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腫瘤早篩甲基化標(biāo)準(zhǔn)品
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診斷試劑
diagnosis
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 | 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 |