Cy2DIGE NHS ester

英文名称：Cy2DIGE NHS ester

说明书安全数据表产品详情

价格 7092
产品规格

100 nmoles

产品货号

荧光标记探针经典荧光标记染料花菁合成试剂肽合成肽链标记试剂寡核苷酸合成试剂染料标记试剂

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产品参数

Ex (nm)	492	Em (nm)	508
分子量	677.50	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：Cy2DIGE 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：677.50

Ex:492nm

Em:508nm

溶剂：DMSO

产品介绍

Cy2DIGE NHS酯等同于Cy2®NHS酯基本染料，是用于标记DIGE蛋白分析的主要染料之一。Cy2DIGE通常与Cy3DIGE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Cy2DIGE 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
Authors: Wu, Y., Lam, C. S., Tse, D. Y., To, C. H., Liu, Q., McFadden, S. A., Chun, R. K., Li, K. K., Bian, J., Lam, C.
Journal: Mol Med Rep (2018): 5571-5580

Proteomic Analysis of Bovine Pregnancy-specific Serum Proteins by 2D Fluorescence Difference Gel Electrophoresis
Authors: Lee, J. E., Lee, J. Y., Kim, H. R., Shin, H. Y., Lin, T., Jin, D. I.
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
Authors: Hern, undefined and ez, C., Garcia-Ramirez, M., Colome, N., Corraliza, L., Garcia-Pascual, L., Casado, J., Canals, F., Simo, R.
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
Authors: Park, J., Oh, S., Park, S. B.
Journal: Angew Chem Int Ed Engl (2012): 5447-51