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KCNQ2 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00003785-T01
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-KCNQ2 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 44.3
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-KCNQ2 antibody (H00003785-B01) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00003785-T01
    KCNQ2 transfected lysate.
    Western Blot
    QC Testing of H00003785-T01
    Lane 1: KCNQ2 transfected lysate ( 44.3 KDa)
    Lane 2: Non-transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • Gene Information
  • Entrez GeneID:
  • 3785
  • Protein Accession#:
  • -
  • 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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