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SLCO1B1*1 Reference Standard

CBPA0116

詢 價
索取COA
產(chǎn)品描述
產(chǎn)品數(shù)據(jù)庫
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*15 WT
AA Change: p.N130D
DNA Change: NM_006446.5:c.388A>G
Chr position (GRCh38): chr12:21176804
Allelic Frequency: 0%
Zygosity: Wlid Type
Mutation 2 Gene: SLCO1B1*5/15 WT
AA Change: p.V174A
DNA Change:  NM_006446.5:c.521T>C
Chr position (GRCh38): chr12:21178615
Allelic Frequency: 0%
Zygosity: Wlid Type
Mutation 3 Gene: SLCO1B1*14 WT
AA Change: p.P155T
DNA Change:  NM_006446.5:c.463C>A
Chr position (GRCh38): chr12:21176879
Allelic Frequency: 0%
Zygosity: Wlid Type
   
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. SLCO1B1*1 Reference Standard p.N130D

Figure 2. SLCO1B1*1 Reference Standard p.V174A

Figure 3. SLCO1B1*1 Reference Standard p.P155T

Storage 2-8°C
Expiry 36 months from the date of manufacture

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