CYP2B6*6 Reference Standard
CBPA0037
詢 價
索取COA
產品描述
產品數據庫
| Introduction | |
| Format | Genomic DNA |
| Description | CYP2B6 (Cytochrome P450 Family 2 Subfamily B Member 6) is a Protein Coding gene. Diseases associated with CYP2B6 include Efavirenz, Poor Metabolism Of and Acute Frontal Sinusitis. Among its related pathways are Vortioxetine Pathway, Pharmacokinetics and Oxidation by cytochrome P450. |
| Technical Data | |
| Gene | CYP2B6 |
| Mutation Type 1 | AA Change: p.Q172H |
| DNA Change: NM_000767.5:c.516G>T | |
| Chr position (GRCh38): chr19:41006936G>T | |
| Mutation Type 2 | AA Change: p.K262R |
| DNA Change: NM_000767.5:c.785A>G | |
| Chr position (GRCh38): chr19:41009358A>G | |
| 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. CYP2B6*6 Reference Standard p.Q172H
Figure 2. CYP2B6*6 Reference Standard p.K262R |
| Storage | 2-8°C |
| Expiry | 36 months from the date of manufacture |
