United States
Germany
Japan
United Kingdom
China
MMP20 (NM_004771) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC220786L4V
- LentiORF®
-
Lenti ORF particles, MMP20 (mGFP-tagged) - Human matrix metallopeptidase 20 (MMP20), 200ul, >10^7 TU/mL
Need custom lentivirus service?
Get a free quote
CNY 10,450.00
货期*
详询
规格
Product images
经常一起买 (3)
Specifications
| Product Data | |
| Product Name | MMP20 (NM_004771) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | AI2A2; MMP-20 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_004771 |
| ORF Size | 1449 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC220786).
|
| 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_004771.3 |
| RefSeq Size | 1956 bp |
| RefSeq ORF | 1452 bp |
| Locus ID | 9313 |
| Protein Families | Druggable Genome, Secreted Protein, Transmembrane |
| MW | 54.39 kDa |
| Gene Summary | Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The protein encoded by this gene degrades amelogenin, the major protein component of dental enamel matrix, and thus thought to play a role in tooth enamel formation. A mutation in this gene, which alters the normal splice pattern and results in premature termination of the encoded protein, has been associated with amelogenesis imperfecta. This gene is part of a cluster of MMP genes located on chromosome 11q22.3. [provided by RefSeq, Aug 2011] |
Documents
| Product Manuals |
| FAQs |
| SDS |
Resources
You may also need
Customer
Reviews
Loading...
