
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
c-Mpl CRISPR/Cas9 KO Plasmid (h) | sc-403035 | 20 µg | $397.00 |
MPL encodes the thrombopoietin receptor c-Mpl, a type I cytokine receptor expressed predominantly in hematopoietic stem/progenitor cells and the megakaryocytic lineage where it regulates self-renewal, survival, and platelet production. Ligand engagement activates JAK2-dependent signaling with downstream STAT, PI3K/AKT, and MAPK/ERK pathways that coordinate proliferation and differentiation programs in the bone marrow niche. Dysregulated MPL signaling and altered receptor function are associated with abnormal megakaryopoiesis and myeloid disease biology, including phenotypes linked to aberrant cytokine responsiveness and stem cell homeostasis. As a lineage-restricted receptor with well-defined pathway outputs, c-Mpl serves as a tractable node for dissecting cytokine signaling, hematopoietic fate decisions, and receptor-mediated feedback control.
c-Mpl CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the MPL gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the MPL 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 MPL 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 c-Mpl protein expression.
This CRISPR knockout system enables efficient generation of MPL-deficient cell models for investigation of c-Mpl 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.