| 名稱 | GJB2 p.G4D Reference Standard |
| 型號 | CBPD0023 |
| 報價 |  |
| 特點 | GJB2 p.G4D Reference Standard |
產(chǎn)品搜索
相關(guān)文章
- AVβ6靶點細(xì)胞篩選模型
- 鑒別出促進(jìn)黑色素瘤進(jìn)展的關(guān)鍵蛋白,開發(fā)出新型癌癥靶向療法
- 老靶點迭代突破創(chuàng)新：Her2靶點細(xì)胞模型
- 一起認(rèn)識下腫瘤細(xì)胞的遷移性
- 腫瘤細(xì)胞內(nèi)的膠原蛋白有哪些作用？
- 【產(chǎn)品推介】LAG-3靶點細(xì)胞篩選模型
- ATCC細(xì)胞株穩(wěn)定整合試驗中的幾個關(guān)鍵因素
- 細(xì)胞株購買以及真假鑒別雜談
- 免疫治療的下一個靶標(biāo)：腫瘤相關(guān)巨噬細(xì)胞？
- 分子診斷標(biāo)準(zhǔn)品，匠心出品，免費申領(lǐng)
聯(lián)系我們
聯(lián)系人：蔣經(jīng)理
電話：4008750250
號碼：
手機：18066071954
地址：南京市棲霞區(qū)緯地路9號
Email： zhangxiangwen@cobioer.com
電話：4008750250
號碼：
手機：18066071954
地址：南京市棲霞區(qū)緯地路9號
Email： zhangxiangwen@cobioer.com
產(chǎn)品展示 / PRODUCTS
基因檢測標(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 |
