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索取COA
产品描述
产品数据库
Introduction | |
Format | Genomic DNA |
Description | CYP1A2 (Cytochrome P450 Family 1 Subfamily A Member 2) is a Protein Coding gene. Diseases associated with CYP1A2 include Porphyria Cutanea Tarda and Acetaminophen Metabolism. Among its related pathways are Glucose / Energy Metabolism and Arachidonic acid metabolism. |
Technical Data | |
Mutation 1 | Gene: CYP1A2 |
AA Change: N/A | |
DNA Change: NM_000761.5 c.-3860G>A | |
Chr position (GRCh38): chr15:74745879 G>A | |
Allelic Frequency: 50% | |
Zygosity: Heterozygous | |
Mutation 2 | Gene: CYP1A2 |
AA Change: p.L516L | |
DNA Change: NM_000761.5 c.1548 T>C | |
Chr position (GRCh38): chr15:74755085 T>C | |
Allelic Frequency: 100% | |
Zygosity: Homozygous | |
Mutation 3 | Gene: CYP1A2 |
AA Change: N/A | |
DNA Change: NM_000761.5 c.-163C>A | |
Chr position (GRCh38): chr15:74749576 C>A | |
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. CYP1A2*1L Reference Standard NM_000761.5 c.-3860G>A
Figure 2. CYP1A2*1L Reference Standard p.L516L
Figure 3. CYP1A2*1L Reference Standard NM_000761.5 c.-163C>A |
Storage | 2-8°C |
Expiry | 36 months from the date of manufacture |