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重要文件

SDS

COO/COA

OCY302

花菁素Cy3琥珀酰亚胺酯

Name: 花菁素Cy3琥珀酰亚胺酯
Brand: OmiChem
SKU: OCY302
Availability: InStock

适用于 HPLC, ≥95%

别名: Cy3-NHS

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选择规格

包装规格	商品货号	库存	价格	数量
1mg	OCY302-1mg	有库存	¥145.00	- +
5mg	OCY302-5mg	有库存	¥389.00	- +
10mg	OCY302-10mg	有库存	¥580.00	- +
25mg	OCY302-25mg	有库存	¥1168.00	- +
50mg	OCY302-50mg	有库存	¥1930.00	- +

申请批量订单加入购物车

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

Cyanine3 NHS酯是一种反应性染料，用于高效胺偶联，与蛋白质、肽和其他生物分子形成稳定的酰胺键。这种非磺化试剂具有优异的有机溶解度和高标记效率。NHS酯基团确保在pH 7-9条件下与伯胺快速、选择性反应。适用于生物成像、免疫测定和分子探针中的荧光标记。
对于水相应用，请考虑磺基-Cyanine3 NHS酯，它提供增强的水溶性。请在-20°C干燥保存，避光防潮。

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

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

重要文件

OCY302

花菁素Cy3琥珀酰亚胺酯

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

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

分子化学

仅适用于全价商品。在线独家。

提交电子邮件即表示您同意：

接收OMICHEM的促销邮件（随时取消订阅）

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重要文件

OCY302

花菁素Cy3琥珀酰亚胺酯

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

OCY311

花菁素Cy3顺环辛烯

OCY310

花菁素Cy3巯基

OCY309

花菁素Cy3氨基

OCY308

花菁素Cy3氰基苯并噻唑

OCY307

花菁素Cy3环辛炔

OCY306

花菁素Cy3炔基

OCY305

花菁素Cy3叠氮

OCY304

花菁素Cy3四嗪

OCY303

花菁素Cy3马来酰亚胺

OCY301

花菁染料Cy3羧酸

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

分子化学

仅适用于全价商品。在线独家。

提交电子邮件即表示您同意：

接收OMICHEM的促销邮件（随时取消订阅）

我们的使用条款（包括仲裁条款）

根据我们的隐私政策与服务提供商共享数据