Recombinant Human Ndufs4 protein (ab116433)

Overview

Description

  • NatureRecombinant
  • SourceEscherichia coli
  • Amino Acid Sequence
    • AccessionO43181
    • SpeciesHuman
    • SequenceMAQDQTQDTQ LITVDEKLDI TTLTGVPEEH IKTRKVRIFV PARNNMQSGV NNTKKWKMEF DTRERWENPL MGWASTADPL SNMVLTFSTK EDAVSFAEKN GWSYDIEERK VPKPKSKSYG ANFSWNKRTR VSTK
    • Molecular weight16 kDa
    • Amino acids43 to 175

Associated products

Specifications

Our Abpromise guarantee covers the use of ab116433 in the following tested applications.

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

  • Applications

    SDS-PAGE

  • Purity> 90 % SDS-PAGE.
    ab116433 was purified by proprietary chromatographic techniques and filter sterilized.
  • FormLiquid
  • Additional notesab116433 although stable 4°C for 4 weeks, should be stored desiccated below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please prevent freeze-thaw cycles.
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped at 4°C. Please see notes section.

    pH: 8.00
    Constituents: 0.32% Tris HCl, 30% Glycerol

General Info

  • Alternative names
    • AQDQ
    • CI 18
    • CI 18 kDa
    • CI AQDQ
    • CI-18 kDa
    • CI-AQDQ
    • Complex I 18 kDa
    • Complex I AQDQ
    • Complex I-18 kDa
    • Complex I-AQDQ
    • mitochondrial
    • mitochondrial respiratory chain complex I (18 KD subunit)
    • NADH coenzyme Q reductase
    • NADH dehydrogenase
    • NADH dehydrogenase (ubiquinone) Fe S protein 4 18kDa
    • NADH dehydrogenase [ubiquinone] iron-sulfur protein 4
    • NADH ubiquinone oxidoreductase 18 kDa subunit
    • NADH-ubiquinone oxidoreductase 18 kDa subunit
    • NDUFS4
    • NDUS4_HUMAN
    see all
  • FunctionAccessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in 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.
  • Involvement in diseaseDefects in NDUFS4 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.
  • Sequence similaritiesBelongs to the complex I NDUFS4 subunit family.
  • Cellular localizationMitochondrion inner membrane.
  • Information by UniProt

References for Recombinant Human Ndufs4 protein (ab116433)

ab116433 has not yet been referenced specifically in any publications.

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