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p16 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-13142

宿主: Rabbit

反应性: H

应用: IHC

  • 详情
  • Overview

    Synonyms CCM2,CDK4 inhibitor p16 INK4,CDK4I,CDKN2,CDKN2A,Cell cycle negative regulator beta,CMM2,Cyclin dependent kinase 4 inhibitor A,Cyclin dependent kinase inhibitor 2A (melanoma p16 inhibits CDK4),Cyclin Dependent Kinase Inhibitor 2A,Cyclin dependent kinase inhibitor 2A isoform 4,Cyclin dependent kinase inhibitor 2A isoforms 1/2/3,Cyclin dependent kinase inhibitor p16,INK4,INK4A,MLM,MTS1,Multiple tumor suppressor 1,p14,p16,P16INK4,p16INK4a,p19,p19Arf,TP16,CDKN2A抗体
    Swissprot P42771
    Source Rabbit
    Reactivity Human
    Immunogen Synthetic peptide of human CDKN2A
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:50-1:200
    Concentration 1 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytoplasmic and Nuclear
    Tissue specificity Widely expressed but not detected in brain or skeletal muscle. Isoform 3 is pancreas-specific.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background This gene generates several transcript variants which differ in their first exons.At least three alternatively spliced variants encoding distinct proteins have been reported, two of which encode structurally related isoforms known to function as inhibitors of CDK4 kinase.The remaining transcript includes an alternate first exon located 20 Kb upstream of the remainder of the gene; this transcript contains an alternate open reading frame (ARF) that specifies a protein which is structurally unrelated to the products of the other variants.This ARF product functions as a stabilizer of the tumor suppressor protein p53 as it can interact with, and sequester, the E3 ubiquitin-protein ligase MDM2, a protein responsible for the degradation of p53.
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