United States
Germany
Japan
United Kingdom
China
PMP22 (NM_153322) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC218781L4V
- LentiORF®
-
Lenti ORF particles, PMP22 (mGFP-tagged) - Human peripheral myelin protein 22 (PMP22), transcript variant 3, 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 8,360.00
Product images
CNY 1,999.00
CNY 2,700.00
Specifications
| Product Data | |
| Product Name | PMP22 (NM_153322) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CIDP; CMT1A; CMT1E; DSS; GAS-3; GAS3; HMSNIA; HNPP; Sp110 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_153322 |
| ORF Size | 480 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC218781).
|
| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_153322.1 |
| RefSeq Size | 1669 bp |
| RefSeq ORF | 483 bp |
| Locus ID | 5376 |
| Protein Families | Transmembrane |
| MW | 17.7 kDa |
| Gene Summary | 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. [provided by RefSeq, Jul 2013] |
Documents
| Product Manuals |
| FAQs |
| SDS |
