Recombinant人SUMF1 protein (ab115708)

概述

描述

  • 性质Recombinant
  • 来源Escherichia coli
  • 氨基酸序列
    • AccessionQ8NBK3
    • 种属Human
    • 序列MGSSHHHHHHSSGLVPRGSHMVPIPAGVFTMGTDDPQIKQDGEAPARRVT IDAFYMDAYEVSNTEFEKFVNSTGYLTEAEKFGDSFVFEGMLSEQVKTNI QQAVAAAPWWLPVKGANWRHPEGPDSTILHRPDHPVLHVSWNDAVAYCTW AGKRLPTEAEWEYSCRGGLHNRLFPWGNKLQPKGQHYANIWQGEFPVTNT GEDGFQGTAPVDAFPPNGYGLYNIVGNAWEWTSDWWTVHHSVEETLNPKG PPSGKDRVKKGGSYMCHRSYCYRYRCAARSQNTPDSSASNLGFRCAADRL PTMD
    • 分子量34 kDa including tags
    • 氨基酸91 to 374
    • 标签His tag N-Terminus

技术指标

Our Abpromise guarantee covers the use of ab115708 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • 应用

    SDS-PAGE

  • 纯度> 85 % SDS-PAGE.

  • 形式Liquid
  • Concentration information loading...

制备和贮存

  • 稳定性和存储

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.32% Tris HCl, 20% Glycerol, 0.03% DTT, 12.01% Urea

常规信息

  • 别名
    • MGC150436
    • AAPA3037
    • C alpha formylglycine generating enzyme 1
    • C-alpha-formylglycine-generating enzyme 1
    • FGE
    • FGly generating enzyme
    • MGC131853
    • Sulfatase modifying factor 1 [Precursor]
    • Sulfatase-modifying factor 1
    • SUMF1
    • SUMF1_HUMAN
    • UNQ3037
    see all
  • 功能Using molecular oxygen and an unidentified reducing agent, oxidizes a cysteine residue in the substrate sulfatase to an active site 3-oxoalanine residue, which is also called C(alpha)-formylglycine. Known substrates include GALNS, ARSA, STS and ARSE.
  • 组织特异性Ubiquitous. Highly expressed in kidney, pancreas and liver. Detected at lower levels in leukocytes, lung, placenta, small intestine, skeletal muscle and heart.
  • 通路Protein modification; sulfatase oxidation.
  • 疾病相关Defects in SUMF1 are the cause of multiple sulfatase deficiency (MSD) [MIM:272200]. MSD is a clinically and biochemically heterogeneous disorder caused by the simultaneous impairment of all sulfatases, due to defective post-translational modification and activation. It combines features of individual sulfatase deficiencies such as metachromatic leukodystrophy, mucopolysaccharidosis, chondrodysplasia punctata, hydrocephalus, ichthyosis, neurologic deterioration and developmental delay. Inheritance is autosomal recessive.
  • 序列相似性Belongs to the sulfatase-modifying factor family.
  • 翻译后修饰N-glycosylated. Contains high-mannose-type oligosaccharides.
  • 细胞定位Endoplasmic reticulum lumen.
  • Information by UniProt

Recombinant Human SUMF1 protein 图像

  • 15% SDS-PAGE showing ab115708 at approximately 34.1kDa (3µg).

Recombinant Human SUMF1 protein (ab115708)参考文献

ab115708 has not yet been referenced specifically in any publications.

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