
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
LAIR-1 CRISPR/Cas9 KO Plasmid (h) | sc-403542 | 20 µg | $397.00 |
LAIR1 encodes leukocyte-associated immunoglobulin-like receptor 1 (LAIR-1), an inhibitory collagen receptor broadly expressed on immune cells, including T cells, B cells, NK cells, monocytes, and dendritic cells. Upon binding extracellular matrix collagens, LAIR-1 signals through ITIM motifs to recruit phosphatases such as SHP-1/2, attenuating antigen receptor and Fc receptor pathways and constraining activation, cytokine production, and cytotoxicity. This checkpoint-like function links tissue matrix cues to immune homeostasis and influences leukocyte trafficking and inflammatory thresholds. Dysregulated LAIR-1 signaling has been associated with altered immune regulation in autoimmunity, chronic inflammation, infection, and tumor-associated immune suppression, making it a useful node for mechanistic immunology studies.
LAIR-1 CRISPR/Cas9 KO Plasmid (h) is a pool of plasmids designed for targeted disruption of the LAIR1 gene in human cell lines. Each plasmid co-expresses a unique single guide RNA (sgRNA) targeting a distinct site within the LAIR1 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 LAIR1 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 LAIR-1 protein expression.
This CRISPR knockout system enables efficient generation of LAIR1-deficient cell models for investigation of LAIR-1 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.