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KCNQ2 Pre-design Chimera RNAi

  • Catalog # : H00003785-R03
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Homo sapiens potassium voltage-gated channel, KQT-like subfamily, member 2 (KCNQ2), transcript variant 1, mRNA.
  • Reactivity:
  • Human
  • Supplied Product:
  • DEPC water
  • Target Refseq:
  • NM_172107
  • Storage Instruction:
  • Store at -20°C, do not exceed 4 - 5 freeze-thaw cycles to ensure product integrity.
  • Note:
  • Position of the Chimera RNAi.
    The related RNAi products listed below were designed from different accesion number but sharing the same RNAi sequence.

  • Publication Reference
  • Applications
  • RNAi Knockdown
  • Application Image
  • RNAi Knockdown
  • Gene Information
  • Entrez GeneID:
  • 3785
  • Gene Name:
  • KCNQ2
  • Gene Alias:
  • BFNC,EBN,EBN1,ENB1,HNSPC,KCNA11,KV7.2,KVEBN1
  • Gene Description:
  • potassium voltage-gated channel, KQT-like subfamily, member 2
  • Gene Summary:
  • The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • neuroblastoma-specific potassium channel protein,potassium voltage-gated channel KQT-like protein 2
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