SLCO1B1*5/*15 Reference Standard

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RQPA0077 
FormatGenomic DNA
DescriptionSLCO1B1 (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 
GeneSLCO1B1
SLCO1B1*5AA Change:p.V174A
DNA Change:NM_006446.5:c.521T>C
Chr position (GRCh38):NC_000012.11:g.21331549T>C
Allelic Frequency:50%
Zygosity:Heterozygous
SLCO1B1*15AA Change:p.N130D
DNA Change:NM_006446.5:c.388A>G
Chr position (GRCh38):NC_000012.11:g.21329738A>G
Allelic Frequency:50%
Zygosity:Heterozygous
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencingDownload for COA
Storage4°C
Expiry36 months from the date of manufacture