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bs-104206P

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  • 2025年10月15日
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      20ug/50ug/100ug

    规格:20ug产品价格:¥980.0
    规格:50ug产品价格:¥1880.0
    规格:100ug产品价格:¥2680.0
    产品编号bs-104206P
    英文名称Recombinant Human MTMR2 Protein, N-His
    英文别名Phosphatidylinositol-3; 5-bisphosphate 3-phosphatase; Phosphatidylinositol-3-phosphate phosphatase; Myotubularin-related protein 2; MTMR2; KIAA1073
    性状Lyophilized
    纯化方法AC
    理论分子量61.06 kDa
    储存液Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
    研究领域

    Neuroscience > Neurology process > Neurodegenerative disease

    Signal Transduction > Protein Phosphorylation > Tyrosine Phosphatases

    亚基Homooligomer and heterooligomer. Interacts with SBF1 and SBF2.
    亚细胞定位Cytoplasm. Membrane. Partly associated with membranes.
    翻译后修饰Phosphorylation at Ser-58 decreases MTMR2 localization to endocytic vesicular structures.
    相似性Belongs to the protein-tyrosine phosphatase family. Non-receptor class myotubularin subfamily.
    Contains 1 GRAM domain.
    Contains 1 myotubularin phosphatase domain.
    功能Phosphatase that acts on lipids with a phosphoinositol headgroup. Has phosphatase activity towards phosphatidylinositol-3-phosphate and phosphatidylinositol-3,5-bisphosphate.
    保存条件Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料Myotubularin and the myotubularin-related proteins (MTMR1-9) belong to a highly conserved family of eukaryotic phosphatases. They are protein tyrosine phosphatases that utilize inositol phospholipids, rather than phosphoproteins, as substrates. MTMR family members hydrolyze both Phosphatidylinositol 3-phosphate (PtdIns3P) and PtdIns(3,5)P2. MTMR2 interacts with MTMR5, an inactive family member that increases the enzymatic activity of MTMR2 and dictates its subcellular localization. Mutations in MTMR2 cause autosomal recessive Charcot-Marie-Tooth type 4B1 (CMT4B1), which is characterized by reduced nerve conduction velocities, focally folded myelin sheaths and demyelination. MTMR3 and MTMR4 can either interact with each other or self associate. MTMR6 regulates the activity of the calcium-activated potassium channel 3.1. MTMR9 regulates the activity of MTMR7 and MTMR8.

     

     

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