CYP2B6*1 Reference Standard
CBPA0126
詢 價
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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 | |
| Mutation 1 | Gene: CYP2B6*15 WT |
| AA Change: p.I391N | |
| DNA Change: NM_000767.5 c. 1171T>A | |
| Chr position (GRCh38): chr19:41012693T>A | |
| Allelic Frequency: 0% | |
| Zygosity: Wlid Type | |
| Mutation 2 | Gene: CYP2B6*4 WT |
| AA Change: p.K262R | |
| DNA Change: NM_000767.5 c.785A>G | |
| Chr position (GRCh38): chr19:41009358A>G | |
| Allelic Frequency: 0% | |
| Zygosity: Wlid Type | |
| Mutation 3 | Gene: CYP2B6*6WT |
| AA Change: p.Q172H | |
| DNA Change: NM_000767.5 c.516G>T | |
| Chr position (GRCh38): chr19:41006936G>T | |
| Allelic Frequency: 0% | |
| Zygosity: Wlid Type | |
| Mutation 4 | Gene: CYP2B6*6WT |
| AA Change: p.K262R | |
| DNA Change: NM_000767.5 c.785A>G | |
| Chr position (GRCh38): chr19:41009358A>G | |
| Allelic Frequency: 0% | |
| Zygosity: Wlid Type | |
| Mutation 5 | Gene: CYP2B6*2 WT |
| AA Change: p.R22C | |
| DNA Change: NM_000767.5 c.64C>T | |
| Chr position (GRCh38): chr19:40991369C>T | |
| Allelic Frequency: 0% | |
| Zygosity: Wlid Type | |
| 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*1 Reference Standard p.I391N
Figure 2. CYP2B6*1 Reference Standard p.K262R
Figure 3. CYP2B6*1 Reference Standard p.Q172H
Figure 4. CYP2B6*1 Reference Standard p.K262R
Figure 5. CYP2B6*1 Reference Standard p.R22C |
| Storage | 2-8°C |
| Expiry | 36 months from the date of manufacture |
