UGT1A1*1/*6 Reference Standard
CBPA0039
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索取COA
产品描述
产品数据库
| 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.G71R |
| DNA Change | NM_000463.3 c.211G>A |
| Chr position (GRCh38) | chr2:233760498G>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 |
