Recombinant Human NDUFV1 protein (ab117059)

製品の概要

製品の詳細

  • 由来Recombinant
  • 由来Wheat germ
  • アミノ酸配列
    • アクセッション番号P49821
    • 生物種Human
    • 配列KAIARLIEFYKHESCGQCTPCREGVDWMNKVMARFVRGDARPAEIDSLWE ISKQIEGHTICALGDGAAWPVQGLIRHFRPELEERMQRFAQQHQARQAAS
    • 分子量37 kDa including tags
    • 領域365 to 464

関連製品

特性

Our Abpromise guarantee covers the use of ab117059 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

    Western blot

    SDS-PAGE

    ELISA

  • 製品の状態Liquid
  • 備考Protein concentration is above or equal to 0.05 mg/ml.
    Best used within three months from the date of receipt.
  • Concentration information loading...

前処理および保存

  • 保存方法および安定性

    Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.

    pH: 8.00
    Constituents: 0.3% Glutathione, 0.79% Tris HCl

関連情報

  • 別名
    • CI 51kD
    • CI-51kD
    • Complex I 51kD
    • Complex I-51kD
    • FLJ59059
    • mitochondrial
    • NADH dehydrogenase (ubiquinone) flavoprotein 1
    • NADH dehydrogenase [ubiquinone] flavoprotein 1
    • NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial
    • NADH dehydrogenase flavoprotein 1
    • NADH ubiquinone oxidoreductase
    • NADH ubiquinone oxidoreductase 51 kDa subunit
    • NADH-ubiquinone oxidoreductase 51 kDa subunit
    • NDUFV 1
    • ndufv1
    • NDUV1_HUMAN
    • UQOR1
    see all
  • 機能Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.
  • 関連疾患Defects in NDUFV1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.
    Defects in NDUFV1 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 51 kDa subunit family.
  • 細胞内局在Mitochondrion inner membrane.
  • Information by UniProt

Recombinant Human NDUFV1 protein 画像

  • 12.5% SDS-PAGE showing ab117059 at approximately 36.63 kDa.
    Stained with Coomassie Blue.

Recombinant Human NDUFV1 protein (ab117059) 使用論文

ab117059 has not yet been referenced specifically in any publications.

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