Anti-KCNQ1 (7E1) Mouse antibody

Cat.#: 168425

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Product Information

  • Product Name
    Anti-KCNQ1 (7E1) Mouse antibody
  • Documents
  • Description
    KCNQ1 (7E1) Mouse monoclonal antibody
  • Tested applications
    WB, FC
  • Species reactivity
    Human
  • Isotype
    Mouse IgG2b
  • Preparation
    Antigen: Purified recombinant fragment of human KCNQ1 expressed in E. Coli.
  • Clonality
    Monoclonal
  • Formulation
    Ascitic fluid containing 0.03% sodium azide.
  • Storage instructions
    Store at 4°C short term. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Applications

    WB: 1/500 - 1/2000

    FC: 1/200 - 1/400

    ELISA: 1/10000

  • Validations

    Western blot detection of KCNQ1 in C6,Jurkat,K562 and 3T3 cell lysates using KCNQ1 mouse mAb (1:3000 diluted).Predicted band size:95KDa.Observed band size:95KDa.

    Western blot detection of KCNQ1 in C6,Jurkat,K562 and 3T3 cell lysates using KCNQ1 mouse mAb (1:3000 diluted).Predicted band size:95KDa.Observed band size:95KDa.

    Western blot analysis using KCNQ1 mouse mAb against MCF-7 (1) and A431 (2) cell lysate.

    Western blot analysis using KCNQ1 mouse mAb against MCF-7 (1) and A431 (2) cell lysate.

    Flow cytometric analysis of MCF-7 cells using KCNQ1 mouse mAb (green) and negative control (red).

    Flow cytometric analysis of MCF-7 cells using KCNQ1 mouse mAb (green) and negative control (red).

  • Background
    Swiss-Prot Acc.P51787.This gene encodes a voltage-gated potassium channel required for repolarization phase of the cardiac action potential. This protein can form heteromultimers with two other potassium channel proteins, KCNE1 and KCNE3. Mutations in this gene are associated with hereditary long QT syndrome 1 (also known as Romano-Ward syndrome), Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation. This gene exhibits tissue-specific imprinting, with preferential expression from the maternal allele in some tissues, and biallelic expression in others. This gene is located in a region of chromosome 11 amongst other imprinted genes that are associated with Beckwith-Wiedemann syndrome (BWS), and itself has been shown to be disrupted by chromosomal rearrangements in patients with BWS. Alternatively spliced transcript variants have been found for this gene.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"