Amersham CyDye DIGE Fluor Cy3 minimal dye, 5 nmol
Allow detection of up to three prelabeled protein samples and standards on the same 2D electrophoresis gel.
Size and chargematched dyes enable comigration of labeled samples within the gel.
Bright and highly sensitive dyes allow the use of the minimal labeling technique.
Minimal loss of signal during labeling, separation, and scanning.
No change in signal over wide pH range used during firstdimension (IEF) separation.
Discrete signal from each fluor with minimal crosstalk contributes to high accuracy.
CyDye DIGE fluors are available as minimal and saturation labeling dyes. The minimal dyes are intended for general 2D application use where sufficient amounts of sample are available. The saturation dyes from the Scarce Sample Labeling Kit are designed to be used for applications where only small amounts of sample are available, for example in Laser Capture Microdissection. In total, three minimal dyes and two saturation dyes are available.
CyDye DIGE fluors are exceptional dyes for multicolor analysis, offering bright and intense colors with narrow excitation and emission bands. The fluors are spectrally distinct, making them highly suitable for multicolor detection. CyDye DIGE fluors utilize these benefits but are also size and chargematched specifically for 2D DIGE using Ettan DIGE system.
CyDye DIGE Fluor Minimal DyesProtein samples and the internal standard are each labeled with one CyDye DIGE Fluor minimal dye. These labeled samples are then combined, run on an isoelectric focusing gel in the first dimension, and separated by SDSPAGE in the second dimension. Electrophoresis is simplified with Ettan IPGphor 3, or Multiphor II with Immobiline DryStrip gels in the first dimension and Ettan DALTtwelve or Ettan DALTsix electrophoresis systems in the second dimension. The ability to multiplex different CyDye DIGE Fluor minimal dyelabeled samples on the same gel means that the different samples will be subjected to exactly the same first and seconddimension running conditions. Consequently, the same protein labeled with any of the CyDye DIGE Fluor minimal dyes and separated on the same gel will migrate to the same position on the 2D gel and overlay. This limits experimental variation and ensures accurate withingel matching.