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<br> The product we spray into the environment should not contain any genetically-modified organisms. So, after we expressed Pantide with <i>E. coli</i>, the LB broth containing <i>E.coli</i> should be first sonicated by the sonicator to let Pantide be soluble in the LB broth. In this step, most of the living <i>E.coli</i> will be eliminated. In order to guarantee the sonicated LB broth lysate is free of <i>E. coli</i>, we boil the lysate for 1 hour. However, boiling the solution may induce Pantide degradation. We want to know the degradation time of boiling the lysate. Pantide are retained and we run SDS-PAGE to evaluate the amount of Pantide residue. (Figure. 1) | <br> The product we spray into the environment should not contain any genetically-modified organisms. So, after we expressed Pantide with <i>E. coli</i>, the LB broth containing <i>E.coli</i> should be first sonicated by the sonicator to let Pantide be soluble in the LB broth. In this step, most of the living <i>E.coli</i> will be eliminated. In order to guarantee the sonicated LB broth lysate is free of <i>E. coli</i>, we boil the lysate for 1 hour. However, boiling the solution may induce Pantide degradation. We want to know the degradation time of boiling the lysate. Pantide are retained and we run SDS-PAGE to evaluate the amount of Pantide residue. (Figure. 1) | ||
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<p class="content-image">Figure1. SDS-PAGE gel and the concentrations of boiling test to native Hv1a-lectin (17.1 kDa). The marked band shows that there is a significant decrease in Hv1a-lectin after 2 hours.</p> | <p class="content-image">Figure1. SDS-PAGE gel and the concentrations of boiling test to native Hv1a-lectin (17.1 kDa). The marked band shows that there is a significant decrease in Hv1a-lectin after 2 hours.</p> | ||
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Latest revision as of 03:08, 4 November 2016