IκB-α (Phospho Ser36) Rabbit mAb

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¥880.00

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产品规格:
  • 50μL
货号:

FAB2621824

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商品描述
  • 靶点-Target

    IκB-α

  • 反应性

    Human,Mouse,Rat

  • 应用

    WB,IHC,IF,ELISA

  • 宿主物种-Host Species

    Rabbit

  • 同种型-Isotype

    IgG,Kappa

  • 偶联-Conjugate

    Phospho

  • 修饰-Modification

    Ser36

  • MW(Calculated)

    36kD

  • MW(Observed)

    39kD

  • 推荐稀释比

    IHC 1:500-1:1000;WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;

  • 组成

    PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

  • 纯化工艺

    Protein A

  • 储存

    -15°C to -25°C/1 year(Do not lower than -25°C)

  • 克隆性

    Monoclonal

  • 克隆号

    PT1061R

  • 特异性

    IκB-α (Phospho Ser36) Monoclonal Antibody detects endogenous levels of IκB-α only when phosphorylated at Ser36.and dually phosphorylated at two sites.The name of modified sites may be influenced by many factors, such as species (the modified site was not originally found in human samples) and the change of protein sequence (the previous protein sequence is incomplete, and the protein sequence may be prolonged with the development of protein sequencing technology). When naming, we will use the "numbers" in historical reference to keep the sites consistent with the reports. The antibody binds to the following modification sequence (lowercase letters are modification sites):LDsMK

  • 基因名称

    NFKBIA IKBA MAD3 NFKBI

  • 蛋白名称

    NF-kappa-B inhibitor alpha

  • 别名

    NFKBIA;IKBA;MAD3;NFKBI;NF-kappa-B inhibitor alpha;I-kappa-B-alpha;IkB-alpha;IkappaBalpha;Major histocompatibility complex enhancer-binding protein MAD3

  • Organism-1

    Human

  • 基因ID-1

    4792

  • SwissProt-1

    P25963

  • Organism-2

    Mouse

  • 基因ID-2

    18035

  • SwissProt-2

    Q9Z1E3

  • Organism-3

    Rat

  • 基因ID-3

    25493

  • SwissProt-3

    Q63746

  • 背景

    This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease. [provided by RefSeq, Aug 2011],

  • 细胞定位

    Cytoplasm. Nucleus. Shuttles between the nucleus and the cytoplasm by a nuclear localization signal (NLS) and a CRM1-dependent nuclear export. .