MSH2 Deletion Reference Standard
CBPR0003
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索取COA
产品描述
产品数据库
| Introduction | |
| Format | Genomic DNA |
| Description | MSH2 (MutS Homolog 2) is a Protein Coding gene. Diseases associated with MSH2 include Lynch Syndrome 1 and Muir-Torre Syndrome. Among its related pathways are DNA repair pathways, full network and Gene expression (Transcription). |
| Technical Data | |
| Gene | MSH2 |
| DNA Change | N/A |
| AA Change | N/A |
| Zygosity | Homozygous |
| Allelic Frequency | 100% |
| Chr position (GRCh37) | chr2:47636777-47689469 del |
| 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 |  |
| Storage | 2-8°C |
| Expiry | 36 months from the date of manufacture |
