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    <p>Hi all,</p>
    <p>fully agree with Ana G!</p>
    <p>Bruno</p>
    <p><br>
    </p>
    <p>+++</p>
    <p><br>
    </p>
    <div class="moz-cite-prefix">On 12/2/2020 20:08, Ana Gisele da Costa
      Neves Ferreira wrote:<br>
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cite="mid:CAPgscZgPbMt4iH0pEp78ubr9GcpBron65EWcFpY2r6xwcwSUcg@mail.gmail.com">
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        <div dir="ltr">Dear Borries,
          <div>As Amy suggested before, I think the first ideia would be
            to use the same experimental conditions assayed by
            Matsui (attached paper). For SV-AUC experiments, the toxin
            was dissolved in 20 mM Tris-HCl pH 8.0 and 200 mM NaCl at a
            concentration of 1 mg/mL in the presence or absence of 1%
            (w/v) SDS. SDS titration seems to be a good idea too. </div>
          <div>Regarding NMR, what kind of experiment are you planning ?</div>
          <div>Regards,</div>
          <div>AnaG</div>
        </div>
        <br>
        <div class="gmail_quote">
          <div dir="ltr" class="gmail_attr">Em qua., 12 de fev. de 2020
            às 18:02, Borries Demeler <<a
              href="mailto:demeler@gmail.com" target="_blank"
              moz-do-not-send="true">demeler@gmail.com</a>> escreveu:<br>
          </div>
          <blockquote class="gmail_quote" style="margin:0px 0px 0px
            0.8ex;border-left:1px solid
            rgb(204,204,204);padding-left:1ex">Dear Ana and Bruno,<br>
            We are gearing up to start the AUC experiment in the
            presence of SDS.<br>
            Bruno, could you please go into your LIMS account at:<br>
            <br>
                    <a
              href="https://uslims.uleth.ca/uslims3_CCH/login.php"
              rel="noreferrer" target="_blank" moz-do-not-send="true">https://uslims.uleth.ca/uslims3_CCH/login.php</a><br>
            <br>
            and update your LIMS project ("Myotoxin-II at high
            concentration") and <br>
            explain in the "Buffer Components" and "Experimental Design"
            section <br>
            how we should prepare the buffer and protein, i.e., what SDS<br>
            concentrations to use, what buffer to use, what protein
            concentrations<br>
            to try. My suggestion would be to use a moderate
            concentration (say, 0.5<br>
            OD 280 nm), and perhaps do a SDS titration, but want to
            defer to you<br>
            or Ana in case you have a better idea.<br>
            <br>
            Amy is planning the experiments for the end of this week and
            it would be <br>
            good to get this info soon.<br>
            <br>
            On another topics:<br>
            Paul and TOny: We have sufficient new material on hand to
            run the<br>
            baseline NMR experiments on Myotoxin now. Please send Amy
            instructions<br>
            for what concentration, buffer etc. you will need and we
            will bring it<br>
            to you. WHen can we run the NMR experiments?<br>
            <br>
            Thanks, -Borries<br>
            _______________________________________________<br>
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                    <div><span
style="color:rgb(11,83,148);font-family:tahoma,sans-serif;font-size:x-small">Ana
                        Gisele da C. Neves Ferreira</span><br>
                    </div>
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      <pre class="moz-quote-pre" wrap="">_______________________________________________
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    </blockquote>
    <pre class="moz-signature" cols="72">-- 
Bruno Lomonte, Ph.D.
Instituto Clodomiro Picado
Universidad de Costa Rica
San José, 11501
COSTA RICA

<a class="moz-txt-link-abbreviated" href="mailto:bruno.lomonte@ucr.ac.cr">bruno.lomonte@ucr.ac.cr</a>
tel. +506  2511 7888
cel. +506  8392 0012

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