Recombinant Human COQ7 (C-6His)
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| Amount : | 50 µg |
| Content : | Supplied as a 0.2 um filtered solution of 20mM PB, 150mM NaCl, pH 7.4 |
| AA sequence : | Recombinant Human 5-demethoxyubiquinone hydroxylase, mitochondrial is produced by our Mammalian expression system and the target gene encoding Ser37-Leu217 is expressed with a 6His tag at the C-terminus. |
| Alternative Name : | Ubiquinone Biosynthesis Protein COQ7 Homolog; Coenzyme Q Biosynthesis Protein 7 Homolog; Timing Protein Clk-1 Homolog; 5-demethoxyubiquinone hydroxylase; COQ7 |
Source : Human Cells;
Ubiquinone Biosynthesis Protein COQ7 Homolog is a mitochondrion inner membrane and peripheral membrane protein that belongs to the COQ7 family. It is expressed primarily in heart and skeletal muscle. COQ7 is synthesized as a preprotein that is transmitted into the mitochondrial matrix, where the sequence is cleaved off and the mature protein becomes loosely associated with the inner membrane. COQ7 plays a role in lifespan determination in ubiquinone-independent manner, as well as ubiquinone biosynthesis. COQ7 also acts as a potential central metabolic regulator. It has been shown that mutations in the gene are associated with increased life span. Defects of the gene slow down a variety of developmental and physiological processes, including the cell cycle, embryogenesis, post-embryonic growth, rhythmic behaviors and aging.
Ubiquinone Biosynthesis Protein COQ7 Homolog is a mitochondrion inner membrane and peripheral membrane protein that belongs to the COQ7 family. It is expressed primarily in heart and skeletal muscle. COQ7 is synthesized as a preprotein that is transmitted into the mitochondrial matrix, where the sequence is cleaved off and the mature protein becomes loosely associated with the inner membrane. COQ7 plays a role in lifespan determination in ubiquinone-independent manner, as well as ubiquinone biosynthesis. COQ7 also acts as a potential central metabolic regulator. It has been shown that mutations in the gene are associated with increased life span. Defects of the gene slow down a variety of developmental and physiological processes, including the cell cycle, embryogenesis, post-embryonic growth, rhythmic behaviors and aging.
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