
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
PLC β1 CRISPR/Cas9 KO Plasmid (h) | sc-401141 | 20 µg | $397.00 |
PLCB1 encodes phospholipase C beta 1 (PLCβ1), a G protein–regulated effector enzyme that hydrolyzes phosphatidylinositol 4,5-bisphosphate to generate inositol 1,4,5-trisphosphate and diacylglycerol, thereby mobilizing intracellular Ca2+ and activating protein kinase C signaling. This pathway integrates inputs from GPCRs to regulate diverse processes including neuronal excitability, synaptic signaling, secretion, and cytoskeletal dynamics. PLCβ1 activity contributes to downstream MAPK and calcium-dependent transcriptional programs, linking membrane receptor signaling to changes in gene expression and cellular state. Altered PLCB1 expression or signaling has been associated with neuropsychiatric phenotypes and aberrant growth-control signaling, supporting its use in mechanistic studies of signal transduction and disease-relevant cellular models.
PLC β1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the PLCB1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the PLCB1 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 PLCB1 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 PLC β1 protein expression.
This CRISPR knockout system enables efficient generation of PLCB1-deficient cell models for investigation of PLC β1 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.