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地址：北京市海淀区西幼口路66号中关村东升科技园C-1楼三层
Azide PEG Amine, TFA Salt
产品代号：
AZIDE-PEG-NH2TFA
产品纯度：
≥ 95%
包装规格：
1g, 10g, 100g等（特殊包装需收取分装用度）
分子量：
3500 Da, 5000 Da等
关键词：
科研客户幼批量一键采购地址（幼于5克）
- 产品描述
- 参考文件
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welcome-球速体育科技提供高品质叠氮聚乙二醇胺三氟乙酸盐 ，产品取代率≥95%。
welcome-球速体育科技出产的异双职能叠氮化物PEG胺产品通常用作两种分歧化学物质的交联剂或距离物。此异职能PEG衍生物中的PEG部门可提供水溶性、生物相容性及柔性。此产品专门利用于抗体偶联药物(ADC’s)的开发。
产品编码
产品代号
A5191
AZIDE-PEG2000-NH2TFA
A5238
AZIDE-PEG3500-NH2TFA
A5239
AZIDE-PEG5000-NH2TFA
A5310
AZIDE-PEG7500-NH2TFA
welcome-球速体育科技提供AZIDE-PEG-NH2TFA分子量3500 Da, 5000 Da的产品1克和10克包装。
welcome-球速体育科技提供分装服务 ，必要收取分装用度 ，若是您必要分装为其他规格请与我们联系。
welcome-球速体育科技同时提供其他分子量的AZIDE-PEG-NH2TFA衍生物产品 ，如你必要请与我司sales@jenkem.com联系。
welcome-球速体育科技提供大批量出产产品及GMP级别产品 ，如需报价请与我们联系。
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References:
1. Coppock, M.B., et al., A novel discovery, maturation, and assay integration approach for the development of ruggedized multi-valent capture receptors exemplified against the chikungunya virus E2 protein, Sensing and Bio-Sensing Research, 2019, V. 22.
2. Sun, T., et al., A targeting theranostics nanomedicine as an alternative approach for hyperthermia perfusion, Biomaterials, 2018.
3. Yu, S., et al., A density gradient of VAPG peptides on a cell-resisting surface achieves selective adhesion and directional migration of smooth muscle cells over fibroblasts. Acta biomaterialia, 2018, 72, pp.70-81.
4. Ma, H., et al., Dehydroascorbic Acid and pGPMA Dual Modified pH-Sensitive Polymeric Micelles for Target Treatment of Liver Cancer, Journal of pharmaceutical sciences, 2018, 107(2), pp.595-603.
5. Ma, H., DHA and pGPMA Dual Modified pH Sensitive Polymeric Micelles for Target Treatment of Liver Cancer, Journal of Pharmaceutical Sciences, 2017.
6. Pei, X., et al., Dehydroascorbic Acids-modified Polymer Micelles Target Cancer Cells to Enhance Anti-tumor Efficacy of Paclitaxel. Scientific Reports, 2017, 7(1):975.
7. Ackerman, D.S., et al., Tethered fluorogen assay to visualize membrane apposition in living cells, Bioconjugate Chemistry, 2017.
8. Zhou, X., et al., d‐Fructose Modification Enhanced Internalization of Mixed Micelles in Breast Cancer Cells via GLUT5 Transporters, Macromolecular Bioscience, 2017.
9. Guo, Y., et al., Cell Microenvironment-Controlled Antitumor Drug Releasing-Nanomicelles for GLUT1-Targeting Hepatocellular Carcinoma Therapy, ACS Applied Materials and Interfaces, 2015.
10.Sun, T., et al., Co-delivery of Cu(I) chelator and chemotherapeutics as a new strategy for tumor theranostic, Journal of Controlled Release, 2020, V. 321, P. 483-496.
11.Mertgen, A.S., et al., A low-fouling, self-assembled, graft co-polymer and covalent surface coating for controlled immobilization of biologically active moieties, Applied Surface Science, 2022.
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