| RQPA0075 | |
| 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 SLCO1B1*5 WT
Figure 2. Sanger of SLCO1B1*15 WT |
| Storage | 4°C |
| Expiry | 36 months from the date of manufacture |
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