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

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RQP10620
FormatGenomic DNA
DescriptionAR (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 1DNA Change: c.2632A>G
AA Change: p.T878A
Zygosity: Homozygous
Allelic Frequency: 100%
Cosmic ID: COSM236693
Chr position(GRCh37): chrX:66943552
Mutation 2DNA Change: c.2105T>A
AA Change: p.L702H
Zygosity: Homozygous
Allelic Frequency: 100%
Chr position(GRCh37): chrX:66931463
Cosmic ID: COSM238553
Mutation typeSubstitution - Missense
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencing

Figure 1. AR p.T878A

Figure 2. AR p.L702H

Storage4℃
Expiry36 months from the date of manufacture