
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CRELD2 CRISPR/Cas9 KO Plasmid (h) | sc-407369 | 20 µg | $397.00 |
CRELD2 (cysteine rich with EGF like domains 2) encodes an endoplasmic reticulum–resident, disulfide bond–containing protein implicated in protein quality control and secretory pathway homeostasis. CRELD2 expression is commonly induced during ER stress and is linked to unfolded protein response signaling, where it can influence proteostasis, redox balance, and secretion of client proteins. Through these processes, CRELD2 has been studied in contexts of cellular stress adaptation and inflammation-related signaling, and altered expression has been reported across multiple disease-relevant settings including cancer and metabolic or fibrotic phenotypes. As a modulator of ER-associated pathways, CRELD2 provides a tractable node for dissecting how stress-responsive secretory programs shape cell state and survival.
CRELD2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the CRELD2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the CRELD2 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 CRELD2 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 CRELD2 protein expression.
This CRISPR knockout system enables efficient generation of CRELD2-deficient cell models for investigation of CRELD2 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.