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PKD1 Polyclonal Antibody

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

货号:E-AB-15660

宿主: Rabbit

反应性: H,M

应用: IHC

  • 详情
  • Overview

    Synonyms Autosomal dominant polycystic kidney disease 1 protein,Autosomal dominant polycystic kidney disease protein 1,nPKC-D1,nPKC-mu,OTTHUMP00000208669,OTTHUMP00000208670,PBP,Pc-1,PKD,Pkd1,PKD1,Polycystic Kidney Disease 1,polycystic kidney disease-associated protein,Polycystin 1 Precursor,Polycystin-1,Protein kinase C mu type,Protein kinase D,Serine/threonine-protein kinase D1,transient receptor potential cation channel,subfamily P,member 1,TRPP1,PKD1抗体
    Swissprot P98161
    Source Rabbit
    Reactivity Human,Mouse
    Immunogen Synthetic peptide of human PKD1
    Application IHC(Detection kit: E-IR-R213)
    Recommended dilution IHC,,1:50-1:200
    Concentration 0.6 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Membrane.
    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 encodes a member of the polycystin protein family.The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail.It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis.It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways.It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1).
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