ClearSeq Cardiomyopathy
ClearSeq 心肌相關病變基因研究
ClearSeq Cardiomyopathy is a next generation sequencing target enrichment panel designed specifically for inherited forms of cardiomyopathy. Following a careful review of cardiomyopathy publications as well as information available from GeneReviews, an NIH online resource, 34 genes known to be associated with hypertrophic cardiomyopathy, dilated cardiomyopathy, and arrythmogenic right ventricular cardiomyopathy have been included.Compatible with HaloPlexHS and HaloPlex Target Enrichment Systems
ClearSeq Cancer
Designed specifically for inherited forms of cardiomyopathy including hypertrophic, dilated and rightCompatible with HaloPlexHS and HaloPlex
產品列表
| 貨號 | 產品 | 數量 | |
|---|---|---|---|
| G9943A | ClearSeq Cardiomyopathy, HS, ILM | 16 rxns | |
| G9943B | ClearSeq Cardiomyopathy, HS, ILM | 96 rxns | |
| G9908A | ClearSeq Cardiomyopathy, ILM | 16 rxns | |
| G9908B | ClearSeq Cardiomyopathy, ILM | 96 rxns | |
| G9944A | ClearSeq Cardiomyopathy, HS, ION | 16 rxns | |
| G9944B | ClearSeq Cardiomyopathy, HS, ION | 96 rxns | |
| G9909A | ClearSeq Cardiomyopathy, ION | 16 rxns | |
| G9909B | ClearSeq Cardiomyopathy, ION | 96 rxns |
ClearSeq Cardiomyopathy
- Expert-optimized content - Highly targeted content enabling analysis of regions implicated in rare disease pathogenesis
- Fast track to answers - Proven, high-performing capture oligos are coupled with highly efficient SureSelect and HaloPlex workflows, providing faster time to results and compatibility with samples of limited availability (high throughput or benchtop sequencers)
- Comprehensive Workflow Solution - Accelerated sample to categorized variants with SureCall
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