Glycogen Synthase 抗体
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- 抗原 See all Glycogen Synthase (GYS) 抗体
- Glycogen Synthase (GYS)
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Glycogen Synthase antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- This antibody detects endogenous levels of Glycogen Synthase protein. (region surrounding Pro539)
- 交叉反应 （详细）
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Species reactivity (expected):Mouse and Rat.
Species reactivity (tested):Human. - 纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
- 纯度
- > 95 % pure by SDS-PAGE
- Top Product
- Discover our top product GYS Primary Antibody
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anti-Glycogen Synthase (GYS) (AA 611-660), (pSer645) antibody
GYS 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Glycogen Synthase (GYS) (AA 621-670) antibodyGYS 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glycogen Synthase (GYS) (pSer641) antibodyGYS 适用: 人, 小鼠 WB, EIA, IP, IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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ELISA: 1: 5000approx. 1: 20000. WB: 1: 500approx. 1: 1000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - 限制
- 仅限研究用
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- 浓度
- 1.0 mg/mL
- 缓冲液
- Phosphate buffered saline (PBS), pH 7.2., 15 mM sodium azide
- 储存液
- Sodium azide
- 注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 注意事项
- DO NOT FREEZE!
- 储存条件
- 4 °C
- 储存方法
- Store the antibody undiluted at 2-8 °C.
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- 抗原
- Glycogen Synthase (GYS)
- 别名
- Glycogen Synthase (GYS 产品)
- 别名
- CG6940 antibody, Dmel\\CG6904 antibody, anon-WO0118547.108 antibody, glycogen synthase antibody, Glycogen synthase antibody, starch synthase antibody, glgA antibody, GlyS antibody, glgA-2 antibody, glgA-1 antibody, EAMY_RS33325 antibody, Hipma_0956 antibody, Tresu_1353 antibody, Spico_0935 antibody, Trebr_1511 antibody, Mahau_1987 antibody
- 背景
- Glycogen (starch) synthase belongs to the mammalian/fungal glycogen synthase family of proteins. Two forms of this protein exist, a liver form and a muscle form, both of which have the same function in the glycogen biosynthesis pathway. Glycogen synthase transfers the glycosyl residue from UDP-glucose to the nonreducing end of α-1,4-glucan. The 81 kDa liver glycogen synthase protein is truncated by 34 amino acids compared to the muscle form. However, these enzymes differ significantly in their amino- and carboxyl-terminal regions. Muscle glycogen synthase serves to fuel muscular activity only and is regulated by muscle contraction and by catecholamines. Liver glycogen synthase mediates blood glucose homeostasis in response to nutritional cues. Defects in the gene encoding liver glycogen synthase results in glycogen storage disease type 0 (GSD0), a rare form of fasting ketotic hypoglycemia.Synonyms: GYS, GYS1, muscle Glycogen Synthase
- 分子量
- approx. 84 kDa
- 基因ID
- 2997
- NCBI登录号
- NP_001155059
- UniProt
- P13807
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