Recombinant Human Mimitin protein (ab109967)

製品の概要

  • 製品名Recombinant Human Mimitin protein
  • タンパク質長Full length protein

製品の詳細

  • 由来Recombinant
  • 由来Escherichia coli
  • アミノ酸配列
    • アクセッション番号Q8N183
    • 生物種Human
    • 配列MGSSHHHHHHSSGLVPRGSHMGWSQDLFRALWRSLSREVKEHVGTDQFGN KYYYIPQYKNWRGQTIREKRIVEAANKKEVDYEAGDIPTEWEAWIRRTRK TPPTMEEILKNEKHREEIKIKSQDFYEKEKLLSKETSEELLPPPVQTQIK GHASAPYFGKEEPSVAPSSTGKTFQPGSWMPRDGKSHNQ
    • 分子量22 kDa including tags
    • 領域1 to 169
    • タグHis tag N-Terminus

特性

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.

  • アプリケーション

    SDS-PAGE

    Mass Spectrometry

  • 質量分析
    MALDI-TOF
  • 精製度> 85 % SDS-PAGE.
    ab109967 was purified using conventional chromatography techniques.
  • 製品の状態Liquid
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    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

関連情報

  • 別名
    • 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
  • 機能Acts as a molecular chaperone for mitochondrial complex I assembly.
  • 組織特異性Highly expressed in ESCC cells. Also expressed in heart, skeletal muscle, liver, and in fibroblasts.
  • 関連疾患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.
  • 配列類似性Belongs to the complex I NDUFA12 subunit family.
  • 細胞内局在Mitochondrion.
  • Information by UniProt

Recombinant Human Mimitin protein 画像

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

Recombinant Human Mimitin protein (ab109967) 使用論文

ab109967 has not yet been referenced specifically in any publications.

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