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
    • Accession
    • 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

图片

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

文献

ab109967 has not yet been referenced specifically in any publications.

客户评价及客户问答

There are currently no Customer reviews or Questions for ab109967.
Please use the links above to contact us or submit feedback about this product.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"

注册