6-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.

Product description

Ex(nm) : 524

Em(nm) : 551

Solvent：DMSO

MW : 555.59

Features and Biological Applications

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.

规格

英文名称

6-Carboxyrhodamine 6G, succinimidyl ester（Single isomer）

储存条件

避光,-20°C储存,干燥

运输条件

超低温运输

名称和识别符

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小分子

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化学和物理性质

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对光和湿度敏感

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