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Merck
CN

MAK016

糖原检测试剂盒

sufficient for 100 colorimetric or fluorometric tests

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关于此项目

NACRES:
NA.84
UNSPSC Code:
12161503
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usage

sufficient for 100 colorimetric or fluorometric tests

detection method

colorimetric, fluorometric

storage temp.

−20°C

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General description

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。

Application

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。

Biochem/physiol Actions

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。

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

存储类别

10 - Combustible liquids

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
Long-term obestatin treatment of mice type 2 diabetes increases insulin sensitivity and improves liver function.
Kolodziejski P A, et al.
Endocrine, 56(3), 538-550 (2017)
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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