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Probable peptide chain release factor

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Mitochondrial peptide chain release factor that directs the termination of translation in response to the peptide chain termination codons UAA and UAG.

Below are the list of possible Probable peptide chain release factor products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Probable peptide chain release factor 1

 Probable peptide chain release factor 1 ELISA Kit
 Probable peptide chain release factor 1 Recombinant
 Probable peptide chain release factor 1 Antibody
Also known as Probable peptide chain release factor 1, mitochondrial (MRF-1) (MtRF-1).
Mitochondrial peptide chain release factor that directs the termination of translation in response to the peptide chain termination codons UAA and UAG.
 W03F8.3 ELISA Kit
 W03F8.3 Recombinant
 W03F8.3 Antibody
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Probable peptide chain release factor C12orf65 homolog

 Probable peptide chain release factor C12orf65 homolog ELISA Kit
 Probable peptide chain release factor C12orf65 homolog Recombinant
 Probable peptide chain release factor C12orf65 homolog Antibody
Also known as Probable peptide chain release factor C12orf65 homolog, mitochondrial.
May act as a codon-independent translation release factor that has lost all stop codon specificity and directs the termination of translation in mitochondrion. May help rescuing stalled mitoribosomes during translation ().
 si:ch211-275j6.5 ELISA Kit
 si:ch211-275j6.5 Recombinant
 si:ch211-275j6.5 Antibody
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Probable peptide chain release factor C12orf65

 Probable peptide chain release factor C12orf65 ELISA Kit
 Probable peptide chain release factor C12orf65 Recombinant
 Probable peptide chain release factor C12orf65 Antibody
Also known as Probable peptide chain release factor C12orf65, mitochondrial.
C12orf65: May act as a codon-independent translation release factor that has lost all stop codon specificity and directs the termination of translation in mitochondrion. Defects in C12orf65 are the cause of combined oxidative phosphorylation deficiency type 7 (COXPD7). A mitochondrial disease resulting in encephalomyop
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athy. Clinical manifestations include psychomotor delay and regression, ataxia, optic atrophy, nystagmus and muscle atrophy and weakness. Belongs to the prokaryotic/mitochondrial release factor family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: RNA-binding; Translation

Chromosomal Location of Human Ortholog: 12q24.31

Cellular Component: mitochondrial large ribosomal subunit

Molecular Function: aminoacyl-tRNA hydrolase activity; ribosome binding; translation release factor activity, codon nonspecific; translation release factor activity, codon specific

Disease: Combined Oxidative Phosphorylation Deficiency 7
 C12orf65 ELISA Kit
 C12orf65 Recombinant
 C12orf65 Antibody
 My030 ELISA Kit
 My030 Recombinant
 My030 Antibody
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