Eif4g2 Mouse siRNA Oligo Duplex (Locus ID 13690)

SKU
SR421103
Eif4g2 (Mouse) - 3 unique 27mer siRNA duplexes - 2 nmol each
  $518.00
In Stock*
Specifications
Specifications
Product Data
Purity HPLC purified
Quality Control Tested by ESI-MS
Sequences Available with shipment
Components
Eif4g2 (Mouse) - 3 unique 27mer siRNA duplexes - 2 nmol each (Locus ID 13690)
Included - SR30004, Trilencer-27 Universal Scrambled Negative Control siRNA Duplex - 2 nmol
Included - SR30005, RNAse free siRNA Duplex Resuspension Buffer - 2 ml
Stability One year from date of shipment when stored at -20°C.
Shipping Ambient
# of Transfections Approximately 330 transfections/2nmol in 24-well plate under optimized conditions (final conc. 10 nM).
Note Single siRNA duplex (10nmol) can be ordered.
Reference Data
RefSeq NM_001040131, NM_013507
UniProt ID Q62448
Synonyms DAP; DAP-5; E130105L11Rik; Na; Nat; Nat1; Natm1; p97
Summary Translation initiation is mediated by specific recognition of the cap structure by eukaryotic translation initiation factor 4F (eIF4F), which is a cap binding protein complex that consists of three subunits: eIF4A, eIF4E and eIF4G. The protein encoded by this gene shares similarity with the C-terminal region of eIF4G, that contains the binding sites for eIF4A and eIF3; eIF4G in addition, contains a binding site for eIF4E at the N-terminus. Unlike eIF4G which supports cap-dependent and independent translation, this gene product functions as a general repressor of translation by forming translationally inactive complexes. Transgene expression of the apolipoprotein B mRNA-editing enzyme (APOBEC-1) causes extensive editing of this mRNA, which could contribute to the potent oncogenesis induced by overexpression of APOBEC-1. In vitro and in vivo studies in human indicate that translation of this mRNA initiates exclusively at a non-AUG (GUG) codon. This also appears to be true for mouse. Two alternatively spliced transcript variants that encode different isoforms have been found for this gene. provided by RefSeq, Jul 2008
Performance Guaranteed OriGene guarantees that at least two of the three Dicer-Substrate duplexes in the kit will provide at least 70% or more knockdown of the target mRNA when used at 10 nM concentration by quantitative RT-PCR when the TYE-563 fluorescent transfection control duplex (cat# SR30002) indicates that >90% of the cells have been transfected and the HPRT positive control (cat# SR30003) provides 90% knockdown efficiency.

For non-conforming siRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the siRNA kit. To arrange for a free replacement with newly designed duplexes, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled siRNA control (quantitative RT-PCR data required).
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Documents
Resources

file-alt Citations

The thyroid hormone increases bulk histones expression by enhancing translational efficiency
Zambrano, García-Carpizo, Villamuera et al
Mol. Endocrinol. (2014)
Cited by 2
AI Summary: OriGene contributed to this study by providing siRNA duplexes (SR30004 as control and SR421103A, B, and C targeting mouse Eif4g2) used for gene knockdown experiments to assess the role of EIF4G2 in thyroid hormone-induced histone expression.
Snippet: Small-interfering RNAs (siRNAs) transfections were per- formed by using the TansIT X2 reagent (Myrus) following man- ufacturer's instructions. siRNAs duplexes were purchased from Origene: SR30004 (control), SR421103A, B and C (mouse Eif4g2). ... Cite SaveSaving
Showing 1-1 of 1 papers.
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