CD96抗體

英文名稱  Anti-CD96 
中文名稱  CD96抗體 
別    名  ANCO 1; ANCO1; Ankyrin repeat containing cofactor 1; Ankyrin repeat domain 11; Ankyrin repeat domain containing protein 11; LZ16; T13; ANR11_HUMAN. 
詳細介紹：

相關資料：

產品介紹 CD96 antigen, also designated T cell surface protein tactile (T cell activation, increased late expression) precursor, is a type I membrane protein and is a member of the immunoglobulin supergene family of proteins. The gene encoding for the CD96 protein maps to chromosome 3q13.13-q13.2. During the late phases of the immune response, CD96 is involved in adhesive interactions of activated, both helper and cytotoxic, NK and T cells. It interacts with CD155. CD96, shows increased expression after NK and T cell activation. It can also be found actively engaging diseased cells and moving in inflamed areas after NK and T cells have moved through the endothelium. CD96 is involved in antigen presentation and/or lymphocyte activation. The protein, which may form a homodimer, is expressed on normal T cell lines and some transformed T cells.
Function : May be involved in adhesive interactions of activated T and NK cells during the late phase of the immune response. Promotes NK cell-target adhesion by interacting with PVR present on target cells. May function at a time after T and NK cells have penetrated the endothelium using integrins and selectins, when they are actively engaging diseased cells and moving within areas of inflammation.
Subunit : Interacts with the PAS region of the p160 coactivators. 
Subcellular Location : Membrane.
Tissue Specificity : Expressed on normal T-cell lines and clones, and some transformed T-cells, but no other cultured cell lines tested. It is expressed at very low levels on activated B-cells.
DISEASE : Defects in CD96 are a cause of C syndrome (CSYN) [MIM:211750]; also called Opitz trigonocephaly syndrome. This syndrome is characterized by trigonocephaly and associated anomalies, such as unusual facies, wide alveolar ridges, multiple buccal frenula, limb defects, visceral anomalies, redundant skin, psychomotor retardation and hypotonia. Note=A chromosomal aberration involving CD96 has been found in a patient with C syndrome. Translocation t(3;18)(q13.13;q12.1). CD96 gene was located at the 3q13.13 breakpoint. Precise structural analysis around the breakpoint showed that the gene was disrupted by the translocation in exon 5, probably leading to premature termination or loss of expression of CD96 protein. No gene was detected at the chromosome 18 breakpoint.
Defects in CD96 are a cause of C-like syndrome (CLSYN) [MIM:605039]; also called Opitz trigonocephaly-like syndrome. The C-like syndrome seems to be a severe form of the C syndrome. It is controversial whether there is (1) a gradient of spectrum in the C syndrome, from the mild form (C syndrome) to the severe form (C-like syndrome), or (2) genetic heterogeneity among the patients with the C syndrome.
Similarity : Contains 1 Ig-like C2-type (immunoglobulin-like) domain.
Contains 2 Ig-like V-type (immunoglobulin-like) domains.
Database links : UniProtKB/Swiss-Prot: Q6UB99.3