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VHLL Protein (AA 1-154) (His tag)

VHLL 宿主: 人 Recombinant > 95.0 % as determined by SDS-PAGE.
产品编号 ABIN620853
发货至: 中国
  • 抗原 See all VHLL 蛋白
    VHLL (Von Hippel-Lindau Tumor Suppressor-Like (VHLL))
    蛋白类型
    Recombinant
    产品特性
    AA 1-154
    宿主
    宿主
    请咨询
    标记
    This VHLL protein is labelled with His tag.
    序列
    MGSSHHHHHH SSGLVPRGSH MPRRAENWDE AEVGAEEAGV EEYGPEEDGG EESGAEESGPEESGPEELGA EEEMEAGRPR PVLRSVNSRE PSQVIFCNRS PRVVLPVWLN FDGEPQPYPT LPPGTGRRIH SYRGHLWLFR DAGTHDGLLV NQTELFVPSL NVDGQPIFAN ITLP.
    产品特性
    Recombinant Human Von Hippel-Lindau Protein
    纯度
    > 95.0 % as determined by SDS-PAGE.
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    Discover our top product VHLL 蛋白
  • 限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    The Von Hippel-Lindau Protein contains 1x PBS pH-7.4, 2mM EDTA, and 1mM DTT.
    储存条件
    4 °C
  • 抗原
    VHLL (Von Hippel-Lindau Tumor Suppressor-Like (VHLL))
    别名
    Von Hippel-Lindau Protein (VHLL 产品)
    背景
    Recombinant Human Von Hippel-Lindau Protein b-domain produced in E. coli is a single, non-glycosylated polypeptide chain containing 174 AA (1-154) and having a molecular mass of 19.2 kDa. The Von Hippel-Lindau antigen is fused to 20 AA His-Tag at N-terminus and purified by proprietary chromatography techniques. Introduction: Von Hippel-Lindau disease is a dominant inherited syndrome characterized by the predisposition to develop various kinds of benign and malignant tumors, including clear cell renal carcinomas, pheochromocytomas and hemangioblastomas of the central nervous system and retina. VHL syndrome is caused by germline mutation in the VHL tumor suppressor, and VHL tumors are associated with loss or mutation of the remaining wild-type allele. VHL has two domains: a roughly 100-residue NH2-terminal domain rich in b sheet (b-domain) and a smaller a-helical domain (a-domain), held together by two linkers and a polar interface. VHL protein is also involved in the degradation of hypoxia-inducible factor (HIF). Synonyms: Von Hippel-Lindau disease tumor suppressor, pVHL, Protein G7, VHL, RCA1, VHL1, HRCA1.
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