Eif4e (BC010759) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR202403L3V
- LentiORF®
Lenti ORF particles, Eif4e (Myc-DDK-tagged) - Mouse eukaryotic translation initiation factor 4E (cDNA clone MGC:18497 IMAGE:4216609), 200ul, >10^7 TU/mL
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CNY 6,650.00
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Specifications
Product Data | |
Product Name | Eif4e (BC010759) Mouse Tagged ORF Clone Lentiviral Particle |
Synonyms | Eif4e-ps, eIF-4E |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | BC010759 |
ORF Size | 651 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR202403).
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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 | BC010759.1 |
RefSeq Size | 1646 bp |
RefSeq ORF | 653 bp |
Locus ID | 13684 |
Gene Summary | This gene encodes a component of the eukaryotic translation initiation factor 4F complex, which recognizes the 7-methylguanosine cap structure at the 5' end of messenger RNAs. The encoded protein aids in translation initiation by recruiting ribosomes to the 5'-cap structure. Association of this protein with the 4F complex is the rate-limiting step in translation initiation. This gene acts as a proto-oncogene, and its expression and activation is associated with transformation and tumorigenesis. It has also been associated with autism spectrum disorders. Consistently, knockout of this gene results in increased translation of neuroligins, postsynaptic proteins linked to autism spectrum disorders. Pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
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