Team:Todai-Tokyo/Protocols/Notebook Sample
From 2009.igem.org
(New page: {{:Team:Todai-Tokyo/Template}} {| width="100%" cellpadding="0px" cellspacing="5px" style="font-family:'Century Gothic', sans-serif;" |- style="background:#BC8F8FF; height:100px;" valign="...) |
|||
(12 intermediate revisions not shown) | |||
Line 6: | Line 6: | ||
<html> | <html> | ||
+ | <font size = 4><B>このページの使い方</b></font><BR><BR> | ||
+ | 各メソッドのサンプルです。<BR> | ||
+ | ソース(edit画面)からそれぞれをコピーして使いたいところに貼り付け、必要なところを変える。<BR> | ||
+ | *このページに登場する作業やDNA配列はフィクションです。<BR><BR> | ||
- | <h2> Miniprep <h2> | + | |
- | <h2> PCR <h2> | + | </html> |
- | <h2> Sequencing <h2> | + | |
- | <h2> Transformation <h2> | + | <h2> Miniprep </h2> |
- | <h2> Ligation <h2> | + | |
- | <h2> Infusion <h2> | + | The following were [[Team:Todai-Tokyo/Protocols/Miniprep|miniprep]]ped: |
- | <h2> Gel Purification <h2> | + | |
- | <h2> | + | * pLacI-RFP-dterm (From Ligation on 9/4): 4 colonies |
+ | * RFP ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J04450 BBa_J04450] from [http://partsregistry.org/assembly/libraries.cgi?id=19 2009 Spring Distribution]): 6 colonies | ||
+ | |||
+ | |||
+ | <h2> PCR </h2> | ||
+ | |||
+ | The yqiT gene was [[Team:Todai-Tokyo/Protocols/PCR|PCR]] amplified from pLacI-yqiT-dterm ([[Team:Todai-Tokyo/Protocols/Miniprep|miniprep]]ped on 9/7) using the following primers: | ||
+ | |||
+ | '''yqiT fwd''': agcccgtgtagtactgtagagtt <BR> | ||
+ | '''yqiT rev''': agggatgtttgccagtcgtaattag <BR> | ||
+ | |||
+ | using [[Team:Todai-Tokyo/Protocols/PCR/programs|PCR program 1]] and [[Team:Todai-Tokyo/Protocols/PCR/Enzymes|Ex-taq]]. | ||
+ | |||
+ | Note: This PCR reaction attaches a Biobrick prefix and suffix to the gene. | ||
+ | |||
+ | *補足: Program 1と書いてあるところは、いつも使うようなプログラムと違うものを使ってそれを記したい場合はプログラムの内容をリンク先に書き込みましょう。わからない場合は聞いてください。 | ||
+ | |||
+ | |||
+ | <h2> Sequencing </h2> | ||
+ | |||
+ | The following were [[Team:Todai-Tokyo/Protocols/sequencing|sequenced]] using the labeled primers: | ||
+ | |||
+ | * pAraC Sample 1 ([[Team:Todai-Tokyo/Protocols/Miniprep|miniprep]]ped on 9/23) | ||
+ | ** 1) '''Biobrick vector fwd''': atatgagagcgcgcgcagagagagatg | ||
+ | ** 2) '''Biobrick vector rev''': tttttaaaagggggtgtgtgtgtaaagttt | ||
+ | * pAraC Sample 2 ([[Team:Todai-Tokyo/Protocols/Miniprep|miniprep]]ped on 9/23) | ||
+ | ** 3) '''Biobrick vector fwd''': atatgagagcgcgcgcagagagagatg | ||
+ | <BR> | ||
+ | |||
+ | '''Results''':<BR><BR> | ||
+ | 1) Sequence read failed | ||
+ | <BR>2) Single-base mutation found in sequence that creates stop codon; re-do the ligation | ||
+ | <BR>3) Desired Sequence read | ||
+ | |||
+ | |||
+ | <h2> Transformation </h2> | ||
+ | |||
+ | The following were [[Team:Todai-Tokyo/Protocols/Transformation|Transformed]] into ''E. coli'' competent cells: | ||
+ | |||
+ | * pAraC-RBS ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J04451 BBa_J04451] from [http://partsregistry.org/assembly/libraries.cgi?id=19 2009 Spring Distribution]) | ||
+ | * pLacI ([[Team:Todai-Tokyo/Protocols/Miniprep|miniprep]]ped on 9/23) | ||
+ | |||
+ | |||
+ | <h2> Ligation + Transformation </h2> | ||
+ | |||
+ | The following [[Team:Todai-Tokyo/Protocols/Ligation|Ligations]] were performed using the listed fragments and [[Team:Todai-Tokyo/Protocols/Transformation|Transformed]] into ''E. coli'' competent cells: | ||
+ | |||
+ | *pLacI-RBS-yqiT-dterm | ||
+ | ** pLacI-RBS '''S/P''' ([[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] on 10/1) | ||
+ | ** yqiT-dterm '''E/X''' ([[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] on 10/1) | ||
+ | * pAraC-RBS-yqiT-dterm | ||
+ | ** pAraC-RBS '''S/P''' ([[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] on 9/22) | ||
+ | ** yqiT-dterm '''E/X''' ([[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] on 10/1) | ||
+ | |||
+ | |||
+ | <h2> Infusion + Transformation </h2> | ||
+ | |||
+ | The following constructs were created using [[Team:Todai-Tokyo/Protocols/Infusion|Infusion]] and the listed fragments, then [[Team:Todai-Tokyo/Protocols/Transformation|Transformed]] into ''E. coli'' competent cells: | ||
+ | |||
+ | * pLacI-RBS-yqiT-dterm | ||
+ | ** pLacI-RBS '''S/P''' ([[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] on 10/1) as vector | ||
+ | ** yqiT-dterm ([[Team:Todai-Tokyo/Protocols/Miniprep|Miniprepped]] on 10/1) as insert | ||
+ | |||
+ | using the following primers:<BR> | ||
+ | * '''Inf fwd''': agtgtgtcgatgcagcccatgacacacacacagagatag | ||
+ | * '''Inf rev''': ggggagagatatatagagagacacacacagagatatat | ||
+ | |||
+ | |||
+ | <h2> RE Digest + Gel Purification </h2> | ||
+ | |||
+ | The following were [[Team:Todai-Tokyo/Protocols/Restriction Enzyme Digest|Digested]] using the listed Restriction Enzymes and then [[Team:Todai-Tokyo/Protocols/Gel Purification|Gel Purified]]: | ||
+ | |||
+ | * pLacI ([[Team:Todai-Tokyo/Protocols/Miniprep|Miniprepped]] on 10/1): '''SpeI/PstI''' | ||
+ | * RFP-dterm ([[Team:Todai-Tokyo/Protocols/Miniprep|Miniprepped]] on 10/1): '''XbaI/PstI''' | ||
+ | |||
+ | |||
+ | <h2> Colony PCR </h2> | ||
+ | |||
+ | Colonies from the following plates were used for [[Team:Todai-Tokyo/Protocols/Colony PCR|Colony PCR]] using the listed primers: | ||
+ | |||
+ | * EGFP (Transformed on 9/21): 4 colonies | ||
+ | **'''EGFP rev''': atatgagagcgcgcgcagagagagatg | ||
+ | * Venus (Transformed on 9/21): 4 colonies | ||
+ | **'''Venus fwd''': atatgagagcgcgcgggggagagagagatg |
Latest revision as of 10:14, 20 October 2009
Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook | Protocols | Ethics |
---|
このページの使い方
MiniprepThe following were miniprepped:
PCRThe yqiT gene was PCR amplified from pLacI-yqiT-dterm (miniprepped on 9/7) using the following primers: yqiT fwd: agcccgtgtagtactgtagagtt using PCR program 1 and Ex-taq. Note: This PCR reaction attaches a Biobrick prefix and suffix to the gene. *補足: Program 1と書いてあるところは、いつも使うようなプログラムと違うものを使ってそれを記したい場合はプログラムの内容をリンク先に書き込みましょう。わからない場合は聞いてください。
SequencingThe following were sequenced using the labeled primers:
Results:
TransformationThe following were Transformed into E. coli competent cells:
Ligation + TransformationThe following Ligations were performed using the listed fragments and Transformed into E. coli competent cells:
Infusion + TransformationThe following constructs were created using Infusion and the listed fragments, then Transformed into E. coli competent cells:
using the following primers:
RE Digest + Gel PurificationThe following were Digested using the listed Restriction Enzymes and then Gel Purified:
Colony PCRColonies from the following plates were used for Colony PCR using the listed primers:
|