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FITC-Gly-CBT
Nom chimique: N-(2-cyanobenzo[d]thiazol-6-yl)-2-(3-(3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthen]-5-yl)thioureido) acetamide // Synonymes: FITC-glycine-CBT, FITC-glycine-cyanobenzothiazole, FITC-glycine-2-cyanobenzothiazole, CBT-Fluorescein, CBT-Gly-fluoresceine, FG-CBT, FITC-G-CBT, (Cyanobenzothiazolylglycyl-)fluoresceinyl-thiourea, C BT-FITC-thiourea, CBT-FITC-thioharnstoff
- n° Art.:RL-4260
- n° CAS:1207457-29-1
- Formule:C31H19N5O6S2
- Storage temperature:-20°C
- Masse moléculaire:621,64 g/mol
from 200,00 €
description
The site-specific labeling of proteins by chemical reactions has gained increased interest for the investigation of cellular processes. In this regard, the CBT-Cys „click“ condensation reaction has found wide applicability in recent years. The reaction is highly biocompatible and controllable and runs under physiological conditions. It is based on the condensation between an N-terminal L- or D-Cysteine with the cyano group of CBT.
references
A Biocompatible Condensation Reaction for the Labeling of Terminal Cysteine Residues on Proteins; H. Ren, F. Xiao, K. Zhen, Y.P. Kim, H. Xie, Z. Xia, J. Rao; Angew. Chem. Int. Ed. 2009, 48: 9658-9662. https://doi.org/10.1002/anie.200903627
Novel Regioselective Approach to Cyclize Phage-Displayed Peptides in Combination with Epitope-Directed Selection to Identify a Potent Neutralizing Macrocyclic Peptide for SARS-CoV-2; J. T. Hampton, T. J. Lalonde, J. M. Tharp, Y. Kurra, Y. R. Alugubelli, C. M. Roundy, G. L. Hamer, S. Xu, W. R. Liu; ACS Chem. Biol. 2022, 17(10): 2911–2922. https://doi.org/10.1021/acschembio.2c00565
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