
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
MISR II CRISPR/Cas9 KO Plasmid (h) | sc-402523 | 20 µg | $397.00 |
AMHR2 encodes the human anti-Müllerian hormone receptor type 2 (MISR II), a transmembrane serine/threonine kinase that binds AMH and initiates signaling via SMAD1/5/8 to regulate developmental programs in the Müllerian duct and gonadal differentiation. Receptor activation coordinates transcriptional responses involved in cell fate decisions, tissue remodeling, and reproductive tract maturation, integrating with broader TGF-β/BMP pathway dynamics. Dysregulated AMH–AMHR2 signaling has been associated with disorders of sexual development and reproductive endocrinology phenotypes, and altered MISR II expression has been investigated in ovarian-derived and other Müllerian lineage tumor contexts. As a pathway node, AMHR2 is useful for probing ligand-dependent receptor signaling, SMAD-mediated gene regulation, and context-specific growth and differentiation responses.
MISR II CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the AMHR2 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the AMHR2 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 AMHR2 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 MISR II protein expression.
This CRISPR knockout system enables efficient generation of AMHR2-deficient cell models for investigation of MISR II 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.