United States
Germany
Japan
United Kingdom
China
FGF13 (NM_001139500) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC227498L4V
- LentiORF®
-
Lenti ORF particles, FGF13 (mGFP-tagged)-Human fibroblast growth factor 13 (FGF13), transcript variant 2, 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 | FGF13 (NM_001139500) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | DEE90; FGF-13; FGF2; FHF-2; FHF2; LINC00889 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001139500 |
| ORF Size | 765 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC227498).
|
| 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_001139500.1 |
| RefSeq ORF | 768 bp |
| Locus ID | 2258 |
| Protein Families | Secreted Protein |
| Protein Pathways | MAPK signaling pathway, Melanoma, Pathways in cancer, Regulation of actin cytoskeleton |
| MW | 28.6 kDa |
| Gene Summary | The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008] |
Documents
| Product Manuals |
| FAQs |
| SDS |
