12 research outputs found

    Antigen accessibility to antibodies in different constructs.

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    <p>Intact spores were incubated with mouse anti-M2e primary antibody followed by incubation with goat anti-mouse IgG peroxidase secondary antibodies. 10<sup>4</sup> spores were incubated in TMB substrate solution to develop color reaction. Absorbance was measured at 450 nm and data are given as arithmetic mean with ±SD from three independent experiments.</p

    Efficiency of antigen expression in constructed strains.

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    <p>Data are given as arithmetic mean with ±SD from three independent experiments.</p

    Germinantion of recombinant and parental strain induced by L-alanine and AGFK.

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    <p>Germination was followed by measuring the absorbance decrease at 600 nm of the spore suspension. Data are given as arithmetic mean from three independent experiments.</p

    Western blot analysis of fusion genes expression.

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    <p>Spore coat proteins were extracted and analyzed by western blotting with anti-influenza M2 mAb. Numbers of lanes refer to the strain used in experiment: 1-<i>B</i>. <i>subtilis</i> 168; 2-BTL20(CotC-M2eH-A-S-H, ~20 kDa); 3-BTL21(CotB-M2eH-A-S-H, ~43 kDa); 4-BTL23(CotB-LINKER-M2eH-A-S-H, ~44 kDa); 5-BTL22(CotZ-M2eH-A-S-H, ~28 kDa); 6-BTL24(CotZ-LINKER-M2eH-A-S-H, ~29 kDa); 7-BTL25(CgeA-M2eH-A-S-H, ~26 kDa); 8-BTL26(CgeA-LINKER-M2eH-A-S-H, ~27 kDa).</p

    ELISA of anti-M2e IgG isotyping.

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    <p>IgG1, IgG2a and IgG2b subtypes were tested using mouse sera from 61<sup>st</sup> day of immunization. The titers were expressed as the endpoint dilutions that remained positively detectable. The data are presented as arithmetic mean ±SD of 3 mice per group.</p

    Western blot analysis of sera from immunized mice.

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    <p>5 groups of 3 mice (A, B, C) were orally immunized with recombinant spores of strains <i>B</i>. <i>subtilis</i> 168; 2-BTL20(CotC-M2eH-A-S-H), BTL21(CotB-M2eH-A-S-H), BTL22(CotZ-M2eH-A-S-H) or BTL25(CgeA-M2eH-A-S-H). A 15 μg of recombinant M2eH-A-S-H-GST was separated in polyacrylamide gel and further electrotransferred on nitrocellulose which was further incubated with sera from immunized mice as a primary antibodies. Blots were developed using anti-mouse alkaline phosphatase conjugates. Figure is a merge of 20 different single-lane blot strips.</p
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