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IDS Protein (His tag)

IDS 宿主: 人 宿主: HEK-293 Cells Recombinant > 87 % as determined by reducing SDS-PAGE. Active
产品编号 ABIN7317906
发货至: 中国
  • 抗原 See all IDS 蛋白
    IDS (Iduronate 2-Sulfatase (IDS))
    蛋白类型
    Recombinant
    生物活性
    Active
    宿主
    • 7
    • 3
    • 1
    资源
    • 4
    • 3
    • 2
    • 1
    • 1
    HEK-293 Cells
    标记
    This IDS protein is labelled with His tag.
    原理
    Recombinant Human Iduronate 2-Sulfatase/IDS Protein (His Tag)(Active)
    序列
    Met 1-Pro 550
    产品特性
    A DNA sequence encoding human IDS precursor (NP_000193.1) (Met 1-Pro 550) was expressed with a C-terminal polyhistidine tag.
    纯度
    > 87 % as determined by reducing SDS-PAGE.
    内毒素水平
    < 1.0 EU per μg as determined by the LAL method.
    Biological Activity Comment
    Measured by its ability to hydrolyze the substrate 4-Nitrocatechol Sulfate (PNCS).The specific activity is > 1.0 pmoles/min/μg.
    Top Product
    Discover our top product IDS 蛋白
  • 限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Please refer to the printed manual for detailed information.
    缓冲液
    Lyophilized from sterile PBS, pH 7.4
    储存条件
    4 °C,-20 °C,-80 °C
    储存方法
    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.
  • 抗原
    IDS (Iduronate 2-Sulfatase (IDS))
    别名
    Iduronate 2-Sulfatase/IDS (IDS 产品)
    别名
    mps2 Protein, sids Protein, zgc:158245 Protein, MPS2 Protein, SIDS Protein, AW214631 Protein, iduronate 2-sulfatase Protein, IDS Protein, CpipJ_CPIJ004938 Protein, ids Protein, Ids Protein
    背景

    Background: Iduronate 2-Sulfatase, also known as IDS, is a member of the highly conserved sulfatase family of enzymes that catalyze the hydrolysis of O- and N-sulfate esters from a variety of substrates. The human Iduronate 2-Sulfatase/IDS consists of a signal peptide, a pro peptide and a mature chain that may be further processed into two chains. Among the identified 18 human sulfatases, Iduronate 2-Sulfatase/IDS is required for the lysosomal degradation of the glycosaminoglycans (GAG), heparan sulfate and dermatan sulfate. Multiple mutations in this X-chromosome localized gene result in Iduronate 2-Sulfatase/IDS enzymatic deficiency, and lead to the sex-linked Mucopolysaccharidosis Type II (MPS II ), also known as Hunter Syndrome characterized by the lysosomal accumulation of the GAG and their excretion in urine. MPS II has a wide spectrum of clinical manifestations ranging from mild to severe due to the level of Iduronate 2-Sulfatase/IDS enzyme. Retroviral-mediated Iduronate 2-Sulfatase/IDS gene transfer into lymphoid cells would be a promising gene therapeutic strategy.

    Synonym: IDS,MPS2,SIDS

    分子量
    61 kDa
    NCBI登录号
    NP_000193
    途径
    Glycosaminoglycan Metabolic Process
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