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NDUFS3 Polyclonal Antibody, 100ul Immunoassays This complex functions through chromatin

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NDUFS3 Polyclonal Antibody, 100ul Immunoassays This complex functions through chromatinNDUFS3 encodes one of the iron sulfur protein (IP) components of mitochondrial NADH: ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.

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Description

This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells

The protein encoded by this gene is an RNA lariat debranching enzyme that hydrolyzes 2'-5' prime branched phosphodiester bonds

Mutations in paired box gene 3 are associated with Waardenburg syndrome

CYP17A1 encodes a member of the cytochrome P450 superfamily of enzymes

including heart rate in cardiac cells and circuit activity in neuronal cells

NDUFS3 Polyclonal Antibody, 100ul Immunoassays This complex functions through chromatinNDUFS3 encodes one of the iron sulfur protein (IP) components of mitochondrial NADH: ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.

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