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Sulfo-Cyanine7 NHS ester

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  • 产品名称:Sulfo-Cyanine7 NHS ester
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  • 产品展商:Lumiprobe
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简单介绍

Sulfo-Cyanine7 NHS ester

产品描述

 

订购货号 产品名称及规格 价格(¥)
15320 Sulfo-Cyanine7 NHS ester, 1 mg 2080.00
25320 Sulfo-Cyanine7 NHS ester, 5 mg 5330.00
45320 Sulfo-Cyanine7 NHS ester, 25 mg 11050.00
55320 Sulfo-Cyanine7 NHS ester, 50 mg 19500.00
65320 Sulfo-Cyanine7 NHS ester, 100 mg 31850.00

 

 


水溶近红外染料sulfo-Cyanine7,是胺类活性琥珀酸亚胺酯。


Sulfo-Cyanine7是Cy7®荧光团的的改良衍生物,量子产率提高20%,并具有更好的耐光性。该染料尤其适用于NIR成像应用。


近红外荧光染料利用了生物组织在特定的波长范围里的透明度。这种方法是无损伤性的,并允许在活体内对多种已标记的生物分子的分布进行跟踪。


Sulfo-Cyanine7 NHS ester可以很轻松的标记生物分子,如:蛋白质。标记的分子可以用于后续多种研究及**开发相关的实验。


这种染料有很高的水溶解度,尤其适用于痕量蛋白质和易变性蛋白质的标记。需有机溶剂才能溶解的非磺化的Cyanine7 NHS ester。
 

 

 

 

Sulfo-Cyanine7 NHS ester

 

推荐手册:

氨基分子的NHS酯标记

 

Cy® is a trademark of GE Healthcare.


General properties

 

Appearance:

dark green powder

Molecular weight:

827.94

Molecular formula:

C41H46N3NaO10S2

Solubility:

good in water, DMF, DMSO

Quality control:

NMR 1H (95%) and 13C, TLC, functional testing

Storage conditions:

Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate.

MSDS:

Download

Spectral properties

 

Excitation maximum, nm:

740

Extinction coefficient at excitation maximum, Lmol-1cm-1:

240600

Emission maximum, nm:

773

CF260:

0.04

CF280:

0.04

 


Product citations

  • Ayala-Orozco, C.; Liu, J.G.; Knight, M.W.; Wang, Y.; Day, J.K.; Nordlander, P.; Halas, N.J. Fluorescence Enhancement of Molecules Inside a Gold Nanomatryoshka. Nano Letters, 2014, 14(5), 2926-2933. doi: 10.1021/nl501027j
  • Brand, C.; Abdel-Atti, D.; Zhang, Y.; Carlin, S.; Clardy, S.M.; Keliher, E.J.; Weber, W.A.; Lewis, J.S.; Reiner, T. In Vivo Imaging of GLP-1R with a Targeted Bimodal PET/Fluorescence Imaging Agent. Bioconjugate Chemistry, 2014, 25(7), 1323-1330. doi: 10.1021/bc500178d
  • Graen, T.M.D.; Hoefling, M.; Grubmüller, H. AMBER-DYES: Characterization of Charge Fluctuations and Force Field Parameterization of Fluorescent Dyes for Molecular Dynamics Simulations. Journal of Chemical Theory and Computation, 2014, 10(12), 5505-5512. doi: 10.1021/ct500869p
  • Li, L.-L.; Xu, J.-H.; Qi, G.-B.; Zhao, X.; Yu, F.; Wang, H. Core-Shell Supramolecular Gelatin Nanoparticles for Adaptive and "On-Demand" Antibiotic Delivery. ACS Nano, 2014, 8(5), 4975-4983. doi: 10.1021/nn501040h
  • Viehweger, K.; Barbaro, L.; García, K.P.; Joshi, T.; Geipel, G.; Steinbach, J.; Stephan, H.; Spiccia, L.; Graham, B. EGF Receptor-Targeting Peptide Conjugate Incorporating a Near-IR Fluorescent Dye and a Novel 1,4,7-Triazacyclononane-Based 64Cu(II) Chelator Assembled via Click Chemistry. Bioconjugate Chemistry, 2014, 25(5), 1011-1022. doi: 10.1021/bc5001388
  • Zhou, Z.; Wu, X.; Kresak, A.; Griswold, M.; Lu, Z.-R. Peptide targeted tripod macrocyclic Gd(III) chelates for cancer molecular MRI. Biomaterials, 2013, 34(31), 7683-7693. doi: 10.1016/j.biomaterials.2013.06.057
  • Zou, C.; Loka, R.S.; Zhang, Y.; Cairo, C.W. Glycoform Remodeling Generates a Synthetic T Cell Phenotype. Bioconjugate Chemistry, 2013, 24(6), 907-914. doi: 10.1021/bc300599w
  1. Nakamura, T.; Sugihara, F.; Matsushita, H.; Yoshioka, Y.; Mizukami, S.; Kikuchi, K. Mesoporous silica nanoparticles for 19F magnetic resonance imaging, fluorescence imaging, and drug delivery. Chemical Science, 2015. doi: 10.1039/c4sc03549f
  2. Aldeek, F.; Hawkins, D.; Palomo, V.; Safi, M.; Palui, G.; Dawson, P.E.; Alabugin, I.V.; Mattoussi, H. UV and Sunlight Driven Photoligation of Quantum Dots: Understanding the Photochemical Transformation of the Ligands. Journal of the American Chemical Society, 2015. doi: 10.1021/ja512802x
  3. Hsueh, P.-Y.; Edman, M.C.; Sun, G.; Shi, P.; Xu, S.; Lin, Y.-a.; Cui, H.; Hamm-Alvarez, S.F.; MacKay, J.A. Tear-mediated delivery of nanoparticles through transcytosis of the lacrimal gland. Journal of Controlled Release, 2015. doi: 10.1016/j.jconrel.2014.12.017
  4. Wen, A.M.; Infusino, M.; De Luca, A.; Kernan, D.L.; Czapar, A.E.; Strangi, G.; Steinmetz, N.F. Interface of Physics and Biology: Engineering Virus-Based Nanoparticles for Biophotonics. Bioconjugate Chemistry, 2015, 26(1), 51–62. doi: 10.1021/bc500524f
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