5-JOE azide, CHC protected
5-JOE azide, CHC-protected, is a derivative of JOE. It features an azide group for use in click chemistry reactions (CuAAC) and a CHC (cyclohexylcarbodiimide) protecting group for stable oligonucleotide synthesis. 5-JOE azide, CHC-protected, is suitable for click chemistry-based bioconjugation (Ex/Em = 520/548 nm) .
For research use only. We do not sell to patients.
- Formula: C40H40Cl2N4O10
- Molecular Weight:807.67
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
Chemical Information
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Molecular Weight 807.67
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Formula C40H40Cl2N4O10
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SMILES
[N-]=[N+]=NCCCNC(C1=CC=C(C(C(O2)=O)=C1)C32C(C=C4OC)=C(C(Cl)=C4OC(C5CCCCC5)=O)OC6=C3C=C(OC)C(OC(C7CCCCC7)=O)=C6Cl)=O
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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EdU Incorporation Assay (Click Chemistry-Based DNA Synthesis Measurement)
The EdU incorporation assay measures DNA synthesis by adding the thymidine analog 5-ethynyl-2′-deoxyuridine to cells or tissues, where it is incorporated into newly synthesized DNA during S phase. Incorporated EdU is detected by copper-catalyzed azide-alkyne cycloaddition, in which a fluorescent azide covalently reacts with the ethynyl group on EdU, allowing S-phase cells to be detected by fluorescence microscopy, flow cytometry, or high-content imaging. EdU detection does not require DNA denaturation or anti-BrdU antibody access, which preserves sample structure and improves compatibility with immunostaining and multiparameter cytometry compared with BrdU-based detection. EdU can be cytotoxic in a cell-type- and exposure-dependent manner, so pulse duration, concentration, and continuous-labeling designs should be validated for each cell type.
Purity & Documentation
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)