
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
CD33 CRISPR/Cas9 KO Plasmid (m2) | sc-419543-KO-2 | 20 µg | $397.00 |
Cd33 encodes CD33, a sialic acid–binding immunoglobulin-like lectin (Siglec) expressed primarily on myeloid lineage cells, where it functions as an inhibitory receptor that helps tune innate immune activation. Through immunoreceptor tyrosine-based inhibitory motifs (ITIMs), CD33 can recruit phosphatases such as SHP-1/SHP-2 to dampen signaling downstream of pattern-recognition receptors and other activating inputs, shaping cytokine production, phagocytosis, and inflammatory set points. In mouse systems, Cd33 is widely used to probe microglial and macrophage regulatory circuits, including sialylation-dependent “self” recognition and glyco-immune checkpoints. Altered CD33 activity and expression are associated with dysregulated myeloid responses in neuroinflammation and other immune-mediated disease contexts, making it a relevant node for mechanistic studies of immune homeostasis.
CD33 CRISPR/Cas9 KO Plasmid (m2) is a pool of plasmids designed for targeted disruption of the Cd33 gene in mouse cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the Cd33 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 Cd33 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 CD33 protein expression.
This CRISPR knockout system enables efficient generation of Cd33-deficient cell models for investigation of CD33 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.