diff --git a/wiki/menu.html b/wiki/menu.html index 9957270c5682fa4865f49bb17cf238e08ed24a8a..510cf74c77883cc0a43fc1d042b3038c859b500d 100644 --- a/wiki/menu.html +++ b/wiki/menu.html @@ -73,12 +73,6 @@ </a> <span class="underline"></span> </li> - <li> - <a class="dropdown-item" href="{{ url_for('pages', page='education_communication') }}"> - Education & Communication - </a> - <span class="underline"></span> - </li> <li> <a class="dropdown-item" href="{{ url_for('pages', page='collaborations') }}">Collaborations</a> <span class="underline"></span> @@ -91,9 +85,23 @@ <!---- EDUCATION ----> <li class="nav-item dropdown"> - <a class="nav-link dropdown" href="{{ url_for('pages', page='education') }}" role="button"> + <a class="nav-link dropdown" href="#" id="navbarDropdown12" role="button" data-bs-toggle="dropdown" + aria-expanded="false"> <span>EDUCATION</span> </a> + <ul class="dropdown-menu" aria-labelledby="navbarDropdown12"> + <li> + <a class="dropdown-item" href="{{ url_for('pages', page='education') }}"> + Education + </a> + <span class="underline"></span> + </li> + <li> + <a class="dropdown-item" href="{{ url_for('pages', page='education_communication') }}"> + Education & Communication + </a> + </li> + </ul> </li> <!---- INCLUSIVITY ----> diff --git a/wiki/pages/contribution.html b/wiki/pages/contribution.html index 5190f8904e7410cff6f4c854198dd7b033d3209e..0b01d25c33066c24f6a635a10df97b11d56c7b52 100644 --- a/wiki/pages/contribution.html +++ b/wiki/pages/contribution.html @@ -60,16 +60,16 @@ Driven by the central importance of promoters in regulating gene expression, this year, we continue the characterization of yeast promoters. After careful examination of the iGEM part registry, we chose two constitutive promoters - <i>pREV1</i> and <i>pPAB1</i>, and one inducible promoter <i>pFUS1</i> (Table 1). Constitutive <i>pREV1<i> and - <i>pPAB1</i> promoters were characterized using Venus fluorescent protein as a reporter, while EGFP was used - in the - experiments with the inducible <i>pFUS1</i>. Integration vectors carrying the coding sequences of these - fluorescent - proteins under the control of target promoters were transformed into yeast cells. The resultant yeast - strains were - analyzed by quantitative fluorescence microscopy, and the fluorescence intensity of the reporter protein was - used as - a measure of promoter activity. + <i>pREV1</i> and <i>pPAB1</i>, and one inducible promoter <i>pFUS1</i> (Table 1). Constitutive <i>pREV1</i> and + <i>pPAB1</i> promoters were characterized using Venus fluorescent protein as a reporter, while EGFP was used + in the + experiments with the inducible <i>pFUS1</i>. Integration vectors carrying the coding sequences of these + fluorescent + proteins under the control of target promoters were transformed into yeast cells. The resultant yeast + strains were + analyzed by quantitative fluorescence microscopy, and the fluorescence intensity of the reporter protein was + used as + a measure of promoter activity. </p> <div class="table-wrapper fade_from_right width-8"> <p class="table-desc">