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Dysferlin 抗体 (AA 51-747) (Fluoro647)

The Fluoro647-conjugated 兔 多克隆 anti-Dysferlin antibody (ABIN7986677) specifically detects Dysferlin in FACS. The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN7986677
发货至: 中国
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Quick Overview for Dysferlin 抗体 (AA 51-747) (Fluoro647) (ABIN7986677)

抗原

See all Dysferlin (DYSF) 抗体
Dysferlin (DYSF)

适用

  • 80
  • 46
  • 16
  • 4
  • 4
  • 4
  • 4
  • 2
  • 2
  • 2
  • 2
人, 小鼠, 大鼠

宿主

  • 75
  • 4
  • 1

克隆类型

  • 56
  • 24
多克隆

标记

  • 29
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Dysferlin antibody is conjugated to Fluoro647

应用范围

  • 34
  • 25
  • 24
  • 20
  • 19
  • 15
  • 3
  • 3
  • 2
  • 1
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 16
    • 12
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 51-747

    原理

    Anti-Dysferlin/DYSF Antibody Fluoro647 Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human DYSF recombinant protein (Position: E51-H747).

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    Dysferlin (DYSF)

    别名

    DYSF

    背景

    Background: Dysferlin also known as dystrophy-associated fer-1-like protein is a protein that in humans is encoded by the DYSF gene. The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants.

    Gene Full Name: dysferlin

    基因ID

    8291

    UniProt

    O75923
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