Work w/ Alison

html_app/assignments/mit706s13/gen/instructions.gss.css

@@ -27,3 +27,11 @@
   border: 1px solid #e0e0e0;
   padding-left: 8px;
 }
+.scb_s_mit706s13_assignment_overview {
+  font-family: 'SourceSansPro-Regular';
+  font-size: 12pt;
+  text-align: left;
+}
+.scb_s_mit706s13_assignment_detail {
+  text-align: left;
+}

html_app/assignments/mit706s13/instructions.gss

@@ -34,3 +34,12 @@
     padding-left: 8px;
 }
 
+.scb_s_mit706s13_assignment_overview {
+    font-family: 'SourceSansPro-Regular';
+    font-size:12pt;
+    text-align: left;
+}
+
+.scb_s_mit706s13_assignment_detail {
+    text-align: left;
+}

html_app/assignments/mit706s13/instructions.soy

@@ -6,7 +6,7 @@
 {template .assignment_overview}
 <div class='scb_s_mit706s13_assignment_overview' xmlns="http://www.w3.org/1999/html"
      xmlns="http://www.w3.org/1999/html" xmlns="http://www.w3.org/1999/html">
-    This assignment is due at beginning of lecture (9:30 am) on Thursday, April 25th, 2013
+    This extra credit assignment is due at the beginning of lecture (9:30 am) on Thursday, April 25th, 2013.<br>
     (Up to 5 points)
     <h2>Goal</h2>
     The goal of this assignment is to enhance learning of experimental design and analysis by providing you with the
@@ -58,13 +58,12 @@
         <div>1</div>
     </div>
     <div class='scb_objective_text'>
-        <p>
+
         To further characterize the mutant strains, your advisor recommends that you first
         analyze the mutant strains' DNA content by flow cytometry. While there are other more cost-prohibitive ways to
         characterize cell cycle mutants, using expensive reagents, such as antibodies, she would like to keep costs low.
         She hopes that the results of the DNA content analysis will provide the necessary data to further characterize
         these cell cycle mutants and determine the arrest point at which the mutant strains are arresting.
-        </p>
         <p>
         Perform a flow cytometry experiment(s) to further characterize the Mutant 1 and Mutant 2 strains. Based on your
         flow cytometry results and analysis, which cell cycle arrest point(s) are responsible for the phenotype you
@@ -79,14 +78,14 @@
         <div>2</div>
     </div>
     <div class='scb_objective_text'>
-        <p>
+
         You present your flow cytometry experiment results and analyses to your faculty
         advisor. She suggests that it will be beneficial to conduct other experiments to further characterize the mutant
         strains. She urges you to perform western blotting to determine the protein levels and mobility of key cell
         cycle proteins in the mutant strains when grown at the restrictive temperature and allows you to purchase many
         antibodies to complete a thorough western blotting analysis. See the <b>Reference Information</b> (below) for more
         information about these antibodies.
-            </p><p>
+            <p>
         Perform a western blotting experiment(s) to further characterize the cell cycle defects in the Mutant 1 and
         Mutant 2 strains. Based on your western blotting results, which cell cycle arrest point(s) are responsible for
         the phenotype you observe for the Mutant 1 and Mutant 2 strains? For each mutant strain, describe how the
@@ -119,12 +118,12 @@
             experiments.
         </li>
         <li>
-            Chemical treatments. a) Cell cycle specific drugs that provide known, expected results under appropriate
+            Chemical treatments. <br>a) Cell cycle specific drugs that provide known, expected results under appropriate
             conditions to which you may compare your experimental samples involving the mutant strains. The drugs are:
             alpha factor = a mating pheromone, which results in a cell cycle arrest in G1; hydroxyurea = a drug that
             depletes the cell of deoxyribonucleotides (dNTPs), which results in a cell cycle arrest in S-phase; and
             nocodazole = a drug that inhibits polymerization of microtubules, which results in a cell cycle arrest in
-            mitosis. b) Protein Phosphatase 1 (PP1) = a phosphatase enzyme that removes phosphate groups from all
+            mitosis. <br>b) Other drugs. Protein Phosphatase 1 (PP1) = a phosphatase enzyme that removes phosphate groups from all
             phosphorylated-serine, -threonine and -tyrosine amino acids.
         </li>
         <li>
@@ -175,8 +174,6 @@
                 </tbody>
 
             </table>
-        </li>
-    </ol>
     <p>
         For these experiments in StarCellBio you can assume that all of these antibodies recognize the phosphorylated
         and
@@ -193,6 +190,8 @@
         cleavage sites:<br>
         <img src='/static/assignments/mit706s13/assets/cleavage_sites.png'>
     </p>
+        </li>
+    </ol>
 
 
 </div>

html_app/assignments/tufts/gen/instructions.gss.css

@@ -1,15 +1,18 @@
 .scb_s_tufts_assignment_overview {
   font-family: 'SourceSansPro-Regular';
   font-size: 12pt;
+  text-align: left;
 }
 .scb_assignment_specific_tufts_experiment_setup {
   font-family: 'SourceSansPro-Regular';
   font-size: 10pt;
+  text-align: left;
 }
 .scb_assignment_specific_tufts_experiment_setup>li>b {
   font-family: 'SourceSansPro-Semibold';
 }
 .scb_s_tufts_assignment_detail {
   font-family: 'SourceSansPro-Regular';
   font-size: 12pt;
+  text-align: left;
 }