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Microarrays have been used to discover an impressive number of clinically informative genomic and pharmacogenomic biomarkers. However, converting promising gene signatures into clinical diagnostic or prognostic tests can be an expensive endeavor with significant development and regulatory risks.
The Genechip System 3000Dx v.2 is the foundation of the Applied Biosystems Clinical Toolkit, which includes cGMP-manufactured microarrays. The Clinical Toolkit provides a proven path to market, enabling test developers to save time and money while helping to reduce regulatory risks.
GeneChip technology has been relied upon by thousands of researchers to obtain reproducible results for all their microarray applications.
Research
Diagnostic test development
Routine testing
GeneChip® System 3000Dx v.2 assay menu | ||
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Application area | RUO* | IVD** |
3’ IVT expression analysis | √ | √ |
Whole-transcript expression analysis | √ | √ |
Genotyping/copy number | √ | |
Cytogenetic analysis | √ | |
Drug metabolism/pharmacogenomics | √ | √ |
miRNA gene regulation | √ | |
Targeted resequencing | √ | |
Custom assays | √ | √ |
* Each “Research Use Only” (RUO) array requires an array-specific Assay Software Module (ASM). A custom ASM can be developed for any GeneChip® Array. A Data Transfer Server (DTS) is required to export .CEL files. ** FDA-cleared, IVD or CE-marked test developed by a third-party company on the GCS 3000Dx platform. |
"In clinical research where irreplaceable human specimens are used, you do not have a second chance. Once you use the sample, it is gone. Thus, it is highly beneficial to use IVD reagents and system with an established good analytical performance."
Catherine Dumur, PhD,
Director of the Molecular Morphology
Genomics Facility and Associate Professor at
Virginia Commonwealth University
"Affymetrix provides the tools to make it easy for Skyline to concentrate on diagnostic content. Building our AMLProfiler test on the FDA-cleared, CE-marked GCS 3000Dx v.2 microarray system using the FDA-cleared, CE-marked Gene Profiling Reagents greatly reduces our regulatory and operational risks, providing a faster path to market."
Henk Viëtor
CEO, Skyline Diagnostics BV
"The need for an FDA-cleared microarray platform was an important consideration in choosing the GCS 3000Dx system for Pathwork’s two FDA-cleared Tissue of Origin (TOO) tests, one that uses FFPE and the other frozen tumor samples."
David Craford
Chief Commercial Officer,
Pathwork Diagnostics
GeneChip Scanner 3000Dx v.2 with AutoLoaderDx | |
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Weight | ~100 lb (45.4 kg) |
Dimensions | 13“ W x 22” D x 18” H (33 cm x 56 cm x 46 cm) |
Loading clearance | 36” (91.4 cm) above laboratory bench Additional 18“ (46 cm) in clearance for AutoloaderDx |
Power | Voltage: 100–240 VAC; Current: 4–2A; Frequency: 50–60 Hz |
GeneChip Fluidics Station 450Dx v.2 | |
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Weight | ~80 lb (36.3 kg) |
Dimensions | 28“ W x 16 1/8” D x 15 13/16” H (71.1 cm x 41 cm x 40.2 cm) |
Loading clearance | Additional 4“ (10.2 cm) at the back for ventilation |
Power | Voltage: 100–240 VAC; Current: 3A; Power: 300 Watts |
Workstation with Affymetrix Molecular Diagnostics Software (AMDS) v1.0 and higher | |
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Weight | Computer monitor – 26 lb (11.8 kg) Computer tower – 43 lb (19.5 kg) |
Dimensions | Computer monitor – 20 ¼“ W x 11” D x 21” H (52 cm x 28 cm x 54 cm) Computer tower – 6 ¾” W x 18 ½“ D x 17 2/3“ H (17 cm x 47 cm x 45 cm) |
Loading clearance | 36” (91.4 cm) above laboratory bench Additional 18“ (46 cm) in clearance for AutoloaderDx |
Power | Voltage: 100–240 VAC |
For In Vitro Diagnostic Use.