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Quantification of Porcine Complement Activation Fragment C3a by a Neoepitope-Based Enzyme-Linked Immunosorbent Assay

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The Complement System

Abstract

Enzyme-linked immunosorbent assay (ELISA) enables fast and simple quantification of analytes in the pico- to nanogram range in complex samples. Here, we describe an ELISA for the detection of porcine C3a as a marker for complement activation. Antibody specificity is critical for a robust assay. This assay is based on a pair of antibodies specific for the porcine C3a molecule and thus does not react with native C3.

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References

  1. Gutierrez K, Dicks N, Glanzner WG, Agellon LB, Bordignon V (2015) Efficacy of the porcine species in biomedical research. Front Genet 6:293

    Article  Google Scholar 

  2. Hopken U, Mohr M, Struber A, Montz H, Burchardi H, Gotze O, Oppermann M (1996) Inhibition of interleukin-6 synthesis in an animal model of septic shock by anti-C5a monoclonal antibodies. Eur J Immunol 26:1103–1109

    Article  CAS  Google Scholar 

  3. Oppermann M, Hopken U, Gotze O (1992) Assessment of complement activation in vivo. Immunopharmacology 24:119–134

    Article  CAS  Google Scholar 

  4. Bergseth G, Ludviksen JK, Kirschfink M, Giclas PC, Nilsson B, Mollnes TE (2013) An international serum standard for application in assays to detect human complement activation products. Mol Immunol 56:232–239

    Article  CAS  Google Scholar 

  5. Mollnes TE, Garred P, Bergseth G (1988) Effect of time, temperature and anticoagulants on in vitro complement activation: consequences for collection and preservation of samples to be examined for complement activation. Clin Exp Immunol 73:484–488

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Skjeflo EW, Sagatun C, Dybwik K, Aam S, Urving SH, Nunn MA, Fure H, Lau C, Brekke OL, Huber-Lang M, Espevik T, Barratt-Due A, Nielsen EW, Mollnes TE (2015) Combined inhibition of complement and CD14 improved outcome in porcine polymicrobial sepsis. Crit Care 19:415

    Article  Google Scholar 

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Correspondence to Per H. Nilsson .

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Nilsson, P.H. et al. (2021). Quantification of Porcine Complement Activation Fragment C3a by a Neoepitope-Based Enzyme-Linked Immunosorbent Assay. In: Roumenina, L.T. (eds) The Complement System. Methods in Molecular Biology, vol 2227. Humana, New York, NY. https://doi.org/10.1007/978-1-0716-1016-9_5

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  • DOI: https://doi.org/10.1007/978-1-0716-1016-9_5

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  • Publisher Name: Humana, New York, NY

  • Print ISBN: 978-1-0716-1015-2

  • Online ISBN: 978-1-0716-1016-9

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