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OCRL 抗体 (AA 1-901)

The 兔 多克隆 anti-OCRL antibody is suitable to detect OCRL in samples from 人. It has been validated for WB, ELISA, IHC (p) 和 IF.
产品编号 ABIN7869609
发货至: 中国
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Quick Overview for OCRL 抗体 (AA 1-901) (ABIN7869609)

抗原

See all OCRL 抗体
OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

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 OCRL antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • 抗原表位

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    AA 1-901

    原理

    OCRL-1 Antibody

    纯化方法

    Antigen affinity purified

    免疫原

    E. coli-derived recombinant human protein (amino acids M1-D901) was used as the immunogen for the OCRL-1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the OCRL-1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the OCRL-1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    OCRL (Oculocerebrorenal Syndrome of Lowe (OCRL))

    别名

    OCRL-1

    背景

    Inositol polyphosphate 5-phosphatase OCRL-1, also known as Lowe oculocerebrorenal syndrome protein, is an enzyme encoded by the OCRL gene located on the X chromosome in humans. This gene encodes an inositol polyphosphate 5-phosphatase. This protein is involved in regulating membrane trafficking and is located in numerous subcellular locations including the trans-Golgi network, clathrin-coated vesicles and endosomes and the plasma membrane. This protein may also play a role in primary cilium formation. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. Alternate splicing results in multiple transcript variants.

    UniProt

    Q01968

    途径

    Inositol Metabolic Process
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