ACCUiN Next Generation Deafness Gene Hotspot Panel
GJB2, GJB3, GJB6 complete coding regions and OTOF, SLC16A4, and mitochondrial gene hotspots
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ACCUiN Next Generation Deafness Gene Hotspot Panel
Product Introduction
ACCUiN Next Generation Deafness Gene Hotspot Panel is a qualitative detection designed using Multiplex polymerase chain reaction (Multiplex PCR), requiring next-generation sequencing system (NGS) to detect whether test samples have mutations in specific regions of GJB2, GJB3, GJB6, OTOF, SLC16A4, and mitochondrial genes. ACCUiN Next Generation Deafness Gene Hotspot Panel can be used to detect single nucleotide variants (SNVs), multi-nucleotide variants (MNVs), insertions, deletions, or insertion/deletion (INDELs) variants in specific regions of human GJB2 (NM_004004), GJB3 (NM_024009), GJB6 (NM_001110219), OTOF (NM_194248), SLC16A4 (NM_000441), and mitochondrial (mtDNA) genes. ACCUiN Next Generation Deafness Gene Hotspot Panel has passed quality validation and functional verification to ensure performance stability and reproducibility. ACCUiN Next Generation Deafness Gene Hotspot Panel can provide at least 48 detection reactions.
Specifications
- DFN-48A: Index 1-24
- DFN-48B: Index 25-48
- DFN-48C: Index 49-72
- DFN-48D: Index 73-96
- Reaction quantity: 48 reactions
- Detection target: GJB2, GJB3, GJB6 complete coding regions and OTOF, SLC16A4, and mitochondrial gene hotspots
- Detection method: Multiplex PCR + NGS
- Sample type: Whole blood, saliva
Simple Flowchart
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