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重要文件

SDS

COO/COA

OCY302
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花菁素Cy3琥珀酰亚胺酯
适用于 HPLC, ≥95%
别名: Cy3-NHS
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包装规格 商品货号 库存 价格 数量
1mg OCY302-1mg ¥145.00
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5mg OCY302-5mg ¥389.00
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10mg OCY302-10mg ¥580.00
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25mg OCY302-25mg ¥1168.00
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50mg OCY302-50mg ¥1930.00
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产品信息
常规属性
其他属性
描述
安全信息
产品信息
CAS Number 1032678-38-8
Linear Formula

C34H40ClN3O4

Molecular weight 590.16
Beilstein
EC Number

MDL Number

PubChem CID 121226457
PubChem SID 517723047
常规属性
Purity 95%
Appearance Red powder
Solubility Freely soluble in methanol, chloroform, DMSO, DMF, and other organic solvents; insoluble in water.
Purity Testing Method HPLC
Structural Identification Method NMR/MS
Storage Conditions −20 °C, keep in dark place.
其它属性
Spectral Properties
Excitation Wavelength (λₑₓ) 555 nm
Emission Wavelength (λₑₘ) 570 nm
Molar Extinction Coefficient (ε) 149000 L·mol⁻¹·cm⁻¹
说明
安全信息
  • Symbol GHS

  • 危险代码

  • 风险声明

  • 安全声明

  • RIDADR

  • WGK Germany

  • RTECS

  • F

  • 危险性类别

  • 包装等级

  • HS Code

  • 毒性

  • Autoignition Temperature

相关产品
引用文献
1. Yang, J.; Zhang, R.; Radford, D.C.; Kope?ek, J. FRET-trackable biodegradable HPMA copolymer-epirubicin conjugates for ovarian carcinoma therapy. Journal of Controlled Release, 2015, 218, 36–44. doi: 10.1016/j.jconrel.2015.09.045
2. Albertazzi, L.; van der Veeken, N.; Baker, M.B.; Palmans, A.R.A.; Meijer, E.W. Supramolecular copolymers with stimuli-responsive sequence control. Chemical Communications, 2015, 51(90), 16166–16168. doi: 10.1039/c5cc06951c
3. Koo, H.; Choi, M.; Kim, E.; Hahn, S.K.; Weissleder, R.; Yun, S.H. Bioorthogonal Click Chemistry-Based Synthetic Cell Glue. Small, 2015, 11(48), 6458–6466. doi: 10.1002/smll.201502972
4. Poongavanam, M.-V.; Kisley, L.; Kourentzi, K.; Landes, C.F.; Willson, C. Ensemble and Single-Molecule Biophysical Characterization of D17.4 DNA Aptamer-IgE Interactions. Biochimica et Biophysica Acta, 2016, 1864(1), 154–164. doi: 10.1016/j.bbapap.2015.08.008
5. Kijima, S.T.; Hirose, K.; Kong, S.-G.; Wada, M.; Uyeda, T.Q.P. Distinct Biochemical Properties of Arabidopsis thaliana Actin Isoforms. Plant and Cell Physiology, 2016, 57(1), 46–56. doi: 10.1093/pcp/pcv176
6. Leenders, J.; Baker, M.B.; Pijpers, I.; Lafleur, R.; Albertazzi, L.; Palmans, A.R.A.; Meijer, E.W. Supramolecular polymerisation in water; elucidating the role of hydrophobic and hydrogen-bond interactions. Soft Matter, 2016, 12, 2887–2893. doi: 10.1039/c5sm02843d
7. Hartley, J.M.; Zhang, R.; Gudheti, M.; Yang, J.; Kope?ek, J. Tracking and quantifying polymer therapeutic distribution on a cellular level using 3D dSTORM. Journal of Controlled Release, 2016, 231, 50–59. doi: 10.1016/j.jconrel.2016.02.005
8. Ray, J.; Shin, I.; Ilgu, M.; Bendickson, L.; Gupta, V.; Kraus, G.A.; Nilsen-Hamilton, M. IMAGEtags: Quantifying mRNA Transcription in Real Time with Multiaptamer Reporters. Methods in Enzymology, 2016, 572, 193–213. doi: 10.1016/bs.mie.2016.02.028
9. Zhong, Q.; Merkel, O.M.; Reineke, J.J.; da Rocha, S.R.P. Effect of the Route of Administration and PEGylation of Poly(amidoamine) Dendrimers on their Systemic and Lung Cellular Biodistribution. Molecular Pharmaceutics, 2016, 13(6), 1866–1878. doi: 10.1021/acs.molpharmaceut.6b00036
10. Wang, C.; Tang, F.; Wang, X.; Li, L. Synthesis and application of biocompatible gold core-poly-(L-Lysine) shell nanoparticles. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2016, 506, 425–430. doi: 10.1016/j.colsurfa.2016.07.014
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