Recombinant人MMAB protein (ab99217)

概述

  • 产品名称Recombinant人MMAB protein
  • 蛋白长度Full length protein

描述

  • 性质Recombinant
  • 来源Escherichia coli
  • 氨基酸序列
    • AccessionQ96EY8
    • 种属Human
    • 序列MGSSHHHHHHSSGLVPRGSHMQSRGPQGVEDGDRPQPSSKTPRIPKIYTK TGDKGFSSTFTGERRPKDDQVFEAVGTTDELSSAIGFALELVTEKGHTFA EELQKIQCTLQDVGSALATPCSSAREAHLKYTTFKAGPILELEQWIDKYT SQLPPLTAFILPSGGKISSALHFCRAVCRRAERRVVPLVQMGETDANVAK FLNRLSDYLFTLARYAAMKEGNQEKIYKKNDPSAESEGL
    • 分子量26 kDa including tags
    • 氨基酸33 to 250
    • 标签His tag N-Terminus

技术指标

Our Abpromise guarantee covers the use of ab99217 in the following tested applications.

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

  • 应用

    Mass Spectrometry

    SDS-PAGE

  • 质谱法
    MALDI-TOF
  • 纯度> 95 % SDS-PAGE.
    ab99217 was purified using conventional chromatography techniques.
  • 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.

    Preservative: None
    Constituents: 10% Glycerol, 20mM Tris HCl, pH 7.5

常规信息

  • 别名
    • aquocob(I)alamin vitamin B12s adenosyltransferase
    • ATP:cob(I)alamin adenosyltransferase
    • ATP:corrinoid adenosyltransferase
    • ATR
    • c-diamide adenosyltransferase
    • cblB
    • Cob
    • Cob(I)alamin adenosyltransferase
    • Cob(I)yrinic acid a
    • cob(I)yrinic acid a c diamide adenosyltransferase mitochondrial
    • Methylmalonic aciduria (cobalamin deficiency) cblB type
    • Methylmalonic aciduria type B protein
    • MGC20496
    • mitochondrial
    • MMAB
    • MMAB gene
    • MMAB_HUMAN
    • OTTHUMP00000240563
    • OTTHUMP00000240564
    see all
  • 组织特异性Expressed in liver and skeletal muscle.
  • 通路Cofactor biosynthesis; adenosylcobalamin biosynthesis; adenosylcobalamin from cob(II)yrinate a,c-diamide: step 2/7.
  • 疾病相关Defects in MMAB are the cause of methylmalonic aciduria type cblB (MMAB) [MIM:251110]; also known as methylmalonic aciduria type B or vitamin B12-responsive methylmalonicaciduria of cblB complementation type. MMAB is a disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. Inheritance is autosomal recessive.
  • 序列相似性Belongs to the Cob(I)alamin adenosyltransferase family.
  • 细胞定位Mitochondrion.
  • Information by UniProt

Recombinant Human MMAB protein 图像

  • 15% SDS-PAGE analysis of 3µg ab99217.

Recombinant Human MMAB protein (ab99217)参考文献

ab99217 has not yet been referenced specifically in any publications.

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