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SLAMF7

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For Research Use Only. Not For Clinical Use.


Background

SLAMF7, also known as CD319, is a cell surface glycoprotein belonging to the signaling lymphocytic activation molecule (SLAM) family. It is expressed on a variety of immune cells, including natural killer (NK) cells, T cells, and B cells, as well as on malignant plasma cells in multiple myeloma. SLAMF7 plays a role in cell adhesion, activation, and cytotoxicity. In particular, it is involved in the activation of NK cells and the enhancement of their cytotoxic activity against target cells. Because of its overexpression in multiple myeloma cells, SLAMF7 has become an attractive target for immunotherapy. Therapeutic antibodies targeting SLAMF7 have shown promising results in clinical trials, demonstrating their ability to induce direct tumor cell killing and enhance immune-mediated destruction of myeloma cells. Ongoing research aims to further elucidate the precise signaling pathways mediated by SLAMF7 and to optimize its use in the treatment of hematological malignancies.
SLAMF7
Protein class

CD markers, FDA approved drug targets

Predicted location

Intracellular, Membrane (different isoforms)

Single cell type specificity

Cell type enhanced (Plasma cells, monocytes, NK-cells, dendritic cells)

Immune cell specificity

Low immune cell specificity

Cell line specificity

Cell line enriched (U-266/70)

Interaction

Isoform 1 binds to SH2D1A when its cytoplasmic tail is phosphorylated in the presence of FYN (in vitro); low affinity binding, the physiological relevance of the interaction is questioned. Interacts with SH2D1B; in NK cells (PubMed:16339536). Interacts (via ITSM phosphorylated on Tyr-302) with SH2D1B, PTPN6/SHP-1, PTPN11/SHP-2, INPP5D/SHIP1, CSK and FYN (By similarity).

Molecular function

Receptor

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