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.235delC, c.35insG |
| Sample Type: | gDNA |
| Storage: | Tris-EDTA (10mM Tris-HCl, 1mM EDTA), pH 8.0 |
| Concentration: | 50 ng/μL |
Please submit a detailed description of your project. We will provide you with a customized project plan to meet your research requests. You can also send emails directly to for inquiries.
Please fill out the form below: ×
