
WB analysis of human heart lysate using GTX88036 NDUFS7 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
NDUFS7 antibody, Internal
GTX88036
Overview
- SupplierGeneTex
- Product NameNDUFS7 antibody, Internal
- Delivery Days Customer9
- Application Supplier NoteWB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsWestern Blot
- CertificationResearch Use Only
- ClonalityPolyclonal
- Concentration0.50 mg/ml
- ConjugateUnconjugated
- Gene ID374291
- Target nameNDUFS7
- Target descriptionNADH:ubiquinone oxidoreductase core subunit S7
- Target synonymsCI-20; CI-20KD; complex I 20kDa subunit; complex I, mitochondrial respiratory chain, 20-KD subunit; complex I-20kD; MC1DN3; MY017; NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial; NADH:ubiquinone oxidoreductase PSST subunit; NADH-coenzyme Q reductase; NADH-ubiquinone oxidoreductase 20 kDa subunit; PSST; PSST subunit
- HostGoat
- IsotypeIgG
- Protein IDO75251
- Protein NameNADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial
- Scientific DescriptionThis 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, Jul 2008]
- ReactivityHuman
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203