Background：This gene encodes an nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase （complex I, or NADH：ubiquinone oxidoreductase）. Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants.
仕様
Synonyms：AQDQ,CI 18,CI 18 kDa,CI AQDQ,CI-18 kDa,CI-AQDQ,Complex I 18 kDa,Complex I AQDQ,Complex I-18 kDa,Complex I-AQDQ,mitochondrial,mitochondrial respiratory chain complex I （18 KD subunit）,NADH coenzyme Q reductase,NADH dehydrogenase （ubiquinone） Fe S protein 4 18kDa,NADH dehydrogenase [ubiquinone] iron-sulfur protein 4,NADH dehydrogenase,NADH ubiquinone oxidoreductase 18 kDa subunit,NADH-ubiquinone oxidoreductase 18 kDa subunit,NDUFS4,NDUS4
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human NDUFS4
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
Dilution：WB1：500 - 1：2000
Gene_ID（human）：4724
Swissprot：O43181
Isotype：IgG
Research Areas：Cancer, Metabolism, Neuroscience, Signal transduction
