
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.
NOX5 (NADPH oxidase 5) encodes an NADPH oxidase that generates superoxide anions and has proton channel activity. It contributes to reactive oxygen species production, proton transport across membranes, and endothelial cell proliferation. NOX5 localizes to the plasma membrane and endoplasmic reticulum, where it can contribute to cellular redox signaling.
The MC3T3-E1 cell line is a foundational mouse osteoblast model derived from the cranial calvaria of newborn C57BL/6 mice. As referenced in image_2ede08.png, a series of subclones were isolated from the cloned but phenotypically heterogeneous parental MC3T3-E1 line to select for varying degrees of osteoblast differentiation and mineralization potential. This adherent line serves as a gold-standard in vitro platform for studying bone morphogenesis, osteogenesis pathway kinetics, and transcriptional regulation during matrix calcification.
Before delivery, each clone is authenticated by STR, tested for sterility and mycoplasma, and genotype‑verified by two‑round PCR‑sequencing. Comprehensive QC data accompany every shipment to support reproducible research.

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: E1
Reference Transcript: Notum-202
Frameshift Mutation Strategy
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?