Identify and characterize EBV-specific antibody responses on the epitope level
Download the PEPperCHIP® Epstein-Barr Virus Peptide Microarray data sheet

A study by Bjornevik et al. (Science, 2022) recently reported evidence of a causal link between previous EBV infection and the development of multiple sclerosis (MS), a demyelinating disease of the central nervous system. Viruses have previously been suggested as potential causative agents in several other autoimmune diseases, warranting a closer look at the immunology of antiviral responses.

The new PEPperCHIP® Epstein-Barr Virus Peptide Microarray contains the most immunogenic EBV antigens from the Immune Epitope Database converted into over 5,500 individual peptides. The microarray enables you to:

  • Screen patient sera for EBV-specific antibody responses with amino acid resolution
  • Investigate anti-EBV antibody fingerprints of MS patients vs. healthy controls
  • Investigate autoantibody responses before and after COVID-19 vaccination
  • Correlate IgG or IgA autoantibodies with disease progression
  • Identify and characterize epitopes for EBV biomarker discovery, IVD, or vaccine development
Learn more

Interested in analyzing your own selection of antigens? Get in touch with one of our scientists to find out how to get your own custom microarray.
Research consortium starts GENImmune project for new methods
to design vaccines for efficient SARS-CoV-2 immunization
New research consortium for vaccine design
PEPperPRINT joins Biomax Informatics and PMCR, together with academic research partners in a new project aiming to employ AI-based approaches for vaccine design.

Read the joint press release
Partner with us at BIO-Europe Spring 2022
Partner with us at BIO-Europe Spring
Partnering is now open for this year's BIO-Europe digital event. Connect with us through the PartneringONE platform until March 21 to schedule a meeting.

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Epitope-Specific Anti-C1q Autoantibodies in Systemic Lupus Erythematosus
Autoantibody Epitopes in Lupus
Kleer et. al report specific autoantibody epitopes against a complement component that are associated with certain disesase manifestations in Lupus.

Read the paper
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