ChrMT_ m.1555 A>G Reference Standard
CBPD0031
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索取COA
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| Introduction | |
| Format | Genomic DNA |
| Description | 线粒体基因突变是导致遗传性耳聋的一个重要原因，位于线粒体基因上的A1555G突变、C1494T突变与氨基糖苷类药物性耳聋的发生密切相关。 |
| Technical Data | |
| DNA Change | m.1555 A>G |
| AA Change | N/A |
| Zygosity | Homozygous |
| Allelic Frequency | 100% |
| Chr position (GRCh38) | N/A |
| Transcript | NC_012920.1 |
| 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 | Download for COA |
| Storage | 2-8°C |
| Expiry | 36 months from the date of manufacture |
