詢  價(jià)
                        
                        
                索取COA
                        
                    產(chǎn)品描述
                    產(chǎn)品數(shù)據(jù)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 | N/A | 
| DNA Change | NM_000463.3 c.-3275T>G | 
| Chr position (GRCh38) | chr2:233757013T>G | 
| Allelic Frequency | 100% | 
| Zygosity | Homozygous | 
| 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 | 
            