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Fukutin 抗体 (C-Term)

The 兔 多克隆 anti-Fukutin antibody (ABIN2782105) specifically detects Fukutin in WB. The antibody is reactive with 人, 小鼠, 大鼠, 犬, 马, 兔, 豚鼠, Cow 和 斑马鱼 samples.
产品编号 ABIN2782105
发货至: 中国
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Quick Overview for Fukutin 抗体 (C-Term) (ABIN2782105)

抗原

See all Fukutin (FKTN) 抗体
Fukutin (FKTN)

适用

  • 48
  • 33
  • 17
  • 5
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  • 3
  • 3
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  • 2
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  • 1
人, 小鼠, 大鼠, 犬, 马, 兔, 豚鼠, Cow, 斑马鱼

宿主

  • 48
  • 1

克隆类型

  • 37
  • 12
多克隆

标记

  • 25
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
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  • 2
  • 1
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This Fukutin antibody is un-conjugated

应用范围

  • 39
  • 26
  • 16
  • 6
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 8
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
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    C-Term

    序列

    FGKVEDSLEL SFQGKDDVKL DVFFFYEETD HMWNGGTQAK TGKKFKYLFP

    预测反应

    Cow: 100%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 93%, Rabbit: 100%, Rat: 100%, Zebrafish: 86%

    产品特性

    This is a rabbit polyclonal antibody against FKTN. It was validated on Western Blot.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the C-terminal region of human FKTN
  • 限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    注意事项

    Avoid repeat freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    Fukutin (FKTN)

    别名

    FKTN

    背景

    The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.
    Alias Symbols: FCMD, CMD1X, LGMD2M, MDDGA4, MDDGB4, MDDGC4
    Protein Size: 329

    分子量

    36 kDa

    基因ID

    2218

    NCBI登录号

    NM_001079802, NP_001073270

    UniProt

    O75072

    途径

    Regulation of Carbohydrate Metabolic Process
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