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AR p.T878A/p.L702H double mutation Reference Standard

CBP10620

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索取COA
产品描述
产品数据库
Introduction 
Format Genomic DNA
Description AR (Androgen Receptor) is a Protein Coding gene. Diseases associated with AR include Androgen Insensitivity, Partial and Spinal And Bulbar Muscular Atrophy, X-Linked 1.
   
Technical Data 
Mutation 1 DNA Change: c.2632A>G
AA Change: p.T878A
Zygosity: Homozygous
Allelic Frequency: 100%
Cosmic ID: COSM236693
Chr position(GRCh37): chrX:66943552
Mutation 2 DNA Change: c.2105T>A
AA Change: p.L702H
Zygosity: Homozygous
Allelic Frequency: 100%
Chr position(GRCh37): chrX:66931463
Cosmic ID: COSM238553
Mutation type Substitution - Missense
Buffer Tris-EDTA
   
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. AR p.T878A

Figure 2. AR p.L702H

Storage 2-8℃
Expiry 36 months from the date of manufacture

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