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MCFD2 Protein (Myc-DYKDDDDK Tag)

MCFD2 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2725609
发货至: 中国
  • 抗原 See all MCFD2 蛋白
    MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))
    蛋白类型
    Recombinant
    宿主
    • 3
    • 1
    • 1
    资源
    • 3
    • 1
    • 1
    HEK-293 Cells
    标记
    This MCFD2 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human MCFD2 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MCFD2 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    MCFD2 (Multiple Coagulation Factor Deficiency 2 (MCFD2))
    别名
    Mcfd2 (MCFD2 产品)
    别名
    hm:zeh1186 Protein, wu:fc23b10 Protein, wu:fd50d08 Protein, zgc:103713 Protein, zgc:109915 Protein, MCFD2 Protein, DKFZp469B098 Protein, F5F8D Protein, F5F8D2 Protein, LMAN1IP Protein, SDNSF Protein, 1810021C21Rik Protein, F5f8d Protein, Lman1ip Protein, Sdnsf Protein, multiple coagulation factor deficiency 2 Protein, multiple coagulation factor deficiency 2 L homeolog Protein, MCFD2 Protein, mcfd2 Protein, mcfd2.L Protein, Mcfd2 Protein
    背景
    This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1 also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D) a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
    分子量
    13.5 kDa
    NCBI登录号
    NP_644808
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