| RQPA0077 | |
| 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. |
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| Technical Data |
| Gene | SLCO1B1 |
| SLCO1B1*5 | AA Change:p.V174A |
| DNA Change:NM_006446.5:c.521T>C |
| Chr position (GRCh38):NC_000012.11:g.21331549T>C |
| Allelic Frequency:50% |
| Zygosity:Heterozygous |
| SLCO1B1*15 | AA Change:p.N130D |
| DNA Change:NM_006446.5:c.388A>G |
| Chr position (GRCh38):NC_000012.11:g.21329738A>G |
| Allelic Frequency:50% |
| Zygosity:Heterozygous |
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| 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 | Download for COA |
| Storage | 4°C |
| Expiry | 36 months from the date of manufacture |