SLCO1B1*14 Reference Standard
CBPA0123
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索取COA
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| 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 |
| AA Change: p.N130D | |
| DNA Change: NM_006446.5:c.388A>G | |
| Chr position (GRCh38): chr12:21176804 | |
| Allelic Frequency: 50% | |
| Zygosity: Heterozygous | |
| Mutation 2 | Gene: SLCO1B1 |
| AA Change: p.P155T | |
| DNA Change: NM_006446.5:c.463C>A | |
| Chr position (GRCh38): chr12:21176879 | |
| Allelic Frequency: 50% | |
| Zygosity: Heterozygous | |
| 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*14 Reference Standard p.N130D
Figure 2. SLCO1B1*14 Reference Standard p.P155T |
| Storage | 2-8°C |
| Expiry | 36 months from the date of manufacture |
