6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer), 6-CR6G, SE,6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer),

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

有货

6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer), 6-CR6G, SE,6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer),

品牌:Jinpan
6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer)

MSDS

质检证书(CoA)

相似产品

货号 (SKU) 包装规格 是否现货 价格 数量
C273250-5mg 5mg 期货 6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer), 6-CR6G, SE,6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer),  

基本信息

产品名称 6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer)
英文名称 6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer)
别名 6-CR6G, SE
英文别名 6-CR6G, SE
运输条件 超低温冰袋运输

一般描述

Product description

Ex(nm) : 524

Em(nm) : 551

Solvent:DMSO

MW : 555.59

6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer), 6-CR6G, SE,6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer),
Features and Biological Applications

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

6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer), 6-CR6G, SE,6-Carboxyrhodamine 6G, succinimidyl ester(Single isomer),
Features and Biological Applications

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.

相关属性

敏感性 对光和湿度敏感
储存温度 避光,-20°C储存,干燥
品牌 Jinpan