Team:HokkaidoU Japan/Notebook

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{{Team:HokkaidoU_Japan/header}}
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!align="center"|[[Team:HokkaidoU_Japan|Home]]
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{{Team:HokkaidoU_Japan/nav.notebook}}
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!align="center"|[[Team:HokkaidoU_Japan/Team|Team]]
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<div id="hokkaidou-column-main">
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!align="center"|[https://igem.org/Team.cgi?year=2012&team_name=HokkaidoU_Japan Official Team Profile]
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<!-- DO NOT EDIT OVER THIS LINE @iTakeshi -->
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!align="center"|[[Team:HokkaidoU_Japan/Project|Project]]
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!align="center"|[[Team:HokkaidoU_Japan/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:HokkaidoU_Japan/Modeling|Modeling]]
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    .hokkaidou-notebook-index {
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!align="center"|[[Team:HokkaidoU_Japan/Notebook|Notebook]]
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!align="center"|[[Team:HokkaidoU_Japan/Safety|Safety]]
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!align="center"|[[Team:HokkaidoU_Japan/Attributions|Attributions]]
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== Hello ==
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We are team HokkaidoU Japan! Today we learn and start to edit wiki.
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(>ω<)　<br>
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        border-radius: 1em;
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Dear Mr.Ortiz, I saw the help page which you edited.<br>
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    }
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hola!<br>
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    .hokkaidou-notebook-index h5 {
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==March==
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===Spring Boot Camp===
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;date
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:March 5 (Mon) ~ March 9 (Fri)
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    .hokkaidou-notebook-index h5 {
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====Monday, March 5====
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        color:white;
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;Session #1
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:Short lecture about moleculer biology (Mr.Yamazaki, our adviser)
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    .hokkaidou-notebook-index:hover p {
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;Session #2
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:Tutrial: How to use 'Unipro UGENE' (iTakeshi)
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    }
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;Session #3
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    .hokkaidou-notebook-index p {
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:Guidance: Wiki Reading (Laury)
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        font-size:12px;
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::Example: 2010 MIT
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        width:500px;
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====Tuesday, March 6====
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        line-height:1.5;
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;Session #4~6
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        color: #ffffff;
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:Reading Wikis in turn and discussions
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    }
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:*2010 NYU
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    .hokkaidou-notebook-index:hover {
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:*2009 Cambridge
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        background-position:200px 50%;
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:*2009 Growningen
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    }
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====Wednesday, March 7====
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    #hokkaidou-notebook-bootcamp {
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;Session #7~11
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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:Reading Wikis (2)
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        background-position: 673px -522px;
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:*2010 Washington
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    }
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:*2009 Valencia
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    #hokkaidou-notebook-bootcamp:hover {
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:*2011 Barklay
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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:*2010 Paris
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        background-position: 543px -522px;
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:*2010 Bristol
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    }
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====Thursday, March 8====
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    #hokkaidou-notebook-diary {
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;Session #12
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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:2012 Project Brainstorming
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        background-position: 673px -653px;
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::The details is secret! :)
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    }
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;Session #13
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    #hokkaidou-notebook-diary:hover {
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:Guidance: How to read papers (Laury)
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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====Friday, March 9====
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        background-position: 543px -653px;
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;Session #14
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    }
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:2012 Project Brainstorming (2)
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    #hokkaidou-notebook-protocols {
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;Session #15
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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:Guidance: How to look up papers you want (Laury)
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        background-position: 673px -783px;
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;Session #16
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    }
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:Tutorial: Modeling the behavior of cells (iTakeshi)
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    #hokkaidou-notebook-protocols:hover {
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;Session #17
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        background-image: url('https://static.igem.org/mediawiki/2012/e/ea/HokkaidoU2012_Menu_Circle.png');
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:Final Session: Reviewing this camp
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;Party!!
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    }
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</style>
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==Experiment Calender==
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<h2>Notebook</h2>
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{|class="calendar"
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<div class="hokkaidou-section">
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|-
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<a href="/Team:HokkaidoU_Japan/Notebook/Spring_Boot_Camp" class="hokkaidou-notebook-index" id="hokkaidou-notebook-bootcamp">
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|colspan="7"|July
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  <h5>Boot Camp</h5>
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|-
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  <p>Be my apprentice.</p>
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!style="color:red;"|S
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</a>
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!M
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<a href="/Team:HokkaidoU_Japan/Notebook/Lab_Diary" class="hokkaidou-notebook-index" id="hokkaidou-notebook-diary">
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!T
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  <h5>Lab Diary</h5>
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!W
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  <p>That's one small step for you, one giant leap for us. </p>
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!T
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</a>
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!F
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<a href="/Team:HokkaidoU_Japan/Notebook/overall_protocols" class="hokkaidou-notebook-index" id="hokkaidou-notebook-protocols">
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!style="color:blue;"|S
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  <h5>Protocols</h5>
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|-
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  <p>Bible of our lab.</p>
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|style="color:red;"|1
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</a>
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|2
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</div>
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|3
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|4
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<!-- DO NOT EDIT UNDER THIS LINE @iTakeshi -->
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|&nbsp;
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=July=
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==phaABC team==
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now experimenting...
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==Ag43&Lysis team==
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===weak 1(4th~10th)===
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*4th
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;Transformation
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-
Transformation of BBa_B0015(dT), B0034(RBS), I179005(pT7), K346007(Ag43), and K542009(pLacI-RBS-Ag43) in DH5α
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-
#Added each DNA solutions (1ul) into DH5α comeptent cell and standed on ice in 30 min.
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-
#Cultivated on LBA(dt,RBS,T7) and LBC(Ag43, pLacI-RBS-Ag43). E.coli cultivate in  LBC was pre-cultivated in 2 hrs. pT7 was 21hrs and Others were 20hrs cultivated
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-
<br>
+
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+
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*5th
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;Transformation
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K346007(Ag43) was failed to cultivate on LBC plate.
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Transformation of K346007(Ag43) in DH5α.
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#Add DNA solution(1ul) into DH5α comeptent cell and stand on ice in 30 min.
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#Pre-cultivated in 2hrs.
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#Cultivated on LBC in 21hrs.
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-
 
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;Single colony isolation
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Single colony isolation of BBa_B0015, B0034, I179005 and K542009.
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#Picked up one colony.
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#Cultivation on LBA(dt,RBS,T7) and LBC(pLacI-RBS-Ag43) in 14hrs30mins
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BBa_K542009 was Ag43 only part! And the part didn't have Biobrick suffix.
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-
 
+
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*6th
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;Liquid culture
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Liquid culture in LBA(dT,RBS,pT7) and LBC(pLacI-RBS-Ag43)
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#Picked up two colonies from each plates.
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#One colony was dipped in 1ml LB (A or C), and other colony was dipped in 2ml LB(A or C). 1ml is for glycerol stocks and 2ml is for mini-prep.
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#16hrs Cultivation
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<br>
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;Single colony isolation
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#Single colony isolation of K346007(Ag43).
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<br>
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*7th
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;Liquid culture
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Liquid culture in LBC(Ag43).
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#Picked up two colonies from each plates.
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#Both of colonies were dipped in 2ml LBC, and then we cultivate them in 38℃.<br>
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However, one of them cultivated only 8 hours. It's for glycerol stock.
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<br>
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'''3A assembly!'''<br>
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Assembled pT7, RBS and pSB1C3 by 3A assembly.
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This 3A assembly is our first try!
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;mini-prep
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#mini-prep of dT,RBS,pT7 and pLacI-RBS-Ag43.
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#Elution in 50ul buffer
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<br>
+
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;Glycerol stock
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Made glycerol stocks of dT,RBS,pT7 and pLacI-RBS-Ag43.
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#Parts written above were cultivated in LBA(dT,RBS,pT7) and LBC(pLacI-RBS-Ag43) 1ml in 16hrs 30min.
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#Add glycerol and Freeze at -80C
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<br>
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[[Image:120707_I719005_B0034_B0015_K542009_mini-prep_umeuchi.jpg]]
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;Electrophoresis
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Electrophoresis to predict concentration of mini-prep products(dT,RBS,pT7 and pLacI-RBS-Ag43).
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#Used 1% agarose gel.
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#Pre-migration.
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#Migrated 1.2ul of DNA solutions (1ul is mini-prep products and 0.2ul is Loading Dye) in 35min.
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#Took a photograph of 1% agarose gel that finished electrophoresis.
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<br>
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;Digestion
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<br>
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Digestion of I719005, B0034 and pSB1K3
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Digestion recipe
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All parts were reacted in 30ul solution.
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*I719005(40ng/ul)
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{|
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|DNA solution
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|12.5ul
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|-
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|EcoRI
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|1ul
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|-
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|SpeI
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|1ul
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|-
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|10xH Buffer
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|3ul
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|-
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|DW
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|12.5ul
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|}
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*B0034(40ng/ul)
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{|
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|DNA solution
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|12.5ul
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|-
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|XbaI
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|1ul
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|-
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|PstI
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|1ul
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|-
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|10xM Buffer
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|3ul
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|-
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|DW
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|12.5ul
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|}
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*pSB1K3(25ng/ul)
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{|
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|DNA solution
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|12ul
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|-
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|EcoRI
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|1ul
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|-
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|PstI
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|1ul
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|-
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|10xH Buffer
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|3ul
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|-
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|DW
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|13ul
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|}
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<br>
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;Ethanol precipitation
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For rising concentration of DNA solution which use for Ligation and removing restriction enzyme.
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#Added 3ul of NaoAC, 1.5ul of glycogen and 75ul of 100% ethanol.
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#Centrifuged in 14000rpm, 30min at 4C.
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#Remove supernatant and added 220ul of 70% ethanol.
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#Centrifuged in 15000rpm, 15min at 4C.
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#Remove supernatant and air drying in room temperature then added 10ul of DW.
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<br>
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;Ligation
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All DNA solutions were digested.
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3A assembly protocol required Ligation reaction should be in total 25ul solution.
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{|
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|Ligation Mighty Mix
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|12.5ul
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|-
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|pT7
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|2ul
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|-
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|RBS
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|2ul
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|-
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|pSB1K3
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|2ul
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|-
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|DW
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|6.5ul
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|-
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|――――――――――
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|-
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|Total
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|25ul
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-
|}
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Ligation reaction recipe was written below.
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-
 
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{|
+
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|Degree
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|Minute
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-
|-
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|16
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|30
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|-
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|65
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|10
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-
|-
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|4
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|Hold
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-
|}
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<br>
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ligation was finished.
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But now pm10:00.  2.5hrs needs for doing transformation. Transformation would finish at am:0:30.
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-
 
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Withdraw!!!!
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+
-
 
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*8th
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*(pT7 + RBS)
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;Transformation
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Transformation for pT7+RBS+pSB1K3
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-
#Added DNA soltions (Ligation products) 1ul to DH5α compitent cell.
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#Stood on ice in 30min.
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#Added 600ul of LB to transformed DH5α solution.
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#Pre-cultivate in 2hrs
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#Splead 300ul of LB&DH5α solution to LBA.
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#Cultivated in OOhrs. 
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-
<br>
+
-
 
+
-
*K346007(Ag43)
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;mini-prep
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mini-prep for Liquid culture product of K346007(Ag43)
+
-
#Used FastGene Plasmid Mini Kit(Nippon Genetics)
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-
#Elutioned in 50ul
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-
#First we eluted in colection tube. then moved in Eppendorf tube.
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-
 
+
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;Erectrophoresis
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Erectrophoresis for mini-prep product(Ag43).
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#Prepared 1% Agalose gel and added EtBr then pre-migration in 30min.
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-
#1ul 1kb ladder, 1.2ul mini-prep product(1ul is DNA solution and 0.2ul is loading dye) added then migtrated
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-
 
+
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*(Ag43 + dT)
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Assembling K346007(Ag43) + B0015(dT) with 2-piece assembly(Biobrisk standard assembly)
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;Digestion
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-
Digested Ag43 and dT in solution recipe Written below
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-
*Ag43(Insert)
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5190bp
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{|
+
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|DNA solution
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|48ul
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-
|-
+
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|EcoRI
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|1ul
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-
|-
+
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|SpeI
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|1ul
+
-
|-
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|10xH buffer
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|6ul
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-
|-
+
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|DW
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|4ul
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-
|-
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|――――――――――――
+
-
|-
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|Total
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|60ul
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-
|}
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-
 
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*dT(Vector)
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3318bp
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{|
+
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|DNA solution
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|8ul
+
-
|-
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|EcoRI
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|1ul
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-
|-
+
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|XbaI
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|1ul
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-
|-
+
-
|10xM buffer
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-
|2ul
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-
|-
+
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|DW
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|8ul
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-
|-
+
-
|――――――――――――
+
-
|-
+
-
|Total
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-
|20ul
+
-
|}
+

Latest revision as of 00:52, 27 September 2012

Notebook

Boot Camp

Be my apprentice.
Lab Diary

That's one small step for you, one giant leap for us.

Protocols

Bible of our lab.


Retrieved from "http://2012.igem.org/Team:HokkaidoU_Japan/Notebook"