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基因檢測(cè)標(biāo)準(zhǔn)品 > Mutation > CBP10620AR p.T878A/p.L702H double mutation Reference Stand

AR p.T878A/p.L702H double mutation Reference Stand
名稱(chēng) AR p.T878A/p.L702H double mutation Reference Stand
型號(hào) CBP10620
報(bào)價(jià)
特點(diǎn) AR p.T878A/p.L702H double mutation Reference Standard
  • 詳細(xì)內(nèi)容
 CBP10620
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

CBP10620 p.T878A sanger 1.jpg

Figure 1. AR p.T878A

CBP10620 p.L702H sanger2.jpg

Figure 2. AR p.L702H

Storage4℃
Expiry36 months from the date of manufacture

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