The Spectrum Compact CE System is an integrated and efficient instrument that brings you the independence to perform Sanger sequencing and fragment analysis in your laboratory, under your control, and at your convenience.
It is designed for use with existing sequencing chemistries using fluorescently labeled dideoxynucleotide triphosphate and 4-, 5- and 6-dye STR kits from Promega and other commercially available kits.
An Affordable Benchtop Instrument for Sanger Sequencing and Fragment Analysis
- Single base resolution
- Integrated touchscreen operation
- 6-dye-compatible CE analysis
One Compact System Optimized For a Broad Range of Applications
- De novo sequencing
- NGS confirmation
- Mutation detection
- Mitochondrial sequencing
- PCR sizing
- SNP genotyping
Small-Footprint Advanced Multiplexing
Electropherogram of 1ng of 2800 control DNA analyzed with PowerPlex® Fusion 6C System run on prototype Spectrum Compact CE System. Injection was performed at 1.2 kV for 8 seconds as a GeneMarker®, Mutation Surveyor® and GeneMapper®. Image credit: Promega
Spectrum Compact Achieves a 1bp resolution as can be seen in the D1S1656 and D2S441 loci in the PowerPlex® Fusion 6C System Allelic Ladder. Injection was performed at 1.2 kV for 8 seconds. Image credit: Promega
Accurate and Fast Sequencing
Representative portion of an electropherogram (Top Panel) generated using the Applied Biosystems BigDye® v3.1 Kit, Polymer 7 and Hitachi base calling software; (Bottom Panel) whole data file. Image credit: Promega
Integrated Touchscreen Operation
The Spectrum Compact Control Software provides a simple user interface with a clear display of useful features including run set up, consumables and array usage information, as well as system maintenance reminders.
Image credit: Promega
With the easy to use operational workflow instrument, the instrument also offers the ability to monitor run progress and view results while a run is in progress. Export files are compatible with commercially available data analysis software such as GeneMarker®, Mutation Surveyor® and GeneMapper®.