![6-CR6G, SE [6-Carboxyrhodamine 6G, succinimidyl ester] *Single isomer* 详细说明书](/Public/Home/images/pic52.png)
详细说明书![6-CR6G, SE [6-Carboxyrhodamine 6G, succinimidyl ester] *Single isomer* 技术资料](/Public/Home/images/pic53.png)
技术资料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.
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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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| 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 |
| 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 |
