NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5)

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C20orf7; Probable methyltransferase C20orf7, mitochondrial

NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5)
The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. This gene encodes a mitochondrial protein that is associated with the matrix face of the mitochondrial inner membrane and is required for complex I assembly. A mutation in this gene results in mitochondrial complex I deficiency. Multiple transcript variants encoding different isoforms have been found for this gene. Knockdown of C20ORF7 decreased complex I activity and that C20ORF7 is involved in the assembly or stability of an early complex I assembly intermediate that contains the ND1 subunit. In vitro transcription and translation studies showed that the full-length 39-kD protein associated with mitochondria.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) CLIA Kit Customized Service Offer
n/a ELISA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) CLIA Kit Customized Service Offer
n/a ELISA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) CLIA Kit Customized Service Offer
n/a ELISA Kit for NADH Dehydrogenase Ubiquinone 1 Alpha Subcomplex Assembly Factor 5 (NDUFaF5) ELISA Kit Customized Service Offer
  1. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  2. "The DNA sequence and comparative analysis of human chromosome 20." Nature 414:865-871(2001) [PubMed] [Europe PMC] [Abstract]
  3. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  4. "Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease."Am. J. Hum. Genet. 83:468-478(2008) [PubMed] [Europe PMC] [Abstract]
  5. "Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome."J. Med. Genet. 47:507-512(2010) [PubMed] [Europe PMC] [Abstract]