SLCO1B1*15 Reference Standard
CBPA0056
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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 |
| Mutation 1 | AA Change：p.N130D |
| DNA Change：NM_006446.5:c.388A>G | |
| Chr position (GRCh38)：chr12:21176804 A>G | |
| Allelic Frequency：100% | |
| Zygosity：Homozygous | |
| Mutation 2 | AA Change：p.V174A |
| DNA Change：NM_006446.5:c.521T>C | |
| Chr position (GRCh38)：chr12:21178615T>C | |
| Allelic Frequency：100% | |
| Zygosity：Homozygous | |
| 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*15 Reference Standard c.388A>G
Figure 1. SLCO1B1*15 Reference Standard c.521T>C |
| Storage | 4°C |
| Expiry | 36 months from the date of manufacture |
