Glycogen synthase 1/GYS1多肽(ab204860)
Key features and details
- Purity: > 95% HPLC
- Suitable for: Functional Studies, HPLC
描述
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产品名称
Glycogen synthase 1/GYS1多肽
参阅全部 Glycogen synthase 1/GYS1 蛋白酶 -
纯度
> 95 % HPLC. -
无动物成分
No -
性质
Synthetic -
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序列
YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE -
氨基酸
636 to 661
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技术指标
Our Abpromise guarantee covers the use of ab204860 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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应用
Functional Studies
HPLC
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形式
Lyophilized -
补充说明
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Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Store at -20°C. Avoid freeze / thaw cycle.
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复溶Dilute peptide in 25mM Tris-HCl, pH 7.5 solution to a final concentration of 1 mg/ml. For optimal storage, aliquot diluted product into smaller quantities and store at recommended temperature.
常规信息
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别名
- Glycogen [starch] synthase
- Glycogen synthase 1
- Glycogen synthase 1 (muscle)
see all -
功能
Transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan. -
通路
Glycan biosynthesis; glycogen biosynthesis. -
疾病相关
Defects in GYS1 are the cause of muscle glycogen storage disease type 0 (GSD0b) [MIM:611556]; also known as muscle glycogen synthase deficiency. GSD0b is a metabolic disorder characterized by fasting hypoglycemia presenting in infancy or early childhood. The role of muscle glycogen is to provide critical energy during bursts of activity and sustained muscle work. -
序列相似性
Belongs to the glycosyltransferase 3 family. - Information by UniProt
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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Datasheet download
文献 (0)
ab204860 尚未被引用在任何文献中。