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内皮抑素/内皮他丁抗体

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产物名称: 内皮抑素/内皮他丁抗体
产物型号:
产物展商: 单克隆抗体/多克隆抗体
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简单介绍

内皮抑素/内皮他丁抗体应用于IHC、WB、 IF、IP、ELISA等科研实验,按理化性质和生物学功能IgM、IgG、IgA、IgE、IgD五类。按抗体的来源,可将其分为天然抗体和**抗体。内皮抑素/内皮他丁抗体生产每个流程都执行严格的检测标准,保证蛋白抗原产物质量,质量稳定,实验效果明显。


内皮抑素/内皮他丁抗体  的详细介绍

内皮抑素/内皮他丁抗体


规格:1尘驳/1尘濒

英文名: Endostatin

别名: Collagen XV alpha 1; Alpha 1 collagen type 18 (XVIII)(COL18A1); Alpha 1 type XVIII collagen; COL18A1; Collagen alpha 1(XVIII) chain; Collagen type XVIII alpha 1; FLJ27325; KNO; MGC74745; COL18A1; COIA

分子量: 20kDa

储存液:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glyce

克隆类型:笔辞濒测肠濒辞苍补濒

亚型:滨驳骋

纯化方法:affinity purified by Protein A

**原:KLH conjugated synthetic peptide derived from human Endostat

交叉反应:Human, Mouse, Rat,

内皮抑素/内皮他丁抗体细胞定位:细胞外基质 分泌型蛋白

产物介绍:background: This gene encodes the alpha chain of type XVIII collagen. This collagen is one of the multiplexins, extracellular matrix proteins that contain multiple triple-helix domains (collagenous domains) interrupted by non-collagenous domains. The proteolytically produced C-terminal fragment of type XVIII collagen is endostatin, a potent antiangiogenic protein. Mutations in this gene are associated with Knobloch syndrome. The main features of this syndrome involve retinal abnormalities so type XVIII collagen may play an important role in retinal structure and in neural tube closure. Two transcript variants encoding different isoforms have been found for this gene. Function: COLA18A probably plays a major内皮抑素/内皮他丁抗体 role in determining the retinal structure as well as in the closure of the neural tube. Endostatin potently inhibits endothelial cell proliferation and angiogenesis. May inhibit angiogenesis by binding to the heparan sulfate proteoglycans involved in growth factor signaling. Subcellular Location: Secreted, extracellular space, extracellular matrix. Tissue Specificity: Present in multiple organs with highest levels in liver, lung and kidney. Post-translational modifications: Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. DISEASE: Defects in COL18A1 are a cause of Knobloch syndrome (KNO) [MIM:267750]. KNO is an autosomal recessive disorder defined by the occurrence of high myopia, vitreoretinal degeneration with retinal detachment, macular abnormalities and occipital encephalocele. Similarity: Belongs to the 内皮抑素/内皮他丁抗体multiplexin collagen family. Contains 1 FZ (frizzled) domain. Contains 1 TSP N-terminal (TSPN) domain. Gene ID: 1306 Database links: Entrez Gene: 1306 Human Entrez Gene: 80781 Human Entrez Gene: 12819 Mouse Entrez Gene: 12822 Mouse Entrez Gene: 85251 Rat Omim: 120328 Human SwissProt: P39059 Human SwissProt: P39060 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 内皮抑素(endostatin)又称胶原蛋白18A1,是目前较理想的血管形成抑制因子,它通过抑制肿瘤血管生成达到阻止肿瘤生长和转移的目的.当前,血管内皮抑制素主要用于抑止肿瘤血管的生长方面的研究。

内皮抑素/内皮他丁抗体产物应用:WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复) not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.

研究领域:肿瘤  **学  生长因子和**  

储存条件: Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

来源: Rabbit

外观: Lyophilized or Liquid


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