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.

Classification:

Primary antibody

Alternative names:

NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial ;Complex I-18 kDa;CI-18 kDa;Complex I-AQDQ;CI-AQDQ;NADH-ubiquinone oxidoreductase 18 kDa subunit

Species reactivity:

Human, Rat, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human protein . at AA range: 20-100

Concentration:

1 mg/ml

Molecular weight:

Applications:

WB, ELISA

Storage:

-20°C for 1 year

More info:

Email: info@sobekbio.com

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