UGT1A1*27 Reference Standard
CBPA0093
詢 價
索取COA
產品描述
產品數據庫
| Introduction | |
| 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. Among its related pathways are Glucose / Energy Metabolism and Statin Pathway - Generalized, Pharmacokinetics. |
| Technical Data | |
| Gene | UGT1A1 |
| AA Change | p.P229Q |
| DNA Change | NM_000463.3 c.686C>A |
| Chr position (GRCh38) | chr2:233760973C>A |
| 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 | 2-8°C |
| Expiry | 36 months from the date of manufacture |
