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Have you ever wondered if the differences you see in protein abundance are real? Ever wished you could have greater confidence in your 2-D results, so that you know you are concentrating on biologically relevant proteins, without worrying about reproducibility? Well, stop wondering. Now you know.
With Ettan DIGE System you can be confident that changes in protein abundance are real
Ettan™ DIGE System, 2-D Fluorescence Difference Gel Electrophoresis, ensures that each protein spot has its own internal standard. This is the only effective way to remove gel to gel variation, thereby significantly increasing accuracy and reproducibility.
Ettan DIGE System uses size and charge-matched, spectrally resolvable CyDye™ fluors, simultaneously separating up to three samples on a single 2-D gel. After 2-D electrophoresis and scanning on Typhoon™ Variable Mode Imager, DeCyder™ Differential Analysis Software automatically locates and analyzes protein spots, assigning statistical confidence to each and every difference. All within minutes.
Click here for an Introduction to Ettan DIGE System |  |
