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SMAD4 Polyclonal Antibody

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

货号:E-AB-70073

宿主: Rabbit

反应性: H,M

应用: WB

  • 详情
  • Overview

    Synonyms (Small) Mothers Against Decapentaplegic,Deleted in Pancreatic Carcinoma 4,Deleted in Pancreatic Carcinoma,Deleted in pancreatic carcinoma locus 4,Deletion target in pancreatic carcinoma 4,DPC 4,DPC4,hSMAD4,JIP,MAD homolog 4,MAD mothers against decapentaplegic Drosophila homolog 4,MAD mothers against decapentaplegic homolog 4,MADH 4,MADH4,Med,Medea,Mothers against decapentaplegic homolog 4,Mothers against decapentaplegic,Drosophila,homolog of,4,Mothers against DPP homolog 4,MYHRS,OTTHUMP00000163548,SMA- and MAD-related protein 4,SMAD 4,SMAD family member 4,SMAD mothers against DPP homolog 4,SMAD4,SMAD4,SMAD4抗体
    Swissprot Q13485,P97471,O70437
    Source Rabbit
    Reactivity Human,Mouse
    Immunogen KLH conjugated Synthetic peptide corresponding to Mouse Smad4
    Application WB(Detection kit: E-IR-R304)
    Recommended dilution WB,,1:500-1:2000;
    Concentration 0.62 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytoplasm, Nucleus
    Tissue specificity Highest expression level in kidney
    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 member of the Smad family of signal transduction proteins. Smad proteins are phosphorylated and activated by transmembrane serine-threonine receptor kinases in response to TGF-beta signaling. The product of this gene forms homomeric complexes and heteromeric complexes with other activated Smad proteins, which then accumulate in the nucleus and regulate the transcription of target genes. This protein binds to DNA and recognizes an 8-bp palindromic sequence (GTCTAGAC) called the Smad-binding element (SBE). The Smad proteins are subject to complex regulation by post-translational modifications. Mutations or deletions in this gene have been shown to result in pancreatic cancer, juvenile polyposis syndrome, and hereditary hemorrhagic telangiectasia syndrome. SMAD4 (SMAD Family Member 4) is a Protein Coding gene. Diseases associated with SMAD4 include Myhre Syndrome and Polyposis, Juvenile Intestinal. Among its related pathways are PEDF Induced Signaling and Validated targets of C-MYC transcriptional repression. GO annotations related to this gene include transcription factor activity, sequence-specific DNA binding and sequence-specific DNA binding. An important paralog of this gene is SMAD9.
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