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PCSK9 Protein (AA 31-692) (Fc Tag)

PCSK9 Origine: Humain Hôte: HEK-293 Cells Recombinant >90 % as determined by SDS-PAGE. Active
N° du produit ABIN6388267
  • Antigène Voir toutes PCSK9 Protéines
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    Type de proteíne
    Recombinant
    Activité biologique
    Active
    Attributs du protein
    AA 31-692
    Origine
    • 19
    • 11
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    Humain
    Source
    • 25
    • 7
    • 6
    • 2
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette PCSK9 protéine est marqué à la Fc Tag.
    Séquence
    AA 31-692
    Pureté
    >90 % as determined by SDS-PAGE.
    niveau d'endotoxine
    Less than 1.0 EU per μg by the LAL method.
    Top Product
    Discover our top product PCSK9 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    PBS,  pH 7.4
    Conseil sur la manipulation
    Please avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
  • Antigène
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    Autre désignation
    PCSK9 (PCSK9 Produits)
    Synonymes
    FH3 Protein, HCHOLA3 Protein, LDLCQ1 Protein, NARC-1 Protein, NARC1 Protein, PC9 Protein, AI415265 Protein, AI747682 Protein, Narc1 Protein, proprotein convertase subtilisin/kexin type 9 Protein, proprotein convertase subtilisin/kexin type 9 L homeolog Protein, PCSK9 Protein, pcsk9.L Protein, pcsk9 Protein, Pcsk9 Protein
    Sujet
    Proprotein convertase subtilisin/kexin type 9 (PCSK9), is an enzyme which in humans is encoded by the PCSK9 gene. This gene encodes a proprotein convertase belonging to the proteinase K subfamily of the secretory subtilase family. This protein plays a major regulatory role in cholesterol homeostasis. PCSK9 binds to the epidermal growth factor-like repeat A (EGF-A) domain of the low-density lipoprotein receptor (LDLR), inducing LDLR degradation. PCSK9 may also have a role in the differentiation of cortical neurons. Mutations in this gene have been associated with a rare form of autosomal dominant familial hypercholesterolemia (HCHOLA3).
    Poids moléculaire
    13.8 kDa and 83.7 kDa
    NCBI Accession
    NP_777596
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