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肿瘤血管内皮标记相关蛋白质7抗体

实验类型: WB,IHC-P,IHC-F,ICC,IF,ELISA
检测范围:
最低检测限:
应用范围: (predicted: Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,Rabbit,Sheep)
UniProt NO:
表达区域:

公司产品仅供科研研究实验,不得用于临床!

商品详情:

英文名称:TEM7R

中文名称:肿瘤血管内皮标记相关蛋白质7抗体

    名;Tumor endothelial marker 7 related protein; Plexin domain containing 2; Plexin domain containing protein 2; Plexin domain-containing protein 2; PLXDC 2; plxdc2; PXDC2_HUMAN; TEM7R; Tumor endothelial marker 7-related protein.

研究领域;肿瘤  血管内皮细胞  肿瘤细胞生物标志物

抗体来源;Rabbit

克隆类型;Polyclonal

交叉反应;(predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )

产品应用;WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=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.

理论分子量;56kDa

细胞定位;细胞膜

    状;Liquid

    度;1mg/ml

免 疫 原;KLH conjugated synthetic peptide derived from human TEM7R.: 101-200/529 <Extracellular>

    型;IgG

纯化方法;affinity purified by Protein A

保存条件;Shipped at 4. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

注意事项;This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

产品介绍;TEM7R also known as PLXDC2 is a 529 amino acid single-pass type I membrane protein containing one PSI domain and belonging to the plexin family. Localizing to membrane, TEM7R is expressed in endothelial cells of the stroma, as well as in limbs, lung buds, developing heart, spinal cord and dorsal root ganglia. TEM7R interacts with cortactin and may play a role in tumor angiogenesis. Existing as three alternatively spliced isoforms, the gene encoding TEM7R maps to human chromosome 10p12.31. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolmans syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Function:

May play a role in tumor angiogenesis.

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