UGT1A1*27 Reference Standard

CBPA0093

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. Among its related pathways are Glucose / Energy Metabolism and Statin Pathway - Generalized, Pharmacokinetics.

Technical Data
Gene	UGT1A1
AA Change	p.P229Q
DNA Change	NM_000463.3 c.686C>A
Chr position (GRCh38)	chr2:233760973C>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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诊断标准品联系方式：华东销售经理：15000320447 华北销售经理：18628311252 华南销售经理：13823536064 华中&华西销售经理：18071545918 华中&西南销售经理：13871580511 全国销售经理：13816461235

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