
CRISPR knockout cell lines are engineered through targeted genome editing to eliminate gene function, supporting studies of cellular biology, disease mechanisms, and drug discovery.
ZNF395 (zinc finger protein 395) encodes a zinc finger protein with sequence-specific DNA-binding activity at RNA polymerase II cis-regulatory regions. It functions as a transcriptional activator and positively regulates RNA polymerase II-dependent transcription. ZNF395 is localized in the cytosol and nuclear speck, suggesting roles in transcriptional regulation and associated nuclear 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 2
Reference Transcript: NM_018660
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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