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.
|
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.
| name | 6-cr6g, se [6-carboxyrhodamine 6g, succinimidyl ester] *single isomer* | ||
|---|---|---|---|
| cat# | 342-5 mg | cas# | |
| storage# | −20°c desiccated and minimize light exposure | shelf life# | 12months |
| 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 desiccated and minimize light exposure |
| shelf life# | 12months |
| ex(nm)# | 524 |
| em(nm)# | 551 |
| mw# | 555.59 |
| solvent# | dmso |