6-TAMRA BCN
6-TAMRA BCN is a derivative of TAMRA (tetramethylrhodamine) featuring a BCN (bicyclo[6.1.0]nonyne) group, designed for copper-free click chemistry reactions. 6-TAMRA BCN is primarily used for copper-free click chemistry-based bioconjugation (Ex/Em = 553/576 nm).
For research use only. We do not sell to patients.
- Formula: C46H56N4O9
- Molecular Weight:808.96
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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 808.96
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Formula C46H56N4O9
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SMILES
O=C(NCCCOCCOCCOCCCNC(OC[C@H]1[C@@]2(CCC#CCC[C@]12[H])[H])=O)C3=CC=C(C(O4)=O)C(C54C(C=CC(N(C)C)=C6)=C6OC7=C5C=CC(N(C)C)=C7)=C3
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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)