
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
COL9A2 CRISPR/Cas9 KO Plasmid (h) | sc-405890 | 20 µg | $397.00 |
COL9A2 encodes the α2 chain of type IX collagen, a FACIT collagen that associates with type II collagen fibrils to stabilize and organize the extracellular matrix of hyaline cartilage. By contributing to fibrillogenesis and matrix–cell interactions, COL9A2 supports chondrocyte function, cartilage tensile strength, and mechanotransduction processes central to skeletal development and joint homeostasis. Perturbation of COL9A2 expression or structure is linked to heritable cartilage disorders and has been studied in the context of early-onset degenerative joint phenotypes and intervertebral disc pathology. As a matrix component, COL9A2 connects extracellular matrix remodeling with pathways governing cartilage integrity, including collagen assembly, proteoglycan organization, and stress-responsive signaling in chondrocytes.
COL9A2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the COL9A2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the COL9A2 together with the Streptococcus pyogenes Cas9 nuclease. The plasmids also encode GFP, allowing fluorescent identification and enrichment of successfully transfected cells by fluorescence microscopy or flow cytometry.
The multi-guide design increases the likelihood of generating insertions or deletions (indels) that disrupt the COL9A2 open reading frame following Cas9-mediated double-strand break formation. DNA breaks introduced by the CRISPR/Cas9 system are repaired through endogenous non-homologous end joining (NHEJ) pathways, frequently resulting in frameshift mutations that abolish COL9A2 protein expression.
This CRISPR knockout system enables efficient generation of COL9A2-deficient cell models for investigation of COL9A2 signaling, functional genomics studies, cancer biology research, and evaluation of therapeutic responses in human cell lines.
CRISPRs +/- HDRs
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.