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Filamin A 抗体 (AA 1725-1775)

This 兔 多克隆 antibody specifically detects Filamin A in IHC 和 IF (p). It exhibits reactivity toward 人.
产品编号 ABIN7448965
发货至: 中国
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北京 101111
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Room 801-803
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Quick Overview for Filamin A 抗体 (AA 1725-1775) (ABIN7448965)

抗原

See all Filamin A (FLNA) 抗体
Filamin A (FLNA) (Filamin A, alpha (FLNA))

适用

  • 115
  • 42
  • 31
  • 3
  • 2
  • 1

宿主

  • 106
  • 9
  • 1

克隆类型

  • 84
  • 32
多克隆

标记

  • 48
  • 8
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  • 2
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  • 2
  • 2
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  • 2
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  • 1
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This Filamin A antibody is un-conjugated

应用范围

  • 65
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  • 28
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  • 25
  • 23
  • 17
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  • 11
  • 7
  • 3
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Immunohistochemistry (IHC), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 15
    • 15
    • 13
    • 6
    • 5
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1725-1775

    原理

    Rabbit anti-Filamin A IHC Antibody, Affinity Purified

    预测反应

    Mouse,Orangutan,Monkey,Gorilla,Dusky titi monkey,White-tufted-ear marmoset,Olive baboon,Northern white-cheeked gibbon,Crab-eating macaque

    纯化方法

    Affinity Purified

    免疫原

    Between AA 1725 and 1775

    亚型

    IgG
  • 应用备注

    IHC-IF: 1:50 - 1:500

    IHC: 1:100 - 1:500

    限制

    仅限研究用
  • 浓度

    50 μg/mL

    缓冲液

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C

    有效期

    12 months
  • 抗原

    Filamin A (FLNA) (Filamin A, alpha (FLNA))

    别名

    Filamin A

    背景

    Background: Filamin A is an actin-binding protein that crosslinks and promotes orthogonal branching of actin filaments and also functions to anchor transmembrane proteins and intracellular signaling proteins to the actin cytoskeleton. As a scaffolding protein, filamin A is able to act as a link between cell membrane receptors and intracellular signaling proteins. Defects in filamin A are associated with multiple human diseases characterized by abnormalities in bone and neurological development.

    基因ID

    2316

    NCBI登录号

    NP_001447

    UniProt

    P21333

    途径

    TCR Signaling, Maintenance of Protein Location
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