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PCSK9 Protein (AA 31-691) (His tag)

PCSK9 宿主: 大鼠 宿主: HEK-293 Cells Recombinant >95 % as determined by reduced SDS-PAGE. Active
产品编号 ABIN2181592
发货至: 中国
  • 抗原 See all PCSK9 蛋白
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    蛋白类型
    Recombinant
    生物活性
    Active
    产品特性
    AA 31-691
    宿主
    • 19
    • 11
    • 6
    • 3
    • 2
    • 2
    • 1
    • 1
    大鼠
    资源
    • 25
    • 7
    • 6
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This PCSK9 protein is labelled with His tag.
    序列
    AA 31-691
    产品特性
    This protein carries a polyhistidine tag at the C-terminus. The protein has a calculated MW of 73.2 kDa. The protein migrates as 22 and 66 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.
    纯度
    >95 % as determined by reduced SDS-PAGE.
    过滤
    0.22 μm filtered
    内毒素水平
    Less than 1.0 EU per μg by the LAL method.
    Top Product
    Discover our top product PCSK9 蛋白
  • 限制
    仅限研究用
  • 状态
    Lyophilized
    缓冲液
    50 mM Tris, 150 mM NaCl, pH 7.5
    注意事项
    Please avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    No activity loss was observed after storage at: In lyophilized state for 1 year (4 °C), After reconstitution under sterile conditions for 3 months (-70 °C).
  • 抗原
    PCSK9 (Proprotein Convertase Subtilisin/kexin Type 9 (PCSK9))
    别名
    PCSK9 (PCSK9 产品)
    别名
    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
    背景
    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).
    分子量
    13.9 kDa and 59.3 kDa
    NCBI登录号
    NP_954862
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