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- | <h1>Lab Notes - July</h1>
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- | <h1>Biobrick Group</h1>
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- | | + | |
- | <h1>Week1</h1>
| + | |
- | <table id="notesheet" border="1" cellspacing="0"
| + | |
- | cellpadding="1" style="vertical-align: middle">
| + | |
- | <tr>
| + | |
- | <td width="76"><strong>Day</strong></td>
| + | |
- | <td width="349"><strong>Note</strong></td>
| + | |
- | </tr>
| + | |
- | | + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.4th Monday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="328" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- |
| + | |
- | <td width="128">▪ Aerobic cultivation of DH5α</td>
| + | |
- | | + | |
- | | + | |
- | <td width="196">▪ Preparation of apparatus for the formation of
| + | |
- | biofilm</td>
| + | |
- | | + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul 5th Tuesday</td>
| + | |
- | <td> </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.6th Wednesday</td>
| + | |
- | <td>
| + | |
- | <table width="217" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="215">▪ Receiving primers ordered previously</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.7th Thursday</td>
| + | |
- | <td>
| + | |
- | <table width="238" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="200">▪ Preparation of the aliquot of the primers</td>
| + | |
- | <td width="200">▪ Something wrong with a shaking incubator</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.8th Friday</td>
| + | |
- | <td>
| + | |
- | <table width="222" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="155">▪ Preparation of culture plates for the
| + | |
- | transformations</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.9th Saturday</td>
| + | |
- | <td>
| + | |
- | <table width="313" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="127">▪ Preparation of culture plates for the
| + | |
- | transformations</td>
| + | |
- | <td width="182">▪ protocols of transformation</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.10th Sunday</td>
| + | |
- | <td>
| + | |
- | <table width="246" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>▪ Several colonies were picked up and cultivated in 5mL LB
| + | |
- | medium. ▪ryosectioning of biofilm</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | | + | |
- | </table>
| + | |
- | </p>
| + | |
- | <h1>Week2</h1>
| + | |
- | <table id="notesheet" width="650" border="1" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="76"><strong>Day</strong></td>
| + | |
- | <td width="349"><strong>Note</strong></td>
| + | |
- | </tr>
| + | |
- | | + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.11th Monday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="541" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="128">▪ Set up new LB culture plates with ampicillin
| + | |
- | and kanamycin
| + | |
- | </p>
| + | |
- | </td>
| + | |
- | | + | |
- | | + | |
- | <td width="196">▪ Sterilization of Glycerol and <br />
| + | |
- | Preparation of 25mg/mL kanamycin</td>
| + | |
- | <td>▪Transformation of the parts mentioned on Jul.9th for the
| + | |
- | second time</td>
| + | |
- | <td>▪Observation the sections</td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul 12th Tuesday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="560" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="128">▪ Pick two colonies of each parts and cultivate
| + | |
- | them in LB medium</td>
| + | |
- | | + | |
- | | + | |
- | <td width="203">▪ Transformation of three parts(20J,20H.22B from
| + | |
- | Kit plates of 2011 Distribution ) which are related to the
| + | |
- | degradation of Cellulose</td>
| + | |
- | <td width="91">▪Min prep to isolate 10I,12I and 22M</td>
| + | |
- | <td width="130">▪Conservation of 10I,12I,22M and 11P</td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.13th Wednesday</td>
| + | |
- | <td>
| + | |
- | <table width="618" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="104">▪ Place the culture plate of 20J,20H and 22B in
| + | |
- | the fridge.</td>
| + | |
- | <td width="102">▪min prep to isolate 13K ▪onservation of 13K</td>
| + | |
- | <td width="163">▪estriction digest of the
| + | |
- | parts(12I,10I,22M,13K) with EcoRI and PstI</td>
| + | |
- | <td width="111">▪Gel electrophoresis to analyse restriction
| + | |
- | fragments</td>
| + | |
- | <td width="128">▪Test the Tm of Primers CP1&CS,NP&NS
| + | |
- | with 13K. The result of Gel electrophoresis shows that 60.2℃ is the
| + | |
- | Tm of NS and NP, and 57.4℃ is the Tm of CS and CP1.</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.14th Thursday</td>
| + | |
- | <td>
| + | |
- | <table width="618" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>▪ Test the Tm of the YFP,RFP,tetR,Vgb and nirB primers.
| + | |
- | The result of Gel electrophoresis shows that the Tm for the primers
| + | |
- | of Vgb is 54℃ and the Tm for the primers of nirB is 55℃ The RCR of
| + | |
- | YFP,RFP and tetR failed.</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.15th Friday</td>
| + | |
- | <td>
| + | |
- | <table width="600" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="155">▪ PCR(Phusion)<br />
| + | |
- | ▪ Digest 10I, 22M, 13K ▪ Used wrong cutter, digestion again.</td>
| + | |
- | <td>▪ Run the results of PCR and the first digestion. The
| + | |
- | annealing temperature of YFP needed change. The digestion results
| + | |
- | confirmed</td>
| + | |
- | <td>▪ Run the digestion results of second time. The bands are
| + | |
- | confirmed.</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.16th Saturday</td>
| + | |
- | <td>
| + | |
- | <table width="620" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="127">▪ Cut the linearized pSB1k3 with E+P</td>
| + | |
- | <td width="123">▪ Purify the digestion results of 22M, 13K, 10I</td>
| + | |
- | <td width="133">▪ Confirm digestion of pSB1k3 by
| + | |
- | electrophoresis, then purification</td>
| + | |
- | <td width="113">▪ Test Tm of YFP<br />
| + | |
- | ▪ ligation: 22M+10I, 13K+10I</td>
| + | |
- | <td width="114">▪ Tm of YFP is 54 degree ▪ transform the
| + | |
- | ligation results.</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.17th Sunday</td>
| + | |
- | <td>
| + | |
- | <table width="620" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>▪ PCR 22M<br />
| + | |
- | ▪ purify Vgb, RFP, RFP-tetR, YFP-tetR. Gibson PCR.</td>
| + | |
- | <td>▪ ligation the purified the fragments in yesterday.</td>
| + | |
- | <td>▪ 22M PCR<br />
| + | |
- | ▪ Transform the ligation results.</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | | + | |
- | </table>
| + | |
- | | + | |
- | <p> </p>
| + | |
- | <h1>Week3</h1>
| + | |
- | <table id="notesheet" width="713" border="1" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="87"><strong>Day</strong></td>
| + | |
- | <td width="616"><strong>Note</strong></td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.18th Monday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="541" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="128">▪ Genome extraction of E.coli</td>
| + | |
- | | + | |
- | | + | |
- | <td width="196">▪ PCR of NirB<br />
| + | |
- | ▪ Cut 10I with X+P, cut 22M, 13K with E+S, cut pSB1k3 with E+P</td>
| + | |
- | <td>▪ Ligate: 10I+13K, 10I+22M <br />
| + | |
- | ▪ Repeat NirB PCR</td>
| + | |
- | <td>
| + | |
- | <p align="left">▪ Culture 11P<br />
| + | |
- | ▪ Miniprep 10I, 22M, 13K</p>
| + | |
- | </td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul 19th Tuesday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="615" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="140">▪ mini-prep: 10I+13K, 10I+22M</td>
| + | |
- | | + | |
- | | + | |
- | <td width="213">▪Insert 10I+13K, 10I+22M into pSB1k3</td>
| + | |
- | <td width="110">▪Transform: 5E, 3C, 7C, 1K, 1I from the
| + | |
- | distribution plate</td>
| + | |
- | <td width="144">▪Transform 10I+22M, 10I+13K</td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.20th Wednesday</td>
| + | |
- | <td>
| + | |
- | <table width="610" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="170">▪Colonies of 22M+10I, 13K+10I, 5E, 3C, 7C, 1K,
| + | |
- | 1I confirmed</td>
| + | |
- | <td width="102">▪ Gibson PCR</td>
| + | |
- | <td width="250">▪Colony PCR 22M+10I, 13K+10I, 5E, 3C, 7C, 1K,
| + | |
- | 1I</td>
| + | |
- | <td width="80">▪PCR NirB</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.21th Thursday</td>
| + | |
- | <td>
| + | |
- | <table width="618" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>▪PCR verification of 22M+10I, 13K+10I, 5E, 3C, 7C, 1K, 1I
| + | |
- | </td>
| + | |
- | <td>▪ Gibson PCR ▪ Run the results of PCR verification. Bands
| + | |
- | confirmed.</td>
| + | |
- | <td>▪ Culture the 22M+10I, 13K+10I, 5E, 3C, 7C, 1K, 1I ▪
| + | |
- | Purification of Gibson PCR results</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.22th Friday</td>
| + | |
- | <td>
| + | |
- | <table width="618" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="117">▪ PCR amplification of Gibson assembly results
| + | |
- | </td>
| + | |
- | <td width="144">▪ Mini prep: 22M+10I, 22.Presever in -20<br />
| + | |
- | ▪ Mini prep: 1K,1I,3C,5E,7C<br />
| + | |
- | ▪ Gibson Assembly fail.</td>
| + | |
- | <td width="164">▪ PCR NirB by Phusion<br />
| + | |
- | ▪Repeat PCR by changing Pnibr to Gnirbr<br />
| + | |
- | ▪Cut the mini and medi prep results with E</td>
| + | |
- | <td width="185">▪ Run the results of PCR and digestion. Fail in
| + | |
- | PCR of NirB, succeed in 10I+3K and 10I+22M ligation.</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.23th Saturday</td>
| + | |
- | <td>
| + | |
- | <table width="613" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="237">▪Double digestion of 13K+10I, 22M+10I, pSB1c3
| + | |
- | | + | |
- | </td>
| + | |
- | <td width="169">▪ Fail in purification of Medi prep</td>
| + | |
- | <td width="201">▪ PCR NirB<br />
| + | |
- | ▪ Ligate NirB+13K+10I, Vgb+22M+10I</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.24th Sunday</td>
| + | |
- | <td>
| + | |
- | <table width="608" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="244">▪ Gibson assembly: NirB+RFP+tetR<br />
| + | |
- | ▪ Cut results of Gibson assembly and pSB1c3.</td>
| + | |
- | <td width="164">▪ Purify the ligation results in yesterday</td>
| + | |
- | <td width="194">▪ ligate with backbone ▪ Culture 1I, 1K, 3C,
| + | |
- | 5E, 7C, 11P</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | | + | |
- | </table>
| + | |
- | <p> </p>
| + | |
- | <h1>Week4</h1>
| + | |
- | <table id="notesheet" width="691" border="1" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="63"><strong>Day</strong></td>
| + | |
- | <td width="630"><strong>Note</strong></td>
| + | |
- | </tr>
| + | |
- | | + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.25th Monday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="541" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="128">▪ Transform Pnirb+13k+10I+pSBK3-2</td>
| + | |
- | | + | |
- | | + | |
- | <td>▪ Place the culture in 4 degree</td>
| + | |
- | <td>▪ Medi-and mini-prep of five cultre</td>
| + | |
- | <td>▪Gibson Assembly confirmation by gel</td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul. 26th Tuesday</td>
| + | |
- | <td>
| + | |
- | <table id="intable" width="610" border="0" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | | + | |
- | <td width="134">▪ Cut Pnirb, Pvgb,(E+S)<br />
| + | |
- | ▪ Cut 10I+13K, 10I+22M.(X+P)</td>
| + | |
- | | + | |
- | | + | |
- | <td width="167">▪ Ligation: vgb+10I+22M, nirB+10I+13K,</td>
| + | |
- | <td width="172">▪ Ligation: pSBK13+vgb+10I+22M,
| + | |
- | pSBK13+nirB+10I+13K</td>
| + | |
- | <td width="129">▪ Transform the ligation results.</td>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.27th Wednesday</td>
| + | |
- | <td>
| + | |
- | <table width="608" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="170">▪ No colony on the plate<br />
| + | |
- | ▪ Gibson assembly</td>
| + | |
- | <td width="184">▪ Run the results of Gibson assembly</td>
| + | |
- | <td width="248">▪ Excise the bands, the purify the DNA<br />
| + | |
- | ▪ Gibson Assenmly</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.28th Thursday</td>
| + | |
- | <td>
| + | |
- | <table width="609" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="607">▪ 2011 China Meet-up @ Hefei</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.29th Friday</td>
| + | |
- | <td>
| + | |
- | <table width="607" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>▪ 2011 China Meet-up @ Hefei</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.30th Saturday</td>
| + | |
- | <td>
| + | |
- | <table width="620" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | | + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td id="sheetleft">Jul.31th Sunday</td>
| + | |
- | <td>
| + | |
- | <table width="600" border="0" cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td width="368">▪ Culture 22M+10I, 13K+10I</td>
| + | |
- | <td width="228">▪ Cut a0H, 20J, 22B</td>
| + | |
- | | + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </td>
| + | |
- | </tr>
| + | |
- | | + | |
- | </table>
| + | |
- | <br />
| + | |
- | <br />
| + | |
- | </div>
| + | |
- | <!--page1-->
| + | |
- | <div id="importantcontainer">
| + | |
- | <div class="frame" id="important">
| + | |
- | <div class="bgcolors" id="round">
| + | |
- | <h1>Data/Protocol</h1>
| + | |
- | </div>
| + | |
- | </div>
| + | |
- | </div>
| + | |
- | <div id="framecontent">
| + | |
- | <h1>Jul.13th Wednesday</h1>
| + | |
- | | + | |
- | <p><strong>Systems of restriction digestion with EcoRI and
| + | |
- | PstI</strong></p>
| + | |
- | <p>
| + | |
- | <table style="margin: 15px;" width="110" height="200" border="1"
| + | |
- | cellspacing="0" cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>Plasmid</td>
| + | |
- | <td>1μL (>100ng)</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>EcoRI</td>
| + | |
- | <td>1μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>PstI</td>
| + | |
- | <td>1μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>10×Buffer Tango</td>
| + | |
- | <td>2μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>ddH2O</td>
| + | |
- | <td>15μL</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | <img src="https://static.igem.org/mediawiki/2011/c/c3/0713program.png"
| + | |
- | width="200" height="200" /></p>
| + | |
- | <p><strong>Temperature grad</strong><br />
| + | |
- | 56℃ 57.4℃ 60.2℃ 62.9℃ 64.3℃ 65.8℃ /p>
| + | |
- | <div id="framecontent">
| + | |
- | <p> </p>
| + | |
- | | + | |
- | <p><strong>PCR system (test the Tm of the primers
| + | |
- | CP1&CS, NP&NS)</strong></p>
| + | |
- | | + | |
- | <table style="margin: 15px;" width="110" border="1" cellspacing="0"
| + | |
- | cellpadding="1">
| + | |
- | <tr>
| + | |
- | <td>10×Buffer</td>
| + | |
- | <td>2μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>dNTPs</td>
| + | |
- | <td>0.5μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>primers CP1 (NP)</td>
| + | |
- | <td>1μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>primers CS (NS)</td>
| + | |
- | <td>1μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>Template</td>
| + | |
- | <td>1μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>rTaq</td>
| + | |
- | <td>0.2μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>H2O</td>
| + | |
- | <td>14.5μL</td>
| + | |
- | </tr>
| + | |
- | <tr>
| + | |
- | <td>Total</td>
| + | |
- | <td>20μL</td>
| + | |
- | </tr>
| + | |
- | </table>
| + | |
- | </p>
| + | |
- | <p>Within each compartment are<strong> components</strong>: include
| + | |
- | different types of biomass ,substrates , products. biomass is often
| + | |
- | divided into active microbial species, inert cells, and extracellular
| + | |
- | polymeric substances(EPS).</p>
| + | |
- | <p>The components can undergo transformation, transport, and
| + | |
- | transfer <strong>processes</strong>. For example, substrate is consumed,
| + | |
- | and this leads to the synthesis of new active biomass.</p>
| + | |
- | <p>All process affecting each component in each compartment are
| + | |
- | mathematically linked together into a<strong> mass balance
| + | |
- | equation</strong> that contains rate terms and parameters for each process.</p>
| + | |
- | <p><strong>Model Selection:</strong>Many kinds of Mathematics models
| + | |
- | have been founded to describe a system of biofilm. Models of different
| + | |
- | dimensions (1d, 2d, 3d) focus on different properties of a biofilm.
| + | |
- | Since we care most about the oxygen concentration gradients
| + | |
- | perpendicular to the substratum, <strong>numerical
| + | |
- | 1-dimensional dynamic model(N1)</strong> would be a proper choice for us.</p>
| + | |
- | </div>
| + | |
- | <!--bgcolors--></div>
| + | |
- | <!--important--></div>
| + | |
- | <!--importantcontainer-->
| + | |
- | <p style="clear: both;"></p>
| + | |
- | <div id="page2">
| + | |
- | <div class="block" id="nsheet"><img
| + | |
- | src="http://ung.igem.org/wiki/images/4/42/Biofilmcomp.png" width="640"
| + | |
- | height="464" style="margin: 5px;" />
| + | |
- | <p> </p>
| + | |
- | </div>
| + | |
- | <div class="block" id="nsheet">
| + | |
- | <h1>Early July</h1>
| + | |
- | <p>Pre-experiments with biofilm formation with circular and non
| + | |
- | circular silicone tube, 24 well plate on different support including
| + | |
- | glass, paper, plastic film, rubber. The final material are used based on
| + | |
- | the easiness biofilm form on them and on the easiness to observe under
| + | |
- | microscope.</p>
| + | |
- | <img
| + | |
- | src="https://static.igem.org/mediawiki/2011/b/be/20110711-3nP4100X0877.jpg"
| + | |
- | width="400" style="margin-left: 20px;">
| + | |
- | <p> </p></div>
| + | |
- | <div class="block" id="nsheet">
| + | |
- | <h1>28th July</h1>
| + | |
- | <p>13.30: DH5α 11p 5mlX4<br />
| + | |
- | 23.00: silicone tube set at 37℃ /p>
| + | |
- | </div>
| + | |
- | <div class="block" id="nsheet">
| + | |
- | <h1>29th July</h1>
| + | |
- | <p>13.00: LB culture 50ml with circular culture medium. LB culture
| + | |
- | 50ml with noncircular culture medium.</p>
| + | |
- | | + | |
- | </div>
| + | |
- | <div class="block" id="nsheet">
| + | |
- | <h1>31st July</h1>
| + | |
- | <p>13.00: -80℃ storing silicone tube. A thick white and loosely bond
| + | |
- | substance is seen on the inner wall of the 5mm silicone tube, and on the
| + | |
- | inner wall of the 1mm silicone tube a flatter and smoother white
| + | |
- | substance. Especially obvious where the tube turns. Possibly because the
| + | |
- | speed of culture flow is slower.</p>
| + | |
- | | + | |
- | </div>
| + | |
- | </div>
| + | |
- | <!--page2--> <script type="text/javascript">
| + | |
- | document.getElementById('bb').onclick= function(){
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- | document.getElementById('page2').style.display='none'
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- | document.getElementById('page1').style.display='block'}
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- | document.getElementById('bf').onclick= function(){
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- |
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- | document.getElementById('page1').style.display='none'
| + | |
- | document.getElementById('pgae2').style.display='block'}
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- | </script>
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- | <p style="clear: both"></p>
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- | </div>
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- | <!--framecontent-->
| + | |
- | | + | |
- | <div style="display: none" class="frame" id="rightnav">
| + | |
- | <div class="bgcolors" id="round">
| + | |
- | <p><a name="jumptop" id="bb"> Biobrick Group </a>|<a
| + | |
- | id="bf"> Biofilm Group </a></p>
| + | |
- | </div>
| + | |
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| + | |
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