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 |