Details
| Product Infomation | |
|---|---|
| Product Description: | Deafness is a common clinical condition and is caused by hereditary factors in about 50% of cases. Its main modes of inheritance are autosomal recessive, autosomal dominant, sex-linked and mitochondrial. The four deafness-related genes commonly found in Chinese are GJB2, GJB3, SLC26A4, and mitochondrial 12S rRNA, and the deafness caused by these four genes accounts for about 80% of the overall genetic deafness. Currently, the clinical methods used for deafness gene mutation detection include fluorescence polymerase chain reaction (PCR), gene chip hybridization, Sanger sequencing, and second generation sequencing. |
| Features: | Mutaiton: c.281C>T, c.589G > A, c.919-2A >G, c.1174A > T, c.1229C > T, c.IVS15 + 5G >A, c.2027T > A, c.2168A > G. |
| Sample Type: | gDNA |
| Storage: | Tris-EDTA (10mM Tris-HCl, 1mM EDTA), pH 8.0 |
| Concentration: | 50 ng/μL |
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