中文 | EN
6-CR6G, SE [6-Carboxyrhodamine 6G, succinimidyl ester] *Single isomer*
In general, rhodamine 6G conjugates have higher fluorescence quantum yields than tetramethylrhodamine conjugates, as well as good photostability.
6-CR6G, SE [6-Carboxyrhodamine 6G, succinimidyl ester]
|
Cat# |
Size |
Price |
MW |
Abs |
Em |
Soluble in |
Storage |
|
342 |
5 mg |
¥1750 |
555.59 |
524 nm |
551 nm |
DMSO |
4 oC and desiccated |
|
|
Features and Biological Applications6-CR6G, SE is amine-reactive derivative of of 6-CR6G. It is preferred for some complicated biological applications where reproducibility is more critical than material cost since the minor positional difference between 5-CR6G and 6-CR6G might significantly affect some biological properties of the underlying conjugates. In general, rhodamine 6G conjugates have higher fluorescence quantum yields than tetramethylrhodamine conjugates, as well as good photostability.
|
References
1. Hung SC, et al. (1997). Optimization of spectroscopic and electrophoretic properties of energy transfer primers. Anal Biochem252, 78-88.
2. Hung SC, et al. (1996). Energy transfer primers with 5- or 6-carboxyrhodamine-6G as acceptor chromophores. Anal Biochem238, 165-70.
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Description
| Name | 6-CR6G, SE [6-Carboxyrhodamine 6G, succinimidyl ester] *Single isomer* | ||
|---|---|---|---|
| CAT# | 342-5 mg | CAS# | |
| Storage# | -20°C Sealed & desiccated & Minimized light exposure | Shelf Life# | 24 months |
| Ex(nm)# | 524 | Em(nm)# | 551 |
| MW# | 555.59 | Solvent# | DMSO |
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