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Sulfo-Cyanine7 NHS ester

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產(chǎn)品名稱(chēng): Sulfo-Cyanine7 NHS ester
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簡(jiǎn)單介紹

訂購(gòu)貨號(hào) 產(chǎn)品名稱(chēng)及規(guī)格 價(jià)格(¥)15320 Sulfo-Cyanine7 NHS ester, 1 mg 2080.0025320 Sulfo-Cyanine7 NHS ester, 5 mg 5330.0045320 Sulfo-Cyanine7 NHS ester, 25 mg 11050.0055320 Sulfo-Cyanine7 NHS ester, 50 mg 19500.0065320 Sulfo-Cyanine7 NHS ester, 100 mg 31850.00


Sulfo-Cyanine7 NHS ester  的詳細(xì)介紹
abcam sigma roche qiagen merck millipore
invitrogen life ambion illumina thermo ABI
enzo vectorlabs chemicon Quidel peprotech cayman
Biovision chondrex Meridian Kamiya Genetex Neuromics

訂購(gòu)貨號(hào) 產(chǎn)品名稱(chēng)及規(guī)格 價(jià)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


水溶近紅外染料sulfo-Cyanine7,是胺類(lèi)活性琥珀酸亞胺酯。


Sulfo-Cyanine7是Cy7®熒光團(tuán)的的改良衍生物,量子產(chǎn)率提高20%,并具有更好的耐光性。該染料尤其適用于NIR成像應(yīng)用。


近紅外熒光染料利用了生物組織在特定的波長(zhǎng)范圍里的透明度。這種方法是無(wú)損傷性的,并允許在活體內(nèi)對(duì)多種已標(biāo)記的生物分子的分布進(jìn)行跟蹤。


Sulfo-Cyanine7 NHS ester可以很輕松的標(biāo)記生物分子,如:蛋白質(zhì)。標(biāo)記的分子可以用于后續(xù)多種研究及**開(kāi)發(fā)相關(guān)的實(shí)驗(yàn)。


這種染料有很高的水溶解度,尤其適用于痕量蛋白質(zhì)和易變性蛋白質(zhì)的標(biāo)記。需有機(jī)溶劑才能溶解的非磺化的Cyanine7 NHS ester。

推薦手冊(cè):

氨基分子的NHS酯標(biāo)記

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 for19F 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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