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ACADL Rabbit Polyclonal Antibody, 20ul Low retention tips an inherited retinopathy

SKU: 70501308971

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ACADL Rabbit Polyclonal Antibody, 20ul Low retention tips an inherited retinopathyThe protein encoded by this gene belongs to the acyl CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta oxidation of straight chain fatty acid. Defects in this gene are the cause of long chain acyl CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

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Description

an inherited retinopathy

RPL10 encodes a ribosomal protein that is a component of the 60S ribosome subunit

Induces stromal cells to produce proinflammatory and hematopoietic cytokines

cullin (see CUL1

The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose| but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids

ACADL Rabbit Polyclonal Antibody, 20ul Low retention tips an inherited retinopathyThe protein encoded by this gene belongs to the acyl CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta oxidation of straight chain fatty acid. Defects in this gene are the cause of long chain acyl CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

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