• Nature
  • Source
  • Amino Acid Sequence 1
    • Accession
    • Species
    • Additional sequence information
      Observed band of ~185kDa on SDS-PAGE
    Amino Acid Sequence 2
    • Accession
    • Species


Our Abpromise guarantee covers the use of ab65866 in the following tested applications.

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

  • Applications


    IHC - Wholemount

    Western blot



  • Endotoxin level
    < 25.000 Eu/mg
  • Purity
    > 90 % SDS-PAGE.
    Human IgE full length protein was purified by Protein L chromatography. As the IgE comes from a monoclonal cell line, there is no contamination of antibodies of other isotypes. The remaining contaminants are mainly components from Foetal Bovine Serum.
  • Form
  • Additional notes

    This product is purified Human IgE with kappa light chains produced in vitro from a monoclonal hybridoma.

    This antigen is quite unique, because it is the only available IgE product, which originates from a human monoclonal cell line. Our IgE product shows superior advantage when compared to the traditionally purified polyclonal IgE from myeloma patients. A comparison which is highly superior on the following key parameters:.

    - Less batch-to-batch variation

    - Higher degree of purity (>90%)

    - A more uniform product (monoclonal and not polyclonal)


    IgE has been used in a variety of cell stimulation assays, including the following cell types:

    - Human airway smooth muscle (HASM) cells

    - mast cells (MC)

    - Human bronchial/tracheal smooth muscle (B/TSM) cells

    - acute myelogenous leukemia (AML) blasts

    - Human neutrophils

    Low endotoxin levels below < 25 EU/mg allow use of IgE protein in cellular immunology and in cell proliferation studies.

    1 mg of ab65866 is 380,000± 50,000 IU/ml.

  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    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.

    pH: 7.40
    Constituents: 0.00017% PBS, 0.00087% Sodium chloride

    This product is an active protein and may elicit a biological response in vivo, handle with caution.

General Info

  • Alternative names
    • Igh2
    • IGHE
    • IGHEP1
    • Immunoglobulin heavy constant epsilon
  • Relevance
    IgE is the class of antibodies produced in the lungs, skin, and mucous membranes. It may protect against parasite invasion, but it is a major factor in allergic reactions. The antigen-specific IgE interacts with mast cells and eosinophils, triggers the release of histamine, leukotrienes and other substances that lead to the itching, sneezing and congestion of allergies - and the life threatening respiratory distress of asthma and anaphylactic shock.
  • Cellular localization
    Cell Membrane


  • Background-subtracted data values (mean +/- SD) are graphed.

  • SDS-PAGE analysis of:

    Lane 1: Molecular weight markers.
    Lane 2: ab65866.
    Lane 3: IgE purified from serum from a myeloma patient.


This product has been referenced in:
  • Vidal M  et al. Development of quantitative suspension array assays for six immunoglobulin isotypes and subclasses to multiple Plasmodium falciparum antigens. J Immunol Methods N/A:N/A (2018). Read more (PubMed: 29397157) »
  • Wan Z  et al. Photocleavage-based affinity purification of biomarkers from serum: Application to multiplex allergy testing. PLoS One 13:e0191987 (2018). Read more (PubMed: 29389948) »
See all 7 Publications for this product

Customer reviews and Q&As

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1-2 of 2 Abreviews

Competitive ELISA
We developed a quantitative and sensitive immunoassay to determine Human IgE in human serum using gold nanoclusters (AuNCs) as fluorescent labels. The synthesized AuNCs have a particle size of 2.7 ± 0.1 nm, a maximum fluorescence emission at 710 nm and high stability. The covalent bioconjugation of these AuNCs with the antibody was carried out by the carbodiimide reaction. A molar ratio 1:3 (antibody:AuNCs) was selected.

Human IgE from Abcam (ab65866) was used as standard to prepare the calibration curve in PBS and in human serum matrix (attached figure). Two immunoassay configurations were assayed (competitive and sandwich format), obtaining better detection limit with the competitive format (0.2 ng/mL). For both formats the detection limits were better than those obtained with current commercial ELISA kits (12 ng/mL).

Moreover, the developed fluorescent competitive immunoassay offers other interesting advantages such as fewer reagents and simpler procedures.

The applicability of this new AuNCs immunoprobe was successfully demonstrated for the determination of IgE in human serum, using the competitive configuration.

This research has been published in Biosensors and Bioelectronics,


Authors: María Cruz Alonso, Laura Trapiella-Alfonso, José M Costa Fernández, Rosario Pereiro, Alfredo Sanz-Medel

Title: “Functionalized gold nanoclusters as fluorescent labels for immunoassays: Application to Human serum immunoglobulin E determination”

María Cruz

Verified customer

Submitted Sep 29 2015

The hIgE works in my assay. But the labelled concentration is different from the concentration measured by BCA method. I recommend that measuring the concenration before using it.

Abcam user community

Verified customer

Submitted Sep 03 2014

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