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・ Glycogen storage disease type I
・ Glycogen storage disease type II
・ Glycogen storage disease type III
・ Glycogen storage disease type IV
・ Glycogen storage disease type IX
・ Glycogen storage disease type V
・ Glycogen storage disease type VI
・ Glycogen storage disease type XI
・ Glycogen synthase
・ Glycogen synthase kinase
・ Glycogen-branching enzyme deficiency
・ Glycogenase
・ Glycogenesis
・ Glycogenic acanthosis
・ Glycogenin
Glycogenin-1
・ Glycogenolysis
・ Glycoinformatics
・ Glycol cleavage
・ Glycol dehydration
・ Glycol distearate
・ Glycol ethers
・ Glycol nucleic acid
・ Glycol stearate
・ Glycolaldehyde
・ Glycolaldehyde dehydrogenase
・ Glycolate dehydrogenase
・ Glycolic acid
・ Glycolipid
・ Glycolipid 2-alpha-mannosyltransferase


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Glycogenin-1 : ウィキペディア英語版
Glycogenin-1

Glycogenin-1 is an enzyme that is involved in the biosynthesis of glycogen. This enzyme is important for the function of self-glucosylated to form an oligosaccharide primer that serves as substrate for glycogen synthase. This is done through an inter-subunit mechanism. It also plays a role in glycogen metabolism regulation and in the maximal glycogen levels attaintment in skeletal muscle. Recombinant human glycogenin-1 was expressed in ''E. coli'' and purified by using conventional chromatography techniques.〔Details for Glycogenin-1, 1-333 aa, Recombinant Protein. ().〕
==Introduction: glycogen metabolism==

Glycogen is a multi branched polysaccharide. It is the way all the animal cells have to store glucose. In the human body, the two main tissues of glycogen accumulation are liver and skeletal muscle. The concentration of this polysaccharide is superior at the liver, but, due to the major mass of skeletal that muscle humans have, this tissue contains three quarters of the corporal glycogen.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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