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索取COA
产品描述
产品数据库
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 | 4°C |
Expiry | 36 months from the date of manufacture |