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SR317027

KSR2 Human siRNA Oligo Duplex (Locus ID 283455)

Origene Technologies, Inc.

DESCRIPTION

KSR2 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each

DETAILS

  • Note: Single siRNA duplex (10nmol) can be ordered.
  • Purity: HPLC purified
  • Refseq: NM_173598
  • Status: In Stock*
  • Summary: Location-regulated scaffold connecting MEK to RAF. Has very low protein kinase activity and can phosphorylate MAP2K1 at several Ser and Thr residues with very low efficiency (in vitro). Interaction with BRAF enhances KSR2-mediated phosphorylation of MAP2K1 (in vitro). Blocks MAP3K8 kinase activity and MAP3K8-mediated signaling. Acts as a negative regulator of MAP3K3-mediated activation of ERK, JNK and NF-kappa-B pathways, inhibiting MAP3K3-mediated interleukin-8 production.[UniProtKB/Swiss-Prot Function]
  • Category: RNAi
  • Sequences: Available with shipment
  • Stability: One year from date of shipment when stored at -20°C.
  • Components: KSR2 (Human) - 3 unique 27mer siRNA duplexes - 2 nmol each (Locus ID 283455)Included - SR30004, Trilencer-27 Universal Scrambled Negative Control siRNA Duplex - 2 nmolIncluded - SR30005, RNAse free siRNA Duplex Resuspension Buffer - 2 ml Need an individual siRNA?
  • Uniprot Id: Q6VAB6
  • Availability: In Stock
  • Quality Control: Tested by ESI-MS
  • 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).
  • Number of Transfections: Approximately 330 transfections/2nmol in 24-well plate under optimized conditions (final conc. 10 nM).