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KCNH2 polyclonal antibody

  • Catalog # : PAB27751
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of KCNH2.
  • Immunogen:
  • A synthetic peptide corresponding to 17 amino acid at internal region of human KCNH2.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Monkey, Mouse, Rat
  • Specificity:
  • BLAST analysis of the peptide immunogen showed no homology with other human proteins.
  • Form:
  • Liquid
  • Purification:
  • Immunoaffinity chromatography
  • Recommend Usage:
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (10 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.09% sodium azide)
  • Storage Instruction:
  • Store at 4°C. For long term storage store at -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) of human brain, cerebellum with KCNH2 polyclonal antibody (Cat # PAB27751). Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Gene Information
  • Entrez GeneID:
  • 3757
  • Gene Name:
  • KCNH2
  • Gene Alias:
  • ERG1,HERG,HERG1,Kv11.1,LQT2,SQT1
  • Gene Description:
  • potassium voltage-gated channel, subfamily H (eag-related), member 2
  • Gene Summary:
  • This gene encodes a voltage-activated potassium channel belonging to the eag family. It shares sequence similarity with the Drosophila ether-a-go-go (eag) gene. Mutations in this gene can cause long QT syndrome type 2 (LQT2). Transcript variants encoding distinct isoforms have been identified. [provided by RefSeq
  • Other Designations:
  • cause of Long QT Syndrome Type 2,ether-a-go-go-related potassium channel protein,human eag-related,potassium channel HERG,potassium channel HERG1,potassium voltage-gated channel, subfamily H, member 2,voltage-gated potassium channel,voltage-gated potassiu
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