• Product name

  • Description

    Rabbit polyclonal to H-ERG
  • Host species

  • Tested applications

    Suitable for: WBmore details
  • Species reactivity

    Reacts with: Mouse, Rat, Human
    Predicted to work with: Rabbit, Dog
  • Immunogen

    Synthetic peptide corresponding to Human H-ERG aa 880-900.


    Database link: Q12809


  • Form

  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Storage buffer

    Preservative: 0.1% Sodium azide
    Constituents: 50% Glycerol, 49% PBS
  • Concentration information loading...
  • Purity

    Immunogen affinity purified
  • Purification notes

    ab192500 was affinity-purified from Rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
  • Clonality

  • Isotype

  • Research areas


Our Abpromise guarantee covers the use of ab192500 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB Use at an assay dependent concentration. Predicted molecular weight: 126 kDa.


  • Function

    Pore-forming (alpha) subunit of voltage-gated inwardly rectifying potassium channel. Channel properties are modulated by cAMP and subunit assembly. Mediates the rapidly activating component of the delayed rectifying potassium current in heart (IKr). Isoform 3 has no channel activity by itself, but modulates channel characteristics when associated with isoform 1.
  • Tissue specificity

    Highly expressed in heart and brain.
  • Involvement in disease

    Defects in KCNH2 are the cause of long QT syndrome type 2 (LQT2) [MIM:613688]. Long QT syndromes are heart disorders characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. They cause syncope and sudden death in response to exercise or emotional stress. Deafness is often associated with LQT2.
    Defects in KCNH2 are the cause of short QT syndrome type 1 (SQT1) [MIM:609620]. Short QT syndromes are heart disorders characterized by idiopathic persistently and uniformly short QT interval on ECG in the absence of structural heart disease in affected individuals. They cause syncope and sudden death.
  • Sequence similarities

    Belongs to the potassium channel family. H (Eag) (TC 1.A.1.20) subfamily. Kv11.1/KCNH2 sub-subfamily.
    Contains 1 cyclic nucleotide-binding domain.
    Contains 1 PAC (PAS-associated C-terminal) domain.
    Contains 1 PAS (PER-ARNT-SIM) domain.
  • Domain

    The segment S4 is probably the voltage-sensor and is characterized by a series of positively charged amino acids at every third position.
  • Post-translational

    Phosphorylated on serine and threonine residues. Phosphorylation by PKA inhibits ion conduction.
  • Cellular localization

  • Information by UniProt
  • Database links

  • Alternative names

    • eag homolog antibody
    • Eag-related protein 1 antibody
    • ERG antibody
    • ERG-1 antibody
    • ERG1 antibody
    • Ether a go go related potassium channel protein antibody
    • Ether-a-go-go-related gene potassium channel 1 antibody
    • Ether-a-go-go-related protein 1 antibody
    • H ERG antibody
    • H-ERG antibody
    • HERG 1 antibody
    • HERG antibody
    • hERG-1 antibody
    • hERG1 antibody
    • KCNH2 antibody
    • KCNH2_HUMAN antibody
    • Kv11.1 antibody
    • LQT 2 antibody
    • LQT2 antibody
    • Potassium channel HERG antibody
    • Potassium voltage gated channel subfamily H (eag related) member 2 antibody
    • Potassium voltage-gated channel subfamily H member 2 antibody
    • SQT1 antibody
    • Voltage gated potassium channel, subfamily H, member 2 antibody
    • Voltage-gated potassium channel subunit Kv11.1 antibody
    see all


ab192500 has not yet been referenced specifically in any publications.

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