
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
apoH CRISPR/Cas9 KO Plasmid (m) | sc-419168 | 20 µg | $397.00 |
Apoh encodes apolipoprotein H (apoH; β2-glycoprotein I), a circulating phospholipid-binding glycoprotein that associates with anionic membranes and lipoprotein particles. In mice, apoH participates in lipid transport and clearance processes and interfaces with coagulation-related and complement-associated pathways through its interactions with negatively charged phospholipids exposed during cellular activation or damage. Altered APOH/apoH biology is linked to dysregulated hemostasis and inflammatory vascular processes, and it is frequently studied in the context of autoantibody-mediated phospholipid recognition. These functions make Apoh a useful target for investigating lipid–immune crosstalk, membrane-binding protein biology, and mechanisms that connect inflammation to thrombosis-related phenotypes in experimental models.
apoH CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Apoh gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Apoh 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 Apoh 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 apoH protein expression.
This CRISPR knockout system enables efficient generation of Apoh-deficient cell models for investigation of apoH 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.