Team:Johns Hopkins/Notebook

From 2008.igem.org

(Difference between revisions)
(GROUP 1: Fluorescent Proteins)
(GROUP 1: Fluorescent Proteins)
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Date: July 22, 2008
Date: July 22, 2008
Status report by: Tejas
Status report by: Tejas
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  Part no.: BBa_K110017 -> BBa_K110023
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Part no.: BBa_K110017 -> BBa_K110023
-
  Part Description: yESapphire , mCherry, venusYFP, and Citrine
+
Part Description: yESapphire , mCherry, venusYFP, and Citrine
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  Work on yESapphire was gratiously done by James. Primers were designed. Restriction site ends
+
Work on yESapphire was gratiously done by James. Primers were designed. Restriction site ends have been added through PCR. The product was cloned into JM109. Colonies were picked and an inoculation was grown. Miniprep was performed and subsequent DNA was CS PCR'd and run on a gel to verify contents <b>([http://www.jhu.edu/iGEM/Group3:ShortTwo-wayStops/2008-7-22.Short%202Way%20Stop,%20Alpha%20Promoters,%20&%20Sapphire%20FP.Allison%20Suarez%20and%20Nate%20Sotuyo%20.html Short 2Way Stop, Alpha Promoters, & Sapphire FP])</b>. BioBrick is currently being sequenced.
-
  have been added through PCR. The product was cloned into JM109. Colonies were picked and an
+
-
  inoculation was grown. Miniprep was performed and subsequent DNA was CS PCR'd and run on a gel
+
-
  to verify contents <b>([http://www.jhu.edu/iGEM/Group3:ShortTwo-wayStops/2008-7-22.Short%202Way%20Stop,%20Alpha%20Promoters,%20&%20Sapphire%20FP.Allison%20Suarez%20and%20Nate%20Sotuyo%20.html Short 2Way Stop, Alpha Promoters, & Sapphire FP])</b>. BioBrick is currently being
+
-
  sequenced.
+
    
    
-
  Work on mCherry and venusYFP (BBa_K110018 -> BBa_K110021) is currently being done. Primers were
+
Work on mCherry and venusYFP (BBa_K110018 -> BBa_K110021) is currently being done. Primers were designed. Restriction sites have been added through PCR.  
-
  designed. Restriction sites have been added through PCR.  
+
   [http://www.jhu.edu/iGEM/Group1:FluorescentProteins/2008-7-23.PCR%20Products:%20mCherry%20and%20Venus%20YFP,%20both%20RtL%20and%20LtR.Ingrid,%20Tejas.html PCR Products: mCherry and Venus YFP, both RtL and LtR] The products were cloned into JM109 and
   [http://www.jhu.edu/iGEM/Group1:FluorescentProteins/2008-7-23.PCR%20Products:%20mCherry%20and%20Venus%20YFP,%20both%20RtL%20and%20LtR.Ingrid,%20Tejas.html PCR Products: mCherry and Venus YFP, both RtL and LtR] The products were cloned into JM109 and
   plated. 3 colonies per 4 BioBricks (total 12) were picked, grown out, miniprepped, and digested
   plated. 3 colonies per 4 BioBricks (total 12) were picked, grown out, miniprepped, and digested

Revision as of 13:51, 23 July 2008

Contents

Groups

iGEM Groups 1.0
iGEM Groups 2.01
iGEM Groups 2.02

Important reminders and notes

 [Can make general comments here, so they don't get lost in peoples e-mail boxes]
 
 July 11: Primers for group 1 were delivered yesterday.
 July 11: Lab meeting at 7:30PM in the lab to go over miniprep protocol.
 July 15: Lab meeting at 6:30PM with Jessica. Have status reports ready. 
          Bring labtop if you can.
 July 17: Restriction Digest/Sequencing Preparation (with James) 6:00PM.
 July 21: 6:00PM or 6:30PM Lab meeting with Jessica. Have status reports ready.

Data

To upload data, go here, click on upload data, and provide the necessary information and results.

Status Reports

The status reports of each group below will continuously be updated as we work on the biobricks. The following PDFs contain progressive versions of our status reports as we continue through the sex detector project; they are added weekly. To learn more about each biobrick, please refer to the Biobrick page.

Status Report 2.1 - 07/12/08
Status Report 2.2 - 07/17/08

Please BOLD the most recent step that you have completed. Do this by placing the tag < b > in front of and </ b > at the end of what you would like to be placed in bold (with no space between letter and carrot symbol (<,>).

GROUP 1: Fluorescent Proteins

Summary for Fluorescent Proteins Group

Date: July 22, 2008
Status report by: Tejas
Part no.: BBa_K110017 -> BBa_K110023
Part Description: yESapphire , mCherry, venusYFP, and Citrine

Work on yESapphire was gratiously done by James. Primers were designed. Restriction site ends have been added through PCR. The product was cloned into JM109. Colonies were picked and an inoculation was grown. Miniprep was performed and subsequent DNA was CS PCR'd and run on a gel to verify contents <b>([http://www.jhu.edu/iGEM/Group3:ShortTwo-wayStops/2008-7-22.Short%202Way%20Stop,%20Alpha%20Promoters,%20&%20Sapphire%20FP.Allison%20Suarez%20and%20Nate%20Sotuyo%20.html Short 2Way Stop, Alpha Promoters, & Sapphire FP])</b>. BioBrick is currently being sequenced.
  
Work on mCherry and venusYFP (BBa_K110018 -> BBa_K110021) is currently being done. Primers were designed. Restriction sites have been added through PCR. 
  [http://www.jhu.edu/iGEM/Group1:FluorescentProteins/2008-7-23.PCR%20Products:%20mCherry%20and%20Venus%20YFP,%20both%20RtL%20and%20LtR.Ingrid,%20Tejas.html PCR Products: mCherry and Venus YFP, both RtL and LtR] The products were cloned into JM109 and
  plated. 3 colonies per 4 BioBricks (total 12) were picked, grown out, miniprepped, and digested
  for verification on a gel.
   According to the results, (<b>[http://www.jhu.edu/iGEM/Group1:FluorescentProteins/2008-7-22.Venus%20YFP%20and%20mCherry%20Miniprep%20check%20via%20digest.Ingrid.html Venus YFP and mCherry Miniprep check via digest]</b>), only one of the
  mCherry's (BBa_K110019) is the correct product. This product will be retransformed to yield more
  for sequencing. New colonies for the other three BioBricks were selected by Ingrid on 7.22.2008 and
  are being grown out. Process will continue as per protocol.
  
   Work on Citrine has not yet begun. Primers have been designed and ordered, but template DNA must
  be grown out. Template DNA will be grown and extracted by James should we later decide that Citrine
  will be needed.
  
  *Note that mCherry and Citrine both have restriction sites within the coding region, and are
  therefore not optimal. Advice/help on this issue would be appreciated.  

GROUP 2: MATa Specific-promoters

Summary for MATa Specific Promoters Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.

GROUP 3: Short Two-Way Stops

Summary for Short Two-Way Stops Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.

GROUP 4: Long Two-Way Stops & MAT(alpha) Specific Promotors

Summary for Long Two-Way Stops & MAT(alpha) Specific Promoters Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.

GROUP 5: MATa Specific Promoters II

Summary for MATa Specific Promoters II Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.

GROUP 6: Vectors

Summary for Vectors Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.

GROUP 7: Microscopy/Yeast

Summary for Microscopy/Yeast Group

 Date: _________ __, 2008
 Status report by: _____
 Part no.: BBa_K1100XX -> BBa_K1100YY
 Part Description:
 
 Summary here.