
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.
ARHGAP20 (Rho GTPase activating protein 20) encodes a Rho GTPase-activating protein that regulates Rho-family GTPases by promoting conversion to their inactive GDP-bound state. ARHGAP20 functions downstream of RAP1 and can transmit RAP1 signaling to RHO, thereby influencing cytoskeletal dynamics and neurite outgrowth. Through regulation of Rho GTPase activity, ARHGAP20 may contribute to neuronal morphology and cellular signaling.
PC-3 is a human prostate cancer cell line established from a bone marrow metastasis of a poorly differentiated grade IV prostatic adenocarcinoma from a 62-year-old male patient after androgen suppression therapy. The cells are androgen-independent, exhibit low acid phosphatase and testosterone-5-alpha reductase activity, and are capable of growing in soft agar and forming tumors in nude mice. PC-3 is widely used as a model for studying advanced prostate cancer biology, androgen-independent tumor progression, metastasis, and anticancer drug development.
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.

Knockout Region: E1
Reference Transcript: AR-201
Validation Method: PCR amplification+Sanger sequencing
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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