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Boc-O2Oc-OH
Nom chimique: (2-(2-(t-Butyloxycarbonylamino)ethoxy)ethoxy)acetic acid // Synonymes: Boc-AEEA, Boc-Adoa, Boc-Ado, Boc-8-amino-3,6-dioxaoctanoic acid, Boc-PEG-COOH, (2-(2-(Boc-amino)ethoxy)ethoxy)acetic acid
- n° Art.:PEG8080
- n° CAS:108466-89-3
- Formule:C11H21NO6
- Storage temperature:-20°C
- Masse moléculaire:263,29 g/mol
- Pureté:min. 98%
from 75,00 €
description
Boc-AEEA is used as a spacer and hydrophilic linker for attachment of proteins and other biomolecules to various targets.
references
HaloTag Protein-Mediated Site‐Specific Conjugation of Bioluminescent Proteins to Quantum Dots. Yan Zhang, Min‐kyung So, Andreas M. Loening, Hequan Yao, Sanjiv S. Gambhir, Jianghong Rao; Angew. Chem. Int. Ed. 2006; 45(30): 4936-4940. DOI:10.1002/anie.200601197.
A Biocompatible Condensation Reaction for the Labeling of Terminal Cysteine Residues on Proteins. Hongjun Ren, Fei Xiao, Ke Zhan, Young‐Pil Kim, Hexin Xie, Zuyong Xia, Jianghong Rao; Angew. Chem. Int. Ed. 2009; 48(51): 9658-9662, DOI:10.1002/anie.200903627.
Effects of Neighboring Glycans on Antibody–Carbohydrate Interaction. Chi‐Hui Liang, Sheng‐Kai Wang, Chin‐Wei Lin, Cheng‐Chi Wang, Chi‐Huey Wong, Chung‐Yi Wu; Angew. Chem. Int. Ed. 2011; 50(7): 1608-1612. DOI:10.1002/anie.201003482.
Sulphated hyaluronic acids functionalised with dopamine. Guarise, Cristian; Pluda, Stefano; Galesso, Devis; PCT Int. Appl. 2018; WO 2018092013 A1.
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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