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產(chǎn)品名稱(chēng): Sulfo-Cyanine7 NHS ester
產(chǎn)品型號(hào):
產(chǎn)品展商: 其它品牌
產(chǎn)品文檔: 無(wú)相關(guān)文檔
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
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sigma
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roche
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qiagen
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merck
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millipore
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invitrogen
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life
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ambion
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illumina
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thermo
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ABI
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enzo
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vectorlabs
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chemicon
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Quidel
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peprotech
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cayman
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Biovision
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chondrex
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Meridian
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Kamiya
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Genetex
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Neuromics
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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:
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dark green powder
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Molecular weight:
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827.94
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Molecular formula:
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C41H46N3NaO10S2
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Solubility:
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good in water, DMF, DMSO
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Quality control:
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NMR 1H (95%) and 13C, TLC, functional testing
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Storage conditions:
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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.
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MSDS:
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Download
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Spectral properties
Excitation maximum, nm:
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740
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Extinction coefficient at excitation maximum, Lmol-1cm-1:
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240600
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Emission maximum, nm:
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773
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CF260:
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0.04
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CF280:
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0.04
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Product citations
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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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