF12 is involved in developmental control of gene expression. The KRAB domain supports transcriptional regulatory activity, suggesting that ZNF12 contributes to repression or modulation of specific gene expression programs during cellular and developmental processes.
T98G is a human glioblastoma multiforme cell line derived from a tumor of a 61-year-old male patient. The cells exhibit an indefinite lifespan and anchorage-independent growth properties, while retaining the ability to enter a viable G1-arrested state under serum deprivation conditions. T98G is used as a model for studying glioblastoma biology, cell cycle regulation, tumor growth mechanisms, and therapeutic responses.
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 3
Reference Transcript: NM_006956
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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