anti-KIR2DL1 Antibody from antibodies-online

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anti-KIR2DL1 Antibody

Description

Product Characteristics:
The KIR family consists of transmembrane glycoproteins of the Ig superfamily expressed on natural killer (NK) cells and a subset of human T cells. KIR2DL1 is a receptor on human NK cells for HLA-C alleles. It inhibits the activity of NK cells thus preventing cell lysis.

Subcellular location: Cell membrane

Synonyms: Killer cell immunoglobulin-like receptor 2DL1, CD158A, Killer cell immunoglobulin like receptor 2DL1, MHC class I NK cell receptor, Natural killer associated transcript 1, NKAT 1, NKAT-1, NKAT1, p58 natural killer cell receptor clones CL-42/47.11, p58 NK receptor, p58.1 MHC class I specic NK receptor, CD158 antigen-like family member A, KI2L1_HUMAN, Natural killer-associated transcript 1, p58 NK receptor CL-42/47.11, p58.1 MHC class-I-specic NK receptor, CD158a.

Target Information: Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets of T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content of the KIR gene cluster varies among haplotypes, although several 'framework' genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number of extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets of HLA class I molecules\\\\, thus, KIR proteins are thought to play an important role in regulation of the immune response. [provided by RefSeq, Jul 2008]