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GFM1 Antibody (C-term) Blocking peptide

Synthetic peptide

Product Information
Primary Accession Q96RP9
Clone Names 91102306
Peptide ID 91102306
Additional Information
Gene ID 85476
Other Names Elongation factor G, mitochondrial {ECO:0000255|HAMAP-Rule:MF_03061}, EF-Gmt {ECO:0000255|HAMAP-Rule:MF_03061}, Elongation factor G 1, mitochondrial {ECO:0000255|HAMAP-Rule:MF_03061}, mEF-G 1 {ECO:0000255|HAMAP-Rule:MF_03061}, Elongation factor G1 {ECO:0000255|HAMAP-Rule:MF_03061}, hEFG1, GFM1 {ECO:0000255|HAMAP-Rule:MF_03061}
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name GFM1 {ECO:0000255|HAMAP-Rule:MF_03061}
Function Mitochondrial GTPase that catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A- site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome. Does not mediate the disassembly of ribosomes from messenger RNA at the termination of mitochondrial protein biosynthesis.
Cellular Location Mitochondrion {ECO:0000255|HAMAP- Rule:MF_03061}
Research Areas
Citations (0)

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Eukaryotes contain two protein translational systems, onein the cytoplasm and one in the mitochondria. Mitochondrialtranslation is crucial for maintaining mitochondrial function andmutations in this system lead to a breakdown in the respiratorychain-oxidative phosphorylation system and to impaired maintenanceof mitochondrial DNA. This gene encodes one of the mitochondrialtranslation elongation factors. Its role in the regulation ofnormal mitochondrial function and in different disease statesattributed to mitochondrial dysfunction is not known. [provided byRefSeq].


Shuen, A.Y., et al. Clin. Chim. Acta 409 (1-2), 28-32 (2009) :Tsuboi, M., et al. Mol. Cell 35(4):502-510(2009)Valente, L., et al. Am. J. Hum. Genet. 80(1):44-58(2007)Antonicka, H., et al. Hum. Mol. Genet. 15(11):1835-1846(2006)Coenen, M.J., et al. N. Engl. J. Med. 351(20):2080-2086(2004)

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$ 80.00
Cat# BP10753b
Availability: In Stock
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