
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Myosin Id CRISPR/Cas9 KO Plasmid (h) | sc-403425 | 20 µg | $397.00 |
MYO1D encodes Myosin Id, an actin-based, unconventional myosin implicated in organizing the cortical cytoskeleton and regulating membrane dynamics. Through interactions with actin filaments and membrane-associated complexes, MYO1D contributes to cell polarity, vesicle trafficking, and motility-related processes that influence tissue architecture. Altered MYO1D expression or function has been associated with dysregulated cytoskeletal remodeling and signaling networks linked to epithelial organization, migration, and tumor biology in several contexts. As a mechanochemical effector at the cell periphery, MYO1D is studied for its roles in coupling actin dynamics to membrane tension and directional transport.
Myosin Id CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the MYO1D gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the MYO1D 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 MYO1D 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 Myosin Id protein expression.
This CRISPR knockout system enables efficient generation of MYO1D-deficient cell models for investigation of Myosin Id 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.