MLH1 Deletion Reference Standard
CBPR0001
询 价
索取COA
产品描述
产品数据库
| Introduction | |
| Format | Genomic DNA |
| Description | MLH1 (MutL Homolog 1) is a Protein Coding gene. Diseases associated with MLH1 include Mismatch Repair Cancer Syndrome 1 and Lynch Syndrome 2. Among its related pathways are DNA repair pathways, full network and Gene expression (Transcription). |
| Technical Data | |
| Gene | MLH1 |
| DNA Change | N/A |
| AA Change | N/A |
| Zygosity | Heterozygous |
| Allelic Frequency | 50% |
| Chr position (GRCh37) | chr3:37051418-37078384 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 |
