SLCO1B1*14 Reference Standard

CBPA0123

询价

索取COA

产品描述

产品数据库

Introduction
Format	Genomic DNA
Description	SLCO1B1 (Solute Carrier Organic Anion Transporter Family Member 1B1) is a Protein Coding gene. Diseases associated with SLCO1B1 include Hyperbilirubinemia, Rotor Type and Gilbert Syndrome.

Technical Data
Mutation 1	Gene: SLCO1B1
	AA Change: p.N130D
	DNA Change: NM_006446.5:c.388A>G
	Chr position (GRCh38): chr12:21176804
	Allelic Frequency: 50%
	Zygosity: Heterozygous
Mutation 2	Gene: SLCO1B1
	AA Change: p.P155T
	DNA Change: NM_006446.5:c.463C>A
	Chr position (GRCh38): chr12:21176879
	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	Figure 1. SLCO1B114 Reference Standard p.N130D Figure 2. SLCO1B114 Reference Standard p.P155T
Storage	2-8°C
Expiry	36 months from the date of manufacture

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