
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.
The BeWo cell line was established from a malignant gestational choriocarcinoma of the fetal placenta and represents the first human trophoblastic endocrine cell type maintained in continuous culture. The cells exhibit trophoblastic characteristics and produce high levels of human chorionic gonadotropin (hCG), along with other placental hormones including placental lactogen and steroid hormones such as estrone, estradiol, estriol, and progesterone. BeWo cells can undergo cellular differentiation in response to hormonal precursors and are widely used as an in vitro model for studying trophoblast biology, placental hormone regulation, and mechanisms of placental development and function.
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: TRPV6-201
Validation Method: PCR amplification+Sanger sequencing
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use






Simply fill out the form below to leave your inquiry
— we will respond within 24 Hours
* Name
* Institution
* Products & Services of Interest
If email is not available, how else can we reach you?
How did you hear about us?