FGF20 (NM_019851) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC214423L1V
- LentiORF®
Lenti ORF particles, FGF20 (Myc-DDK tagged) - Human fibroblast growth factor 20 (FGF20), 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
Product Data | |
Product Name | FGF20 (NM_019851) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | FGF-20; RHDA2 |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_019851 |
ORF Size | 633 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC214423).
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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_019851.1, NP_062825.1 |
RefSeq Size | 1016 bp |
RefSeq ORF | 636 bp |
Locus ID | 26281 |
Protein Families | Secreted Protein |
Protein Pathways | MAPK signaling pathway, Melanoma, Pathways in cancer, Regulation of actin cytoskeleton |
MW | 23.3 kDa |
Gene Summary | The protein encoded by this gene is a member of the fibroblast growth factor family. The fibroblast growth factors 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 product is a secreted neurotrophic factor but lacks a typical signal peptide. It is expressed in normal brain, particularly the cerebellum, and may regulate central nervous system development and function. Homodimerization of this protein was shown to regulate its receptor binding activity and concentration gradient in the extracellular matrix. Genetic variations of this gene have been associated with Parkinson disease susceptibility. [provided by RefSeq, Oct 2009] |
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