NDUFS2 blocking peptide

NDUFS2 Antibody (Center) Blocking Peptide

• Gene Names: NDUFS2; CI-49
• Synonyms: NDUFS2; NDUFS2 Antibody (Center) Blocking Peptide; NADH dehydrogenase [ubiquinone] iron-sulfur protein 2; mitochondrial; Complex I-49kD; CI-49kD; NADH-ubiquinone oxidoreductase 49 kDa subunit; NDUFS2 blocking peptide

• Form/Format: Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
• Sequence Length: 463

• Cellular Location: Mitochondrion inner membrane; Peripheral membrane protein; Matrix side
• Preparation and Storage: Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C.

Related Product Information for NDUFS2 blocking peptide

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 (By similarity).

NCBI and Uniprot Product Information

• NCBI GI #: 20178314
• NCBI GeneID: 4720
• UniProt Accession #: O75306; Q5VTW0; Q969P3; Q9UEV3; D3DVG7; J3KPM7
• Molecular Weight: 51,852 Da
• NCBI Official Full Name: NADH dehydrogenase
• NCBI Official Synonym Full Names: NADH:ubiquinone oxidoreductase core subunit S2
• NCBI Official Symbol: NDUFS2
• NCBI Official Synonym Symbols: CI-49
• NCBI Protein Information: NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial
• UniProt Protein Name: NADH dehydrogenase [ubiquinone] iron-sulfur protein 2, mitochondrial
• UniProt Gene Name: NDUFS2
• UniProt Synonym Gene Names: CI-49kD
• UniProt Entry Name: NDUS2_HUMAN

NCBI Description

The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]

Uniprot Description

NDUFS2: 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. Defects in NDUFS2 are a cause of mitochondrial complex I deficiency (MT-C1D). 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. Belongs to the complex I 49 kDa subunit family.

Protein type: Oxidoreductase; Mitochondrial; EC 1.6.5.3; EC 1.6.99.3; Energy Metabolism - oxidative phosphorylation

Chromosomal Location of Human Ortholog: 1q23

Cellular Component: mitochondrial matrix; mitochondrial respiratory chain complex I; mitochondrion; nucleoplasm

Molecular Function: NADH dehydrogenase activity; protein binding; ubiquitin protein ligase binding

Biological Process: mitochondrial electron transport, NADH to ubiquinone; mitochondrial respiratory chain complex I assembly; response to oxidative stress

Disease: Mitochondrial Complex I Deficiency