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Myeloperoxidase Protein (MPO) (His tag)

MPO Origine: Souris Hôte: Human Cells Recombinant > 90 % as determined by reducing SDS-PAGE.
N° du produit ABIN7320799
  • Antigène Voir toutes Myeloperoxidase (MPO) Protéines
    Myeloperoxidase (MPO)
    Type de proteíne
    Recombinant
    Origine
    • 16
    • 7
    • 3
    • 2
    • 2
    • 2
    Souris
    Source
    • 12
    • 8
    • 3
    • 2
    • 2
    • 1
    Human Cells
    Purification/Conjugué
    Cette Myeloperoxidase protéine est marqué à la His tag.
    Fonction
    Recombinant Mouse Myeloperoxidase/MPO Protein (His Tag)
    Séquence
    Met16-Thr718
    Attributs du produit
    Recombinant Mouse Myeloperoxidase is produced by our Mammalian expression system and the target gene encoding Met16-Thr718 is expressed with a 10His tag at the C-terminus.
    Pureté
    > 90 % as determined by reducing SDS-PAGE.
    niveau d'endotoxine
    < 1.0 EU per μg as determined by the LAL method.
    Top Product
    Discover our top product MPO Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Antigène
    Myeloperoxidase (MPO)
    Autre désignation
    Myeloperoxidase/MPO (MPO Produits)
    Synonymes
    mKIAA4033 Protein, MPO Protein, LOC100335032 Protein, POX2' Protein, XPOX2' Protein, mpo Protein, mpo-A Protein, pmr-1 Protein, pmr1 Protein, pox2 Protein, xpox2 Protein, myeloperoxidase Protein, myeloperoxidase L homeolog Protein, MPO Protein, Mpo Protein, LOC100335032 Protein, mpo.L Protein
    Sujet

    Background: Myeloperoxidase (MPO) is a hemecontaining enzyme belonging to the XPO subfamily of peroxidases. It is an abundant neutrophil and monocyte glycoprotein that catalyzes the hydrogen peroxidedependent conversion of chloride, bromide, and iodide to multiple reactive species. MPO activity results in protein nitrosylation and the formation of 3-chlorotyrosine and dityrosine crosslinks. Modification of ApoB100, as well as the lipid and cholesterol components of LDL and HDL, promotes the development of atherosclerosis. MPO is also associated with a variety of other diseases, and inhibits vasodilation in inflammation by depleting the levels of NO. Serum albumin functions as a carrier protein during MPO movement to the basolateral side of epithelial cells. MPO is stored in neutrophil azurophilic granules. Upon cellular activation, it is deposited into pathogencontaining phagosomes. While mice lacking MPO are impaired in clearing select microbial infections,MPO deficiency in humans does not necessarily result in heightened susceptibility to infections.

    Synonym: Myeloperoxidase, MPO

    Poids moléculaire
    81.1 kDa
    UniProt
    P11247
    Pathways
    Chromatin Binding
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