Human NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial) ELISA Kit
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name
Human NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial) ELISA Kit
category
ELISA Kits
provider
FineTest
reference
EH1842
tested applications
ELISA
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | ELISA Kits |
| Reactivity | Human |
| Detection Method | Colorimetric |
| Assay Data | 4 hours |
| Assay Type | Sandwich ELISA, Double Antibody |
| Test Range | 0.313-20ng/ml |
| Sensitivity | 0.188ng/ml |
| Size 1 | 96T |
| Tested Applications | ELISA |
| Sample Type | Serum, Plasma, Cell Culture Supernatant, cell or tissue lysate, Other liquid samples |
| Availability | Shipped within 10-14 working days. |
| Storage | 2-8 °C for 12 months |
| UniProt ID | O75251 |
| Alias | NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial, Complex I-20kD, CI-20kD, NADH-ubiquinone oxidoreductase 20 kDa subunit, PSST subunit, NDUFS7 |
| Background | Elisa kits for NDUFS7 |
| Status | RUO |
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Human NDUFS7 (NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial) ELISA Kit
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NDUFS7 antibody
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.
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