The Amersham CyDye DIGE Cy2 Minimal Dye, 5 nmol (25801082) is a Cy2 minimal fluorescent dye for 2-D Fluorescence Difference Gel Electrophoresis protein analysis. This 5 nmol Amersham CyDye DIGE Fluor is designed for detecting protein abundance differences using minimal labelling in Ettan DIGE system workflows.
Key Features
- Cy2 minimal dye format, matching the verified 25801082 Amersham CyDye DIGE Fluor variant
- 5 nmol dye quantity, supplied as the individual Cy2 minimal dye pack size
- Designed for 2-D DIGE, supporting detection of protein abundance differences in fluorescence difference gel electrophoresis
- Size and charge-matched dye design, enabling co-migration of labelled samples within the same 2-D gel
- Multicolour analysis support, allowing up to three prelabelled protein samples and standards on one 2-D electrophoresis gel
- Bright, highly sensitive fluorescence, supporting the minimal labelling technique
- Low crosstalk signal behaviour, helping improve accuracy when using spectrally distinct DIGE fluors
- General 2-D application use, intended for workflows where sufficient sample amounts are available
Benefits
- Helps compare protein abundance differences while reducing gel-to-gel variation through same-gel multiplexing.
- Supports accurate within-gel matching because the same protein labelled with different minimal dyes migrates to the same position.
- Enables efficient 2-D DIGE workflows where Cy2 is required as one of the spectrally distinct fluorescent dyes.
- Supports reliable signal detection through bright fluorescence and minimal signal loss during labelling, separation and scanning.
- Provides the exact 5 nmol Cy2 minimal dye variant for laboratories using Amersham CyDye DIGE Fluors.
Why Choose the Amersham CyDye DIGE Cy2 Minimal Dye, 5 nmol (25801082)?
The Amersham CyDye DIGE Cy2 Minimal Dye, 5 nmol (25801082) is a specific Cytiva Amersham reagent for 2-D DIGE protein abundance analysis. John Morris Group can help Australian laboratories source the correct Amersham CyDye DIGE Fluor for Ettan DIGE system workflows, minimal labelling and comparative protein analysis.
