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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
Synthetic peptide of Human GPR65
- 亚型:
IgG
- 形态:
Liquid
- 保存条件:
Upon receipt, store at -20℃ or -80℃. Avoid repeated freeze.
- 克隆性:
/
- 标记物:
Non-conjugated
- 适应物种:
Human
- 保质期:
6个月
- 抗原来源:
Homo sapiens (Human)
- 目录编号:
Q8IYL9
- 级别:
优
- 库存:
200
- 供应商:
武汉华美生物工程有限公司
- 宿主:
Rabbit
- 应用范围:
ELISA,IHC;ELISA:1:1000-1:2000,IHC:1:25-1:100
- 浓度:
>95%,Antigen affinity purification
- 靶点:
GPR65
- 抗体英文名:
GPR65 Antibody
- 抗体名:
GPR65;TDAG8;Psychosine receptor;G-protein coupled receptor 65;T-cell death-associated gene 8 protein
- 规格:
100μl/50μl
| 规格: | 100μl | 产品价格: | ¥1980.0 |
|---|---|---|---|
| 规格: | 50μl | 产品价格: | ¥1100.0 |
保存缓冲液
-20℃, pH7.4 PBS, 0.05% NaN3, 40% Glycerol功能
TDAG8 (for T-cell death-associated gene 8) is a seven transmembrane G protein-coupled receptor (GPCR) that was originally identified from a human thyroid cDNA library and subsequently shown to be expressed predominantly in thymus, lymph nodes, peripheral blood leukocytes and spleen. TDAG8, which is alternatively designated GPCR25, is grouped collectively with other GPCRs that are induced during T cell receptor engagement-mediated apoptosis and T cell activation, which also include G2A (for G2 accumulation) and P2Y2 (for P2 nucleotide) receptor.风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验祝贺〖雅裕睿安〗成为Signalway Antibody(SAB)独家
Zhu''T Yu''et al.(2007) Serum-free u mouse embryo cells generate a self-sustaining feedback loop for an astrocyte marker protein and respond to cytokines and bisphenol A in accordance with the subtle difference in their differentiation state.Cell
,美国加州基因技术公司(Genentech)的Germaine Fuh和同事突变了HER2的抗体,然后在突变体中筛选出了能够同时绑定HER2和VEGF的变异。这是首次创造出能绑定到2种无关联蛋白的抗体。Fuh说:“这将开启双重标靶型疗法之门。” 重点研发抗体疗法的Genmab生物技术公司副总裁Paul Parren表示,结果令人吃惊。他说:“我们以前根本没有这样考虑过抗体,它让人不禁要猜测,这种分子是否也有可能在自然界中存在。” Variants of the Antibody
顶级学术杂志评为最佳科学突破,被视为癌症治疗药物的第三次革命。免疫疗法靶点是正常免疫细胞,激活人体自身的免疫系统来治疗癌症。 具有代表性的肿瘤免疫治疗是以 PD1 靶点的药物。 PD-1 PD-1(Programed death-1),程序性死亡受体,位于正常免疫T细胞表面,是一种重要的免疫抑制分子,由日本京都大学本庶佑教授于 1992 年发现。2013 年同样靶点 PD1 的两个新药物,施贵宝的 nivolumab (商品名:Opdivo)和默沙东的pembrolizumab(商品
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