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Fukutin 抗体 (AA 111-160)

This 兔 多克隆 anti-Fukutin antibody specifically detects Fukutin in WB 和 ELISA. The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN7228550
发货至: 中国
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Quick Overview for Fukutin 抗体 (AA 111-160) (ABIN7228550)

抗原

See all Fukutin (FKTN) 抗体
Fukutin (FKTN)

适用

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  • 33
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人, 小鼠

宿主

  • 48
  • 1

克隆类型

  • 37
  • 12
多克隆

标记

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This Fukutin antibody is un-conjugated

应用范围

  • 39
  • 26
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Western Blotting (WB), ELISA
  • 抗原表位

    • 8
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    • 1
    • 1
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    AA 111-160

    原理

    FKTN Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of FKTN protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human FKTN protein at AA range: 111-160

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    Fukutin (FKTN)

    别名

    FKTN

    背景

    Rabbit Anti-FKTN Polyclonal Antibody,Fukutin, Fukuyama-type congenital muscular dystrophy protein,The protein encoded by FKTN 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 FKTN 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 FKTN.,FKTN

    分子量

    observerd band 50kDa

    基因ID

    2218

    UniProt

    O75072

    途径

    Regulation of Carbohydrate Metabolic Process
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