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Inositol Monophosphatase Domain Containing 1 (IMPAD1) (Middle Region) Peptide

IMPAD1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5673273
  • Antigène Tous les produits IMPAD1
    IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 4
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    YVTTMVCVAV NGKPMLGVIH KPFSEYTAWA MVDGGSNVKA RSSYNEKTPR
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- IMPAD1 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
    Synonymes
    IMP 3 Peptide, RGD1306455 Peptide, gPAPP Peptide, impa3 Peptide, 1110001C20Rik Peptide, AA408880 Peptide, AI451589 Peptide, AL022796 Peptide, B230207P20 Peptide, Jaws Peptide, GPAPP Peptide, IMP-3 Peptide, IMPA3 Peptide, IMPase 3 Peptide, zgc:123256 Peptide, inositol monophosphatase domain containing 1 Peptide, inositol monophosphatase domain containing 1 S homeolog Peptide, Impad1 Peptide, impad1.S Peptide, IMPAD1 Peptide, impad1 Peptide
    Sujet
    This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.

    Alias Symbols: GPAPP, IMP 3, IMP-3, IMPA3

    Protein Size: 359
    ID gène
    54928
    NCBI Accession
    NM_017813, NP_060283
    UniProt
    Q9NX62
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