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 | 4℃ |
| Expiry | 36 months from the date of manufacture |
