Description
Product Characteristics: For quantitative detection of EEF1A1 in serum, plasma, tissue homogenates.
Target Information: This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. [provided by RefSeq, Jul 2008]