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Cy3DIGE NHS ester

英文名称:Cy3DIGE NHS ester
产品参数
Ex (nm)555Em (nm)569
分子量709.67溶剂DMSO
存储条件在零下15度以下保存, 避免光照
产品概述

产品基本信息

产品名称:Cy3DIGE NHS ester

储存条件:-15℃避光防潮

保质期:24个月

 

产品物理化学光谱特性

分子量:709.67

Ex:555nm

Em:569nm

溶剂:DMSO

 

产品介绍

Cy3DIGE NHS酯等同于Cy3®NHS酯基本染料,是用于标记DIGE蛋白分析的主要染料之一。Cy3DIGE通常与Cy2DIGE和Cy5DIGE一起使用。Cy2DIGE,C3DIGE和Cy5DIGE是专为比较两个或三个裂解液样品中蛋白质表达而设计的。匹配迁移率和明亮的染料荧光使2D凝胶电泳能够有效检测和微量蛋白质的高分辨率分离。Cy2DIGE,C3DIGE和Cy5DIGE与所有能够检测Cy2,Cy3和Cy5的染料成像仪兼容。Cy2DIGE,C3DIGE和Cy5DIGE标记的凝胶是规格匹配、电荷匹配的荧光染料,用于检测二维荧光差异凝胶电泳(DIGE)中的蛋白质丰度差异。Cy2DIGE C3DIGE和Cy5DIGE在同一2-D电泳凝胶上多可检测三个预先标记的蛋白质样品和标准品。规格和电荷匹配的染料可以使标记的样品在凝胶内共迁移。它们在标记的蛋白质上很亮,可以在标记、分离和扫描过程中将信号损失降至低。这些染料的光谱重叠很少,可将通常导致高背景的串扰降至低。它们对pH值不敏感的荧光使DIGE可以在较宽的pH范围内运行。百萤生物是AAT Bioquest的中国代理商,为您提供优质的Cy3DIGE NHS ester。 

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参考文献

LncRNA AL592284. 1 facilitates proliferation and metastasis of cervical cancer cells via miR-30a-5p/Vimentin/EMT axis
Authors: Zhang, Jing and Liu, Hong-li and Liu, Jing-bo and Zhang, Yuan and Liu, Jing and Li, Yan-hua
Journal: Biochemical and Biophysical Research Communications (2021): 95--102
 
Early quantitative profiling of differential retinal protein expression in lens-induced myopia in guinea pig using fluorescence difference two-dimensional gel electrophoresis
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Proteomic Analysis of Bovine Pregnancy-specific Serum Proteins by 2D Fluorescence Difference Gel Electrophoresis
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Journal: Asian-Australas J Anim Sci (2015): 788-95
 
Comparative proteomic analysis of different Toxoplasma gondii genotypes by two-dimensional fluorescence difference gel electrophoresis combined with mass spectrometry
Authors: Zhou, D. H., Zhao, F. R., Nisbet, A. J., Xu, M. J., Song, H. Q., Lin, R. Q., Huang, S. Y., Zhu, X. Q.
Journal: Electrophoresis (2014): 533-45
 
Comparative proteomic analysis of Dan'er malts produced from distinct malting processes by two-dimensional fluorescence difference in gel electrophoresis (2D-DIGE)
Authors: Li, X., Jin, Z., Gao, F., Lu, J., Cai, G., Dong, J., Yu, J., Yang, M.
Journal: J Agric Food Chem (2014): 9310-6
 
Proteomic analysis of the hippocampus in Alzheimer's disease model mice by using two-dimensional fluorescence difference in gel electrophoresis
Authors: Takano, M., Yamashita, T., Nagano, K., Otani, M., Maekura, K., Kamada, H., Tsunoda, S., Tsutsumi, Y., Tomiyama, T., Mori, H., Matsuura, K., Matsuyama, S.
Journal: Neurosci Lett (2013): 85-9
 
Application of fluorescence two-dimensional difference in-gel electrophoresis as a proteomic biomarker discovery tool in muscular dystrophy research
Authors: Carberry, S., Zweyer, M., Sw and ulla, D., Ohlendieck, K.
Journal: Biology (Basel) (2013): 1438-64
 
Two-dimensional fluorescence difference gel electrophoresis analysis of Listeria monocytogenes submitted to a redox shock
Authors: Ignatova, M., Guevel, B., Com, E., Haddad, N., Rossero, A., Bogard, P., Prevost, H., Guillou, S.
Journal: J Proteomics (2013): 13-27
 
Identification of new pathogenic candidates for diabetic macular edema using fluorescence-based difference gel electrophoresis analysis
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Journal: Diabetes Metab Res Rev (2013): 499-506
 
Discovery and target identification of an antiproliferative agent in live cells using fluorescence difference in two-dimensional gel electrophoresis
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Journal: Angew Chem Int Ed Engl (2012): 5447-51