
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
SPRED2 CRISPR/Cas9 KO Plasmid (h) | sc-404738 | 20 µg | $397.00 |
SPRED2 (sprouty related EVH1 domain containing 2) encodes a cytosolic adaptor protein that negatively regulates receptor tyrosine kinase signaling by inhibiting the Ras–Raf–MEK–ERK/MAPK cascade. Through interactions with components such as Raf and neurofibromin, SPRED2 helps constrain growth factor–driven proliferation, differentiation, and inflammatory signaling, contributing to homeostatic control of cellular responses. Altered SPRED2 expression or function has been linked to dysregulated MAPK activity in cancer biology and to immune and inflammatory processes, including contexts involving aberrant cytokine and chemokine signaling. As a pathway brake, SPRED2 is frequently studied for its role in tuning signaling amplitude and duration downstream of RTKs and other upstream inputs that converge on ERK.
SPRED2 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the SPRED2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the SPRED2 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 SPRED2 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 SPRED2 protein expression.
This CRISPR knockout system enables efficient generation of SPRED2-deficient cell models for investigation of SPRED2 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.