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SETBP1 抗体 (AA 501-600) (AbBy Fluor® 594)

This anti-SETBP1 antibody (ABIN2806316) is a Rabbit Polyclonal antibody detecting SETBP1 in IF (cc), IF (p). Suitable for Mouse.
产品编号 ABIN2806316
发货至: 中国

Quick Overview for SETBP1 抗体 (AA 501-600) (AbBy Fluor® 594) (ABIN2806316)

抗原

See all SETBP1 抗体
SETBP1 (SET Binding Protein 1 (SETBP1))

适用

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小鼠

宿主

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克隆类型

  • 27
多克隆

标记

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This SETBP1 antibody is conjugated to AbBy Fluor® 594

应用范围

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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 1
    • 1
    • 1
    AA 501-600

    交叉反应

    小鼠

    预测反应

    Human,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human SETBP1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 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

    SETBP1 (SET Binding Protein 1 (SETBP1))

    别名

    SETBP1

    背景

    Synonyms: SEB, MRD29, SET-binding protein, SETBP1, KIAA0437

    Background: SETBP1 (SET binding protein 1), also known as SEB, is a 1,542 amino acid nuclear protein that contains three AT hook DNA-binding domains, one SKI homology region and a C-terminal SET-binding domain, which is followed by three PPLPPPPP repeats. SETBP1 may be involved in SET-related tumorigenesis and leukemogenesis by regulating the transforming activity of SKI in the nucleus or suppressing SET function. As a widely expressed protein, SETBP1 is encoded by a gene that maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

    基因ID

    26040

    UniProt

    Q9Y6X0
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