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PKD1 antibody

PKD1 Reactivity: Human, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2431381
  • Target See all PKD1 Antibodies
    PKD1 (Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1))
    Reactivity
    • 39
    • 27
    • 10
    • 1
    • 1
    Human, Mouse
    Host
    • 38
    • 1
    Rabbit
    Clonality
    • 39
    Polyclonal
    Conjugate
    • 14
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PKD1 antibody is un-conjugated
    Application
    • 25
    • 17
    • 14
    • 13
    • 13
    • 7
    • 7
    • 3
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human PKD1
    Isotype
    IgG
    Top Product
    Discover our top product PKD1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.6 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    PKD1 (Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1))
    Alternative Name
    PKD1 (PKD1 Products)
    Synonyms
    PBP antibody, Pc-1 antibody, TRPP1 antibody, PC1 antibody, mFLJ00285 antibody, polycystin 1, transient receptor potential channel interacting antibody, polycystin 1, transient receptor poteintial channel interacting antibody, polycystin-1 antibody, PKD1 antibody, Pkd1 antibody, LOC749291 antibody
    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).
    NCBI Accession
    NP_001009944
    Pathways
    Myometrial Relaxation and Contraction, Maintenance of Protein Location
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