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Mouse GITR/TNFRSF18 MAb (Clone 108626) (500 UG)

货号: MAB524 基本售价: 5026.6 元 规格: 500 ug

产品信息

概述
货号MAB524
描述For ELISA the Antibody Pairs information:Capture antibody:MAB524;Detection antibody:BAF524; and protein: 524-GR-050
别名Activation-inducible TNFR family receptor; AITR; AITRTNF receptor superfamily activation-inducible protein; CD357 antigen; CD357; GITR-D; GITRtumor necrosis factor receptor superfamily member 18; Glucocorticoid-induced TNFR-related protein; TNFRSF18; tumor necrosis factor receptor superfamily, member 18
全称Glucocorticoid Induced TNF Receptor Family Related Gene
反应种属Mouse
应用Western Blot,ELISA Capture (Matched Antibody Pair),ELISA Detection (Matched Antibody Pair),ELISA Standard
目标/特异性Detects mouse GITR/TNFRSF18 in ELISAs and Westen blots. In direct ELISAs, no cross-reactivity with recombinant human (rh) 4-1BB, recombinant mouse (rm) 4-1 BB, rhCD27, rmCD27, rhCD30, rmCD30, rhCD40, rmCD40, rhDR3, rhDR6,rhEDAR, rmEDAR, rhFas, rmFas, rhGITR, rhHVEM, rhLT beta R, rmLT beta R, rhNGF R, rhOPG, rmOPG, rhRANK, rmRANK, rhTROY, rmTROY, rhTNF R1, rmTNF R1, rhTNF R2, or rmTNF R2 is observed.
使用方法Western Blot: 1 µg/mL
ELISA Capture (Matched Antibody Pair): 2-8 µg/mL 
ELISA Detection (Matched Antibody Pair): 0.1-0.4 µg/mL 
ELISA Standard :  
来源Reconstitute at 0.5 mg/mL in sterile PBS.
产品组分
性能
供应商R&D Systems
Entrez Gene IDs8784 (Human); 21936 (Mouse); 500598 (Rat); 102146362 (Cynomolgus Monkey)
纯化方式Protein A or G purified from hybridoma culture supernatant
免疫原Mouse myeloma cell line NS0-derived recombinant mouse GITR/TNFRSF18
Gln20-His153 (predicted)
Accession # O35714
生物活性Mouse
标记Unconjugated
溶解方法Reconstitute at 0.5 mg/mL in sterile PBS.
背景

GITR (glucocorticoid-induced tumor necrosis factor receptor; also named AITR) is a member of the co‑stimulatory subset of the TNF receptor superfamily (1, 2). In mouse, the GITR gene is composed of five exons and encodes multiple length isoforms that arise from alternate splicing. The “standard”, or first reported isoform is a type I transmembrane protein, 228 amino acids (aa) in length that contains a 19 aa signal sequence, a 134 aa extracellular region, a 21 aa transmembrane segment, and a 54 aa cytoplasmic domain. The extracellular region contains four potential N-linked glycosylation sites plus three cysteine-rich pseudorepeats of about 40 aa each (3, 4). The extracellular regions of mouse and human are 57% aa identical. The cytoplasmic domain has a P-x-Q/E-E motif that is known to associate with TRAF2. This is a common characteristic of TNFRSF members with co‑stimulatory functions (4). Three other mouse GITR isoforms (B, C and D) have been reported (5). All share the same N-terminal 101 of 134 aa in the extracellular region (including pseudorepeats #1, #2 and one-half of #3). Isoform D diverges at aa 101 and continues for another 12 aa for a total length of 113 aa. This is a naturally-occurring soluble form. Isoforms B and C show splicing in their cytoplasmic tails that creates cytoplasmic domains of 118 aa and 46 aa, respectively. In both the B and C isoforms, the TRAF2 binding site is spliced out, with a p56lck binding site inserted in isoform B (4). Given its membership in the TNFRSF, it likely functions as a trimer on the cell surface (2). GITR is predominantly expressed on CD4+CD25+ regulatory T cells (Treg) and naïve CD8+ and CD4+CD25- T cells, where its expression is up-regulated after antigen-driven activation. GITR activation provides co‑stimulatory signals for activated CD4+ CD25- T cells to enhance cell proliferation and augment cytokine production (IL-2, IL-4, IFN-gamma ). On CD4+CD25+ Treg cells, GITR activation provides co‑stimulatory signals to induce proliferation, setting Treg cells in an active/hyperproliferactive state (6‑8).

运输条件Blue Ice
存放说明-20℃
参考文献
  1. Kwon, B. et al. (2003) Exp. Mol. Med. 35:8. 
  2. Croft, M. (2003) Nat. Rev. Immunol. 3:609. 
  3. Nocentini, G.et al. (1997) Proc. Natl. Acad. Sci. USA 94:6216.
  4. Nocentini, G. et al. (2000) DNA Cell Biol. 19:205. 
  5. Nocentini, G. et al. (2000) Cell Death Differ. 7:408.
  6. Tone, M. et al. (2003) Proc. Natl. Acad. Sci. USA 100:15059.
  7. Ji, H. et al. (2004) J. Immunol. 172:5823.
  8. Stephens, G.L. et al. (2004) 173:5008.