GTX88036-PEP
NDUFS7 blocking peptide
Cannot supply to this region.
- SKU:
- GTX88036-PEP
- Additional Names:
- Nadh:Ubiquinone Oxidoreductase Core Subunit S7 , Ci-20 , Ci-20Kd , My017 , Psst , Ndufs7
- Physical State:
- Lyophilized
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Buffer:
- Reconstitute with 200ul distilled water to obtain a 0.5mg/ml peptide solution. Lyophilized from 5% (v/v) acetonitrile/H₂O, no preservatives.
- Immunogen:
- NADH:ubiquinone oxidoreductase core subunit S7
- Species:
- Human
- Synonyms:
- CI-20;CI-20KD;complex I 20kDa subunit;complex I-20kD;complex I, mitochondrial respiratory chain, 20-KD subunit;MC1DN3;MY017;NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase);NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial;NADH-coenzyme Q reductase;NADH-ubiquinone oxidoreductase 20 kDa subunit;NADH:ubiquinone oxidoreductase PSST subunit;PSST;PSST subunit
- Extra Details:
- 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, Jul 2008]
- Shipping Conditions:
- Blue Ice