
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fibrinogen α CRISPR/Cas9 KO Plasmid (h) | sc-400793 | 20 µg | $397.00 |
FGA encodes the fibrinogen α chain, a liver-derived secreted glycoprotein that assembles with the β and γ chains to form fibrinogen, the soluble precursor of fibrin. Upon vascular injury, thrombin-mediated cleavage of fibrinogen initiates polymerization and crosslinking events that stabilize clots and support platelet adhesion within the coagulation cascade. Fibrin(ogen) also participates in extracellular matrix remodeling and inflammatory signaling through interactions with integrins and other receptors, linking hemostasis to wound repair. Altered FGA function or expression is associated with quantitative or qualitative fibrinogen abnormalities that affect clot formation and can modify thrombotic or bleeding phenotypes, making it relevant for studies of coagulation biology and vascular inflammation.
Fibrinogen α CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the FGA gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the FGA 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 FGA 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 Fibrinogen α protein expression.
This CRISPR knockout system enables efficient generation of FGA-deficient cell models for investigation of Fibrinogen α 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.