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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

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