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GIT1 抗体 (AA 415-736)

This 兔 多克隆 antibody specifically detects GIT1 in WB, ELISA, IF, IHC (p) 和 FACS. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN7874885
发货至: 中国
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Quick Overview for GIT1 抗体 (AA 415-736) (ABIN7874885)

抗原

See all GIT1 抗体
GIT1

适用

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人, 大鼠, 小鼠

宿主

  • 116
  • 20

克隆类型

  • 98
  • 38
多克隆

标记

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  • 1
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This GIT1 antibody is un-conjugated

应用范围

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

    • 18
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    • 2
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    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
    AA 415-736

    原理

    GIT1 Antibody / p95-APP1

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids D415-Q736) was used as the immunogen for the GIT1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the GIT1 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 GIT1 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

    GIT1

    别名

    GIT1

    背景

    ARF GTPase-activating protein GIT1 is an enzyme that in humans is encoded by the GIT1 gene. G-protein coupled receptor (GPCR) kinase interacting proteins 1 and 2 (GIT-1 and GIT-2) are highly conserved, ubiquitous scaffold proteins involved in localized signaling to help regulate focal contact assembly and cytoskeletal dynamics. GIT proteins contain multiple interaction domains that allow interaction with small GTPases (including ARF, Rac and cdc42), kinases (such as PAK and MEK), the Rho family GEF PIX, and the focal adhesion protein paxillin. GIT-1 is localized to focal adhesions, cytoplasmic complexes and membrane protrusions, and regulates cell protrusion formation and cell migration. GIT-1 has also been implicated in neuronal functions including synapse formation and the pathology of Huntington disease. Huntington disease is a genetic neurodegenerative condition involving a mutation in the huntington gene. The huntington gene product (htt) is ubiquitinated and degraded in human Huntington disease brains. Htt interacts directly with GIT-1 causing enhanced htt proteolysis, indicating that GIT-1 distribution and function may contribute to Huntington disease pathology.

    UniProt

    Q9Y2X7
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