用途
sufficient for 100 colorimetric or fluorometric tests
检测方法
colorimetric
fluorometric
储存温度
−20°C
一般描述
糖原是一种葡萄糖支链聚合物，是动物体内主要短期能量储存分子。 糖原主要在肝脏和肌肉组织中合成，占肝脏重量的10%和肌肉重量的1-2%。 当肌肉糖原通常就被肌肉使用，而肝脏糖原是调节血液葡萄糖水平的重要缓冲液。 糖尿病和因为先天代谢缺陷导致的糖原储存疾病，会导致糖原代谢失调。
应用
糖原分析试剂盒可用于糖原定量分析。它用于确定肝脏，股外侧肌和肌肉匀浆中糖原含量。
适合于确定各种组织，比如肝脏等和细胞培养（粘附或悬浮细胞）中糖原浓度。
生化/生理作用
糖原代谢能够被偶联酶分析检测，生成的比色（570nm）/荧光 (λex = 535/λem = 587 nm)产物和葡萄含糖原量成正比。
警示用语：
Danger
危险声明
危险分类
Resp. Sens. 1 - Skin Sens. 1
储存分类代码
10 - Combustible liquids
闪点(°F)
188.6 °F - closed cup
闪点(°C)
87 °C - closed cup
法规信息
常规特殊物品
此项目有
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Insulin Signaling in Bupivacaine-induced Cardiac ToxicitySensitization during Recovery and Potentiation by Lipid Emulsion
Fettiplace M R, et al.
Anesthesiology, 124(2), 428-\442-428-\442 (2016)
Madhuri S Salker et al.
Scientific reports, 7(1), 12612-12612 (2017-10-05)
Embryo implantation requires a hospitable uterine environment. A key metabolic change that occurs during the peri-implantation period, and throughout early pregnancy, is the rise in endometrial glycogen content. Glycogen accumulation requires prior cellular uptake of glucose. Here we show that
Cassius E O Coombs et al.
Meat science, 134, 86-97 (2017-08-05)
This study evaluated the effect of chilled followed by frozen storage on lamb quality and safety parameters. Experimental (n=360) M. longissimus lumborum (LL) were randomly sampled from the boning room of a commercial Australian abattoir, at 24 h post-mortem, and
Nuwan A L De Silva et al.
Ecotoxicology and environmental safety, 158, 274-283 (2018-05-02)
Freshwater pulmonate snails are sensitive to trace metals, but to date, the sensitivity of estuarine pulmonate snails to these important environmental toxicants is undescribed. Using the estuarine mud snail Amphibola crenata, effects of a 48-h exposure to waterborne cadmium (Cd)
Nady Golestaneh et al.
Journal of translational medicine, 14(1), 344-344 (2016-12-22)
Study of age related macular degeneration (AMD) has been hampered by lack of human models that represent the complexity of the disease. Here we have developed a human in vitro disease model of AMD to investigate the underlying AMD disease
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