询 价
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. |
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 | 2-8°C |
Expiry | 36 months from the date of manufacture |