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产品中心-北京博奥森生物技术有限公司
Recombinant mouse TMEM158 protein, N-His (bs-42089P)  
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20ug/580.00元
100ug/1880.00元
500ug/5680.00元
大包装/询价

产品编号 bs-42089P
英文名称 Recombinant mouse TMEM158 protein, N-His
中文名称 重组小鼠跨膜蛋白158
别    名 40 kDa BINP binding protein; 40 kDa BINP-binding protein; BBP; BINP receptor; Brain injury derived neurotrophic peptide (BINP) binding protein; Brain specific binding protein; DKFZp586E1621; HBBP; p40BBP; Ras induced senescence protein 1; Ras-induced senescence protein 1; RIS1; TM158_HUMAN; TMEM 158; TMEM158; Transmembrane protein 158.  
克 隆 号
理论分子量 25.1 kDa
检测分子量
性    状 Lyophilized or Liquid
浓    度 >1mg/ml
物    种 Mouse
序    列 21-204/286
纯    度 >90% as determined by SDS-PAGE
纯化方法 AC
内毒素 Not analyzed
表达系统 E.coli
活性 Not tested
标签 N-His
缓 冲 液 20mM Tris-HCl (pH8.0)with 1mM DTT.
保存条件 Stored at -70℃ or -20℃. 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 TMEM158 is a 286 amino acid protein encoded by a gene mapping to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

产品图片
The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.
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