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CYP1A2*1L Reference Standard

CBPA0124

詢 價
索取COA
產品描述
產品數據庫
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

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