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

PCSK9 Origin: Human Host: HEK-293 Cells Recombinant >90 % as determined by SDS-PAGE. Active
Catalog No. ABIN6388267
  • Target See all PCSK9 Proteins
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    Protein Type
    Recombinant
    Biological Activity
    Active
    Protein Characteristics
    AA 31-692
    Origin
    • 18
    • 11
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    Human
    Source
    • 25
    • 7
    • 6
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This PCSK9 protein is labelled with Fc Tag.
    Sequence
    AA 31-692
    Purity
    >90 % as determined by SDS-PAGE.
    Endotoxin Level
    Less than 1.0 EU per μg by the LAL method.
    Top Product
    Discover our top product PCSK9 Protein
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Buffer
    PBS,  pH 7.4
    Handling Advice
    Please avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
  • Target
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    Alternative Name
    PCSK9 (PCSK9 Products)
    Synonyms
    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
    Background
    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).
    Molecular Weight
    13.8 kDa and 83.7 kDa
    NCBI Accession
    NP_777596
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