| 名稱 | UGT1A1*80 Reference Standard |
| 型號 | CBPA0069 |
| 報價 |  |
| 特點 | UGT1A1*80 Reference Standard |
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產(chǎn)品展示 / PRODUCTS
基因檢測標(biāo)準(zhǔn)品 > 用藥指導(dǎo) > CBPA0069UGT1A1*80 Reference Standard
- 詳細(xì)內(nèi)容
| CBPA0069 | |
| Format | Genomic DNA |
| Description | UGT1A1 (UDP Glucuronosyltransferase Family 1 Member A1) is a Protein Coding gene. Diseases associated with UGT1A1 include Crigler-Najjar Syndrome, Type I and Crigler-Najjar Syndrome, Type Ii. |
| Technical Data | |
| Gene | UGT1A1 |
| AA Change | N/A |
| DNA Change | N/A |
| Chr position (GRCh38) | chr2 NC_000002.12:g.233759924C>T |
| Allelic Frequency | 50% |
| Zygosity | Heterozygous |
| 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 |
