Recombinant Human NDUFS7 Protein


SDS-Page: Recombinant Human NDUFS7 Protein [H00374291-P01] - 12.5% SDS-PAGE Stained with Coomassie Blue.

Product Details

Reactivity HuSpecies Glossary
Applications WB, ELISA, PA

Order Details

Recombinant Human NDUFS7 Protein Summary

A recombinant protein with GST-tag at N-terminal corresponding to the amino acids 1 - 213 of Human NDUFS7 full-length ORF

Source: Wheat Germ (in vitro)


Details of Functionality
This protein is not active and should not be used for experiments requiring activity.
Protein/Peptide Type
Recombinant Protein
>80% by SDS-PAGE and Coomassie blue staining


Application Notes
This protein has not been tested for any functionality. Product may contain endotoxins and is not suitable for use with live cells.

Packaging, Storage & Formulations

Store at -80C. Avoid freeze-thaw cycles.
50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
>80% by SDS-PAGE and Coomassie blue staining


This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for Recombinant Human NDUFS7 Protein

  • CI-20
  • CI-20kD
  • complex I, mitochondrial respiratory chain, 20-KD subunit
  • Complex I-20kD
  • EC
  • EC
  • EC
  • FLJ45860
  • FLJ46880
  • MGC120002
  • MY017
  • NADH dehydrogenase (ubiquinone) Fe-S protein 7 (20kD) (NADH-coenzyme Qreductase)
  • NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Qreductase)
  • NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial
  • NADH:ubiquinone oxidoreductase PSST subunit
  • NADH-coenzyme Q reductase
  • NADH-ubiquinone oxidoreductase 20 kDa subunit
  • PSST subunit
  • PSSTcomplex I 20kDa subunit


This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq]


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Peptides and proteins are guaranteed for 3 months from date of receipt.

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Gene Symbol NDUFS7