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Boc-O2Oc-OH
Chemischer Name: (2-(2-(t-Butyloxycarbonylamino)ethoxy)ethoxy)acetic acid // Synonyme: Boc-AEEA, Boc-Adoa, Boc-Ado, Boc-8-amino-3,6-dioxaoctanoic acid, Boc-PEG-COOH, (2-(2-(Boc-amino)ethoxy)ethoxy)acetic acid
- Art-Nr.:PEG8080
- CAS Nr.:108466-89-3
- Lagertemperatur:-20°C
- Formel:C11H21NO6
- Molare Masse:263,29 g/mol
- Reinheit:min. 98%
Ab 100,00 €
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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