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        <identifier>oai:www.ideals.illinois.edu:2142/71336</identifier>
        <datestamp>2023-07-11</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_16405</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:creator>Montealegre, Federico Jose</dc:creator>
          <dc:date>2014-12-16T06:35:45Z</dc:date>
          <dc:date>2014-12-16T06:35:45Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1986</dc:date>
          <dc:date>1986</dc:date>
          <dc:description>A two-site enzyme-immunoassay was developed to detect culture-derived Babesia bovis exoantigens. Bovine anti-B. bovis IgG was used as a capture antibody and as a recognizing antibody. A capture antibody concentration of 10 ug/ml and test samples at protein concentrations of 100 ug/ml gave optimal results with the horseradish peroxidase-conjugated bovine anti-B. bovis IgG. The test was sensitive, specific and reproducible. The highest antigenic activity was demonstrated in 24-hour continuous B. bovis cultures in the microaerophilous stationary phase (MASP) system. The test also proved capable of detecting cross-reactivity with Babesia bigemina. Anion-exchange chromatography with a pH gradient was used as a first-step fractionation of B. bovis exoantigens. Most of the antigenic activity was detected at pH 4. Subsequent re-chromatography of this fraction was conducted using size exclusion high performance liquid chromatography (HPLC). These antigens were detected in the 200 Kd peak. Analysis of the partially purified pH 4 using enzyme-linked immunotransfer blot demonstrated electronegative antigens of relative molecular weights of 57 Kd, 55 Kd and 43 K respectively. The major antigenic bands were confirmed in the partially purified HPLC fraction. A purity analysis of the partially purified fractions showed at least two major contaminant groups (gamma and beta proteins) were present.</dc:description>
          <dc:description>The potential applications of the techniques of detection and isolation are discussed in relation to diagnosis and immunoprophylaxis of bovine babesiosis.</dc:description>
          <dc:description>Made available in DSpace on 2014-12-16T06:35:45Z (GMT). No. of bitstreams: 1
8623373.pdf: 2949780 bytes, checksum: 4f1e1b7cbc0f6b8e288e7b69f45540d1 (MD5)
  Previous issue date: 1986</dc:description>
          <dc:description>Embargo set by: Seth Robbins for item 71502
Lift date: Forever
Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:description>98 p.</dc:description>
          <dc:description>Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1986.</dc:description>
          <dc:identifier>http://hdl.handle.net/2142/71336</dc:identifier>
          <dc:identifier>(UMI)AAI8623373</dc:identifier>
          <dc:subject>Biology, Veterinary Science</dc:subject>
          <dc:title>Babesia Bovis: Detection and Characterization of Culture-Derived Exoantigens (Immunology, Parasitology)</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Veterinary Medical Science</department>
            <discipline>Veterinary Medical Science</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
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