
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.
ZBTB45 (zinc finger and BTB domain containing 45) encodes a zinc finger and BTB domain-containing protein with sequence-specific double-stranded DNA-binding activity. The protein is predicted to function as a transcriptional regulator, including negative regulation of RNA polymerase II-dependent transcription. It is also predicted to regulate cytokine production and immune system processes and is primarily localized to the nucleus.
NCI-H1975 is a human non-small cell lung cancer cell line established from lung tumor tissue. The donor was a non-smoker. The cell line is used as a model for studying lung cancer biology and molecular mechanisms associated with non-small cell lung carcinoma.
Each knockout cell line is validated by STR authentication, sterility testing (bacteria/fungi), and mycoplasma screening. Genotype is confirmed by two rounds of PCR and Sanger sequencing. Only clones that pass all QC criteria are released, ensuring reliable identity and performance for downstream applications.

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_001316982
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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