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Gelsolin 抗体 (full length)

The 小鼠 单克隆 anti-Gelsolin antibody (Clone CPTC-Gelsolin-1) (ABIN7878274) specifically detects Gelsolin in WB. The antibody is reactive with 人 samples.
产品编号 ABIN7878274
发货至: 中国
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Quick Overview for Gelsolin 抗体 (full length) (ABIN7878274)

抗原

See all Gelsolin (GSN) 抗体
Gelsolin (GSN)

适用

  • 131
  • 43
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  • 11
  • 7
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  • 2
  • 2
  • 2
  • 1
  • 1
  • 1

宿主

  • 104
  • 34
  • 4
  • 2
小鼠

克隆类型

  • 83
  • 61
单克隆

标记

  • 84
  • 11
  • 5
  • 4
  • 4
  • 4
  • 4
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  • 4
  • 2
  • 2
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  • 1
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  • 1
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  • 1
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This Gelsolin antibody is un-conjugated

应用范围

  • 108
  • 54
  • 40
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  • 19
  • 14
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  • 5
  • 3
  • 2
  • 1
Western Blotting (WB)

质量等级

Carrier-free

克隆位点

CPTC-Gelsolin-1
  • 抗原表位

    • 16
    • 9
    • 5
    • 5
    • 5
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    full length

    原理

    Gelsolin Antibody / GSN (azide and preservative free)

    纯化方法

    Protein G affinity chromatography

    免疫原

    Recombinant human full-length protein was used as the immunogen for this Gelsolin antibody.

    亚型

    IgG1, kappa
  • 应用备注

    Optimal dilution of the Gelsolin antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    4 °C,-20 °C

    储存方法

    Store the Gelsolin antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • 抗原

    Gelsolin (GSN)

    别名

    Gelsolin

    背景

    Gelsolin (also known as brevin, Actin-depolymerizing factor or ADF), a proteinof leukocytes, platelets and other cells, severs Actin filaments in thepresence of submicromolar calcium, thereby isolating cytoplasmic Actin gels. It is a calcium-regulated, actin-modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. Plays a role in ciliogenesis. Defects in GSN are the cause of amyloidosis type 5 (AMYL5), also known as familial amyloidosis Finnish type, typically characterized by cranial neuropathy and lattice corneal dystrophy. Severe systemic disease can develop in some individuals causing peripheral polyneuropathy, amyloid cardiomyopathy, and nephrotic syndrome leading to renal failure.

    UniProt

    P06396

    途径

    Caspase Cascade in Apoptosis, Regulation of Actin Filament Polymerization, Autophagy
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