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Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Additionally we are shipping GFM1 Kits (7) and GFM1 Proteins (5) and many more products for this protein.
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Sequencing of EFG1 revealed a mutation affecting a conserved residue of the guanosine triphosphate (GTP)-binding (show RND2 Antibodies) domain. These results define a new class of gene defects underlying disorders of oxidative phosphorylation.
mutations in the mitochondrial translation factor EFG1 may have a role in oxidative phosphorylation deficiencies [case report]
Genetic investigation of patients with defective mitochondrial translation led to the discovery of novel mutations in the mitochondrial elongation factor G1 (EFG1) in one affected baby and in the mitochondrial elongation factor Tu (show EEF1A1 Antibodies) (EFTu (show Tufm Antibodies)) in another one
Eukaryotes contain two protein translational systems, one in the cytoplasm and one in the mitochondria. Mitochondrial translation is crucial for maintaining mitochondrial function and mutations in this system lead to a breakdown in the respiratory chain-oxidative phosphorylation system and to impaired maintenance of mitochondrial DNA. This gene encodes one of the mitochondrial translation elongation factors. Its role in the regulation of normal mitochondrial function and in different disease states attributed to mitochondrial dysfunction is not known.
, G translation elongation factor, mitochondrial
, elongation factor G 1, mitochondrial
, elongation factor G, mitochondrial
, elongation factor G1
, mEF-G 1
, mitochondrial elongation factor G
, mitochondrial elongation factor G1
, G elongation factor 1