| 名稱 | GJB2 p.G4D Reference Standard |
| 型號(hào) | CBPD0023 |
| 報(bào)價(jià) |  |
| 特點(diǎn) | GJB2 p.G4D Reference Standard |
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產(chǎn)品展示 / PRODUCTS
基因檢測(cè)標(biāo)準(zhǔn)品 > 遺傳性耳聾 > CBPD0023GJB2 p.G4D Reference Standard
- 詳細(xì)內(nèi)容
CBPD0023 | |
| Format | Genomic DNA |
| Description | Genetic deafness is a hearing disorder caused by genetic mutations. It is mainly caused by the mutation of mutations in genetic deaf genes and is inherited to descendants. Common deaf genes include GJB2, GJB3, SLC26A4, mitochondrial 12S RRNA, etc. |
| Technical Data | |
| DNA Change | c.11G>A |
| AA Change | p.G4D |
| Zygosity | Homozygous |
| Allelic Frequency | 100% |
| Chr position (GRCh37) | chr13-20763710 |
| Transcript | NM_004004.6 |
| Buffer | Tris-EDTA |
| Product Information | |
| Intended Use | Research Use Only |
| Unit Size | 1ug |
| Concentration | Download for COA |
| Purofication | Download for COA |
| DNA electrophoresis | Download for COA |
| Sanger sequencing |
|
| Storage | 4°C |
| Expiry | 36 months from the date of manufacture |
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