NDUFS7 polyclonal, anti-human, mouse

Background:
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.

Synonyms: PSST, CI-20, MY017, CI-20KD

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human NDUFS7

Gene Symbol: NDUFS7

Gene ID: 374291

Swiss prot: O75251

Calculated MW: 24kDa

Recommended dilution:
IHC 1:10-100

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.