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Dynactin 1 抗体 (AA 1042-1278)

This 兔 多克隆 antibody specifically detects Dynactin 1 in WB, ELISA, IF, IHC (p) 和 FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7869971
发货至: 中国
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Quick Overview for Dynactin 1 抗体 (AA 1042-1278) (ABIN7869971)

抗原

See all Dynactin 1 (DCTN1) 抗体
Dynactin 1 (DCTN1)

适用

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  • 1
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人, 小鼠, 大鼠

宿主

  • 40
  • 13
  • 1
  • 1

克隆类型

  • 41
  • 14
多克隆

标记

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This Dynactin 1 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

    • 15
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1042-1278

    原理

    DCTN1 Antibody / p150-glued / Dynactin

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids K1042-S1278) was used as the immunogen for the DCTN1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the DCTN1 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 DCTN1 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

    Dynactin 1 (DCTN1)

    别名

    DCTN1

    背景

    Dynactin subunit 1 is a protein that in humans is encoded by the DCTN1 gene. This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 10 subunits ranging in size from 22 to 150 kD. Dynactin binds to both microtubules and cytoplasmic dynein. Dynactin is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis. This subunit interacts with dynein intermediate chain by its domains directly binding to dynein and binds to microtubules via a highly conserved glycine-rich cytoskeleton-associated protein (CAP-Gly) domain in its N-terminus. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause distal hereditary motor neuronopathy type VIIB (HMN7B) which is also known as distal spinal and bulbar muscular atrophy (dSBMA).

    UniProt

    Q14203

    途径

    M Phase, ER-Nucleus Signaling
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