Hif1a Mouse siRNA Oligo Duplex (Locus ID 15251)

Référence SR420554

Conditionnement : 1kit

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Hif1a Mouse siRNA Oligo Duplex (Locus ID 15251)

SKU
SR420554
Hif1a (Mouse) - 3 unique 27mer siRNA duplexes - 2 nmol each
Stability One year from date of shipment when stored at -20°C. # 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_010431 UniProt ID Q61221 Synonyms AA959795; bHLHe7; bHLHe78; HIF-1; HIF-1-alpha; HIF1; HIF1-alpha; HIF1alpha; MO; MOP1 Summary This gene encodes the alpha subunit which, along with the beta subunit, forms a heterodimeric transcription factor that regulates the cellular and developmental response to reduced oxygen tension. The transcription factor has been shown to regulate genes involved in several biological processes, including erythropoiesis and angiogenesis which aid in increased delivery of oxygen to hypoxic regions. The transcription factor also plays a role in the induction of genes involved in cell proliferation and survival, energy metabolism, apoptosis, and glucose and iron metabolism. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015] 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 tech@clinisciences.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).