ClearSeq Connective Tissue Disorder
ClearSeq 結締組織異常分析
ClearSeq Connective Tissue Disorder focuses on inherited forms of connective tissue disorders, specifically targeting genetic variations associated with Marfan syndrome, Ehlers-Danlos syndrome, Loeys-Dietz syndrome, thoracic aortic aneurysm and dissection (TAAD), Stickler syndrome, Osteogenesis imperfecta and other related disorders.Compatible with HaloPlexHS and HaloPlex Target Enrichment Systems
ClearSeq Connective Tissue Disorders
Focus on 40 genes known to play an important role in inherited forms of connective tissue disorder including Marfan syndrome, Ehlers-Danlos syndrome, Loeys-Dietz syndrome, thoracic aortic aneurysm and dissection (TAAD), Stickler syndrome and Osteogenesis imperfectaCompatible with HaloPlex
產品列表
| 貨號 | 產品 | 數量 | |
|---|---|---|---|
| G9954C | ClearSeq Made-to-Order Panels, HS | 48 rxns | |
| G9954B | ClearSeq Made-to-Order Panels, HS | 96 rxns | |
| G9953C | ClearSeq Made-to-Order Panels | 48 rxns | |
| G9953B | ClearSeq Made-to-Order Panels | 96 rxns |
ClearSeq Connective Tissue Disorder
- 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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