
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
COL2A1 CRISPR/Cas9 KO Plasmid (h) | sc-400359 | 20 µg | $397.00 |
COL2A1 encodes the α1 chain of type II collagen, a major fibrillar collagen that forms the structural framework of hyaline cartilage and contributes to the biomechanical properties of the extracellular matrix. Through assembly into collagen II fibrils and interactions with proteoglycans, COL2A1 supports chondrocyte differentiation, matrix organization, and cartilage homeostasis during skeletal development. COL2A1 expression is regulated by chondrogenic transcriptional programs such as SOX9-driven pathways and coordinates with collagen processing, secretion, and extracellular matrix remodeling networks. Genetic disruption or dysregulation of COL2A1 is linked to a spectrum of heritable cartilage and skeletal disorders, making it a key target for studying extracellular matrix biology and chondrocyte pathology.
COL2A1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the COL2A1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the COL2A1 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 COL2A1 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 COL2A1 protein expression.
This CRISPR knockout system enables efficient generation of COL2A1-deficient cell models for investigation of COL2A1 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.