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TSPAN13 抗体 (AbBy Fluor® 594)

This anti-TSPAN13 antibody (ABIN2809026) is a Rabbit Polyclonal antibody detecting TSPAN13 in IF (p). Suitable for Human, Mouse, Rat.
产品编号 ABIN2809026
发货至: 中国

Quick Overview for TSPAN13 抗体 (AbBy Fluor® 594) (ABIN2809026)

抗原

See all TSPAN13 抗体
TSPAN13 (Tetraspanin 13 (TSPAN13))

适用

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人, 小鼠, 大鼠

宿主

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克隆类型

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多克隆

标记

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This TSPAN13 antibody is conjugated to AbBy Fluor® 594

应用范围

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Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human TSPAN13/NET-6

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    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

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    TSPAN13 (Tetraspanin 13 (TSPAN13))

    别名

    TSPAN13

    背景

    Synonyms: NET 6, NET6, Tetraspan NET-6, Tetraspanin-13, TM4SF13, Transmembrane 4 superfamily member 13, Transmembrane 4 superfamily member tetraspan NET 6, Tspan-13, Tspan13, TSN13_HUMAN.

    Background: NET-6, also known as TSPAN13 (tetraspanin-13) or TM4SF13 (transmembrane 4 superfamily member 13), is a 204 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. Members of the tetraspanin family are cell-surface proteins that are characterized by the presence of four hydrophobic domains and mediate signal transduction events that play a role in the regulation of cell development, activation, growth, motility, differentiation, and cancer. Considered molecular facilitators, tetraspanin proteins may regulate vesicle fusion and fission. The gene encoding NET-6 maps to human chromosome 7, which houses over 1,000 genes, comprises nearly 5 % of the human genome and has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.

    基因ID

    27075
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