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TTR 抗体

This 兔 多克隆 anti-TTR antibody specifically detects TTR in WB. The antibody is reactive with 人 samples.
产品编号 ABIN2854289
发货至: 中国
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北京 101111
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Beijing Economic Technological Development Area
Room 801-803
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Quick Overview for TTR 抗体 (ABIN2854289)

抗原

See all TTR 抗体
TTR (Transthyretin (TTR))

适用

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宿主

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克隆类型

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多克隆

标记

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This TTR antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 交叉反应

    人, 小鼠, 大鼠

    产品特性

    Rabbit Polyclonal antibody to Transthyretin (transthyretin)
    Transthyretin antibody [N1C3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Full length human Prealbumin Recombinant protein.

    亚型

    IgG
  • 应用备注

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: rat plasma

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.58 mg/mL

    缓冲液

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    储存液

    ProClin

    注意事项

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

    储存条件

    4 °C,-20 °C

    储存方法

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    TTR (Transthyretin (TTR))

    别名

    transthyretin

    背景

    This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein, it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported, most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

    Cellular Localization: Secreted , Cytoplasm

    分子量

    16 kDa

    基因ID

    7276

    UniProt

    P02766

    途径

    Hormone Transport
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