| 名稱 | PMP22 Amplification Reference Standard |
| 型號(hào) | CBP40152 |
| 報(bào)價(jià) |  |
| 特點(diǎn) | PMP22 Amplification Reference Standard |
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基因檢測標(biāo)準(zhǔn)品 > CNV > CBP40152PMP22 Amplification Reference Standard
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PMP22 Amplification Reference Standard
| Introduction | ||||
| Format | Genomic DNA | |||
| Description | This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. | |||
| Technical Data | ||||
| Copy number | 3 | |||
| Definition | Amplication | |||
| Product Information | ||||
| Intended Use | Research Use Only | |||
| Unit Size | 1ug | |||
| Concentration | Download for COA | |||
| Purity | Download for COA | |||
| DNA electrophoresis | Download for COA | |||
| Sanger sequencing | Download for COA | |||
| Storage | 4℃ | |||
| Expiry | 36 months from the date of manufacture | |||
PMP22 Amplification Reference Standard
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