
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
KHS CRISPR/Cas9 KO Plasmid (h) | sc-405817 | 20 µg | $397.00 |
Mitogen-activated protein kinase kinase kinase kinase 5 (MAP4K5), also known as kinase homologous to SPS1/STE20 (KHS), is a Ste20 family serine/threonine kinase that functions upstream of MAPK signaling modules. MAP4K5 contributes to stress-responsive and inflammatory signaling through regulation of JNK and related pathways, influencing transcriptional programs that control proliferation, apoptosis, and cytoskeletal dynamics. In human cells, KHS activity has been linked to modulation of innate immune responses and metabolic signaling, positioning MAP4K5 within broader networks that integrate receptor-mediated cues with kinase cascades. Dysregulated MAP4K5 signaling has been investigated in contexts such as oncogenic pathway rewiring and inflammatory disease mechanisms, supporting its use as a node for pathway dissection.
KHS CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the MAP4K5 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the MAP4K5 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 MAP4K5 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 KHS protein expression.
This CRISPR knockout system enables efficient generation of MAP4K5-deficient cell models for investigation of KHS 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.