AI-Edigene? EGFR p.G719A Reference Standard Plus
CBP10414
詢 價
索取COA
產品描述
產品數(shù)據(jù)庫
| Introduction | |
| Format | Genomic DNA |
| Description | The G719A mutation results in an amino acid substitution at position 719 in EGFR, from a glycine (G) to an alanine (A). This mutation occurs within exon 18, which encodes part of the kinase domain. |
| Technical Data | |
| DNA Change | c.2156G>C |
| AA Change | p.G719A |
| Mutation type | Substitution - Missense |
| Zygosity | Homozygous |
| Allelic Frequency | 100% |
| Transcript | ENST00000275493 |
| Cosmic ID | COSM6239 |
| Chr position(GRCh37) | chr7:55241708 |
| 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 | 4℃ |
| Expiry | 36 months from the date of manufacture |
