名稱 | PMP22 Amplification Reference Standard |
型號 | CBP40152 |
報價 | |
特點 | PMP22 Amplification Reference Standard |
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電話:4008750250
號碼:
手機:18066071954
地址:南京市棲霞區(qū)緯地路9號
Email: zhangxiangwen@cobioer.com
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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