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  2. Polyclonal

GTX88036

NDUFS7 antibody, Internal

Cannot supply to this region.

SKU:
GTX88036
Additional Names:
NADH:ubiquinone oxidoreductase core subunit S7 , CI-20 , CI-20KD , MC1DN3 , MY017 , PSST
Application:
WB
Concentration:
0.50 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Ammonium Sulfate Precipitated; Affinity Purified
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
Host:
Goat
Reactivities:
Human
Buffer:
TBS, 0.5% BSA, 0.02% Sodium azide.
Immunogen:
Peptide with sequence C-SRGEYVVAKLD, from the internal region of the protein sequence according to NP_077718.3.
Uniprot:
O75251
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