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ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1) Peptide

ATP2C1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN973612
  • Antigène Tous les produits ATP2C1
    ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
    Origine
    Humain
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-ATP2C1 antibody (Catalog #: ARP44399_P050). 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.
    Purification
    Purified
  • Indications d'application
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    ATP2C1 (ATPase, Ca++ Transporting, Type 2C, Member 1 (ATP2C1))
    Synonymes
    ATP2C1 Peptide, ATP2C1A Peptide, BCPM Peptide, HHD Peptide, PMR1 Peptide, SPCA1 Peptide, hSPCA1 Peptide, Spca1 Peptide, si:dkey-11p23.6 Peptide, SPCA Peptide, 1700121J11Rik Peptide, AW061228 Peptide, D930003G21Rik Peptide, pmr1 Peptide, ATPase secretory pathway Ca2+ transporting 1 Peptide, ATPase, Ca++ transporting, type 2C, member 1 Peptide, ATPase, Ca++-sequestering Peptide, ATP2C1 Peptide, atp2c1 Peptide, Atp2c1 Peptide
    Sujet
    ATP2C1 belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.

    Alias Symbols: ATP2C1A, BCPM, HHD, KIAA1347, PMR1, SPCA1, hSPCA1

    Protein Size: 888
    Poids moléculaire
    98 kDa
    ID gène
    27032
    NCBI Accession
    NM_001001485, NP_001001485
    UniProt
    P98194
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