Genomics

Sciex GeXP Genetic Analysis System The single best multiplex solution for quantitative, high-throughput, cost-effective gene expression analysis.
Finally, quantitative gene expression that's cost-effective too. The GenomeLab™ GeXP Genetic Analysis System utilizes a patented, highly multiplexed PCR* approach to quickly and efficiently look at the expression of multiplexed gene sets with greater sensitivity and speed. Building on more than a decade of innovative leadership in laboratory automation and capillary electrophoresis technology, the GenomeLab GeXP clears your pathway to discovery.
Multiple applications for gene expression
- Discovery of Gene Targets
- Pathway Analysis
- Biomarker Discovery
- Microarray Data Validation
- RNAi Studies
- Drug Characterization
- Development of Signatures
- Monitor Gene Regulation
The GenomeLab GeXP is flexible enough to adapt to a broad spectrum of applications, yet easily accessible to a wide range of users. This system provides high-quality DNA sequencing and high-precision fragment sizing, with sophisticated software algorithms. The GeXP software automatically analyzes quality and highlights results that need further review, allowing you to rapidly assess and interpret your data.
- De Novo DNA Sequencing
- Heterozygote Detection
- Confirmatory Sequencing
- Mutation Analysis
- Allele Identification
- SNP Scoring
- Microsatellite Instability
- AFLP® Fingerprinting
- Gene Expression
Applications Since the first publication of the DNA double helical structure, electrophoresis has been a standard among the analytical tools used for nucleic acid analysis. Capillary electrophoresis (CE) technology extends the power of electrophoresis by using a format that incorporates direct detection, automation and the ability to study interactions in solution. The following applications are routinely performed on the Beckman Coulter CE-based Genetic analysis systems.
- CEQ™ Series Applications (Capillary array technology)
Dye Terminator Cycle Sequencing
- Automated Heterozygote Detection
- Automated Fragment Sizing and Allele Identification
- Short Tandem Repeat (STR) Analysis
- Single Nucleotide Polymorphisms (SNP)
- Amplified Fragment Length Polymorphisms
- Quantitation / Loss of Heterozygosity
- Automated Generation of Locus Tags - Binning
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