Recombinant人Mimitin protein (ab109967)

概述

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

描述

  • 性质Recombinant
  • 来源Escherichia coli
  • 氨基酸序列
    • AccessionQ8N183
    • 种属Human
    • 序列MGSSHHHHHHSSGLVPRGSHMGWSQDLFRALWRSLSREVKEHVGTDQFGN KYYYIPQYKNWRGQTIREKRIVEAANKKEVDYEAGDIPTEWEAWIRRTRK TPPTMEEILKNEKHREEIKIKSQDFYEKEKLLSKETSEELLPPPVQTQIK GHASAPYFGKEEPSVAPSSTGKTFQPGSWMPRDGKSHNQ
    • 分子量22 kDa including tags
    • 氨基酸1 to 169
    • 标签His tag N-Terminus

技术指标

Our Abpromise guarantee covers the use of ab109967 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

    Mass Spectrometry

  • 质谱法
    MALDI-TOF
  • 纯度> 85 % SDS-PAGE.
    ab109967 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. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

    Preservative: None
    Constituents: 20% Glycerol, 200mM Sodium chloride, 20mM Tris HCl, 1mM DTT, pH 8.0

常规信息

  • 别名
    • B17.2 like
    • B17.2-like
    • B17.2L
    • FLJ22398
    • MIMIT_HUMAN
    • Mimitin
    • Mimitin mitochondrial
    • mitochondrial
    • MMTN
    • Myc induced mitochondrial protein
    • Myc-induced mitochondrial protein
    • NADH dehydrogenase (ubiquinone) 1 alpha subcomplex assembly factor 2
    • NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
    • NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2
    • NDUFA12 like
    • NDUFA12 like protein
    • NDUFA12-like protein
    • NDUFA12L
    • NDUFAF2
    • OTTHUMP00000161882
    • OTTHUMP00000221703
    see all
  • 功能Acts as a molecular chaperone for mitochondrial complex I assembly.
  • 组织特异性Highly expressed in ESCC cells. Also expressed in heart, skeletal muscle, liver, and in fibroblasts.
  • 疾病相关Defects in NDUFAF2 are a cause of mitochondrial complex I deficiency (MT-C1D) [MIM:252010]. A disorder of the mitochondrial respiratory chain that causes a wide range of clinical disorders, from lethal neonatal disease to adult-onset neurodegenerative disorders. Phenotypes include macrocephaly with progressive leukodystrophy, non-specific encephalopathy, cardiomyopathy, myopathy, liver disease, Leigh syndrome, Leber hereditary optic neuropathy, and some forms of Parkinson disease.
  • 序列相似性Belongs to the complex I NDUFA12 subunit family.
  • 细胞定位Mitochondrion.
  • Information by UniProt

Recombinant Human Mimitin protein 图像

  • 15% SDS-PAGE analysis of 3 µg ab109967.

Recombinant Human Mimitin protein (ab109967)参考文献

ab109967 has not yet been referenced specifically in any publications.

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