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p27 Polyclonal Antibody

规格: / 60μL / 120μL / 200μL
价格: / ¥1380 / ¥2220 / ¥3300

货号:E-AB-70069

宿主: Rabbit

反应性: H,R

应用: IHC

  • 详情
  • 文献(3)
  • Overview

    Synonyms AA408329,AI843786,Cdki1b,CDKN 1B,CDKN 4,CDKN1B,CDKN4,CDN1B,Cyclin Dependent Kinase Inhibitor 1B,Cyclin dependent kinase inhibitor p27,Cyclin-dependent kinase inhibitor 1B (p27,Kip1),Cyclin-dependent kinase inhibitor 1B,Cyclin-dependent kinase inhibitor p27,Cyclin-dependent kinase inhibitor p27 Kip1,KIP 1,KIP1,MEN1B,MEN4,OTTHUMP00000195098,OTTHUMP00000195099,p27,p27 Kip1,P27-like cyclin-dependent kinase inhibitor,p27Kip1,p27抗体
    Swissprot P46527,P46414
    Source Rabbit
    Reactivity Human,Rat
    Immunogen KLH conjugated Synthetic peptide corresponding to Mouse P27 KIP1
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:100-1:400;
    Concentration 0.89 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Nucleus. Cytoplasm. Endosome. Nuclear and cytoplasmic in quiescent cells. AKT-or RSK-mediated phosphorylation on Thr-198, binds 14-3-3, translocates to the cytoplasm and promotes cell cycle progression. Mitogen-activated UHMK1 phosphorylation on Ser-10 also results in translocation to the cytoplasm and cell cycle progression. Phosphorylation on Ser-10 facilitates nuclear export. Translocates to the nucleus on phosphorylation of Tyr-88 and Tyr-89. Colocalizes at the endosome with SNX6 and this leads to lysosomal degradation.
    Tissue specificity Expressed in all tissues tested. Highest levels in skeletal muscle, lowest in liver and kidney.Highest expression level in pigmented layer of retina.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.02% sodium azide,100 μg/ml BSA and 50% glycerol.
    Background This gene encodes a cyclin-dependent kinase inhibitor, which shares a limited similarity with CDK inhibitor CDKN1A/p21. The encoded protein binds to and prevents the activation of cyclin E-CDK2 or cyclin D-CDK4 complexes, and thus controls the cell cycle progression at G1. The degradation of this protein, which is triggered by its CDK dependent phosphorylation and subsequent ubiquitination by SCF complexes, is required for the cellular transition from quiescence to the proliferative state. Mutations in this gene are associated with multiple endocrine neoplasia type IV (MEN4).
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