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POMT1 抗体

The 兔 多克隆 anti-POMT1 antibody (ABIN2458911) specifically detects POMT1 in WB 和 ELISA. The antibody is reactive with 人 samples.
产品编号 ABIN2458911
发货至: 中国
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Quick Overview for POMT1 抗体 (ABIN2458911)

抗原

See all POMT1 抗体
POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

适用

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宿主

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克隆类型

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多克隆

标记

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This POMT1 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human POMT1.
  • 应用备注

    POMT1 antibody can be used for detection of POMT1 by ELISA at 1:62500. POMT1 antibody can be used for detection of POMT1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store POMT1 antibody at -20 °C.
  • 抗原

    POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

    别名

    POMT1

    背景

    POMT1 is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K).O-mannosylation is an important protein modification in eukaryotes that is initiated by an evolutionarily conserved family of protein O-mannosyltransferases. POMT1 shares sequence similarity with protein O-mannosyltransferases of S. cerevisiae. In yeast, these enzymes are located in the endoplasmic reticulum (ER) and are required for cell integrity and cell wall rigidity. POMT1 also shows similarity to the Drosophila 'rotated abdomen' (rt) gene, which when mutated causes defects in myogenesis and muscle structure.

    分子量

    82 kDa

    基因ID

    10585

    NCBI登录号

    NP_001070833

    UniProt

    B3KQG0
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