SLCO1B1*1 Reference Standard

CBPA0075

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
Gene	SLCO1B1
SLCO1B1*5 WT	AA Change: p.V174A
	DNA Change: NM_006446.5:c.521T>C
	Chr position (GRCh38): NC_000012.11:g.21331549T>C
	Zygosity: Wlid Type
	Allelic Frequency: 0%
SLCO1B1*15 WT	AA Change: p.N130D
	DNA Change: NM_006446.5:c.388A>G
	Chr position (GRCh38): NC_000012.11:g.21329738A>G
	Zygosity: Wlid Type
	Allelic Frequency: 0%

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. Sanger of SLCO1B15 WT Figure 2. Sanger of SLCO1B115 WT
Storage	2-8°C
Expiry	36 months from the date of manufacture

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