Click chemistry describes a class of chemical reactions that use bio-orthogonal or biologically unique moieties to label and detect a molecule of interest in mild, aqueous conditions. The click reaction involves a copper-catalyzed triazole formation from an azide and an alkyne. The azide and alkyne moieties can be used interchangeably; either one can be used to tag the molecule of interest, while the other is used for subsequent detection.
The Andy Fluor™ 555 azide is reactive with terminal alkyne via a copper-catalyzed click reaction that allows the subsequent visualization by fluorescence spectroscopy.
Features
- Efficiency—the click reaction is complete in less than 1 hour;
- Specificity—the reaction between the label and detection tag is selective and specific;
- Stability—the reaction product contains an irreversible, covalent bond;
- Biologically inert—the components of the reaction do not undergo any side reactions.
Figure 1. Click chemistry labeling
Specifications
Label: | Andy Fluor™ 555 | |
Ex/Em: | 553/565 | |
Detection Method: | Fluorescent | |
Solubility: | DMSO, DMF | |
Product Size: | 1 µmol | |
Storage Conditions: | -20 ℃, protect from light | |
Shipping Condition: | Room Temperature | |
Applications Click chemistry labeling |
Datasheet (PDF): | C320 |
Flyer (PDF): | C320 |
Reference
Angew Chem Int Ed Engl (2012) 51:3143-3146
Nucleic Acids Res (2012) 40:e78-e78
Proc Natl Acad Sci U S A (2013) 110:4992-4997
Proc Natl Acad Sci U S A (2007) 104:2614-2619
Angew Chem Int Ed Engl (2009) 48:4030-4033
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