
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
α1D-AR CRISPR/Cas9 KO Plasmid (m) | sc-419022 | 20 µg | $397.00 |
Adra1d encodes the mouse α1D-adrenergic receptor (α1D-AR), a G protein-coupled receptor that primarily couples to Gq/11 to stimulate phospholipase C signaling, inositol phosphate production, intracellular Ca2+ mobilization, and PKC activation. Through these pathways, α1D-AR influences smooth muscle contraction, vascular and urinary tract tone, and broader autonomic regulation, with downstream effects on MAPK/ERK signaling and transcriptional programs. Adra1d expression and signaling dynamics are frequently examined in the context of tissue-specific adrenergic responsiveness and receptor subtype contributions to physiological homeostasis. Dysregulated adrenergic GPCR signaling has been linked to cardiometabolic and neurobehavioral phenotypes in preclinical models, making Adra1d a relevant target for mechanistic studies of stress-responsive pathways.
α1D-AR CRISPR/Cas9 KO Plasmid (m) is a pool of plasmids designed for targeted disruption of the Adra1d gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Adra1d 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 Adra1d 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 α1D-AR protein expression.
This CRISPR knockout system enables efficient generation of Adra1d-deficient cell models for investigation of α1D-AR 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.