Team:Johns Hopkins/Notebook

From 2008.igem.org

Revision as of 16:37, 12 July 2008 by Ingrid (Talk | contribs)

Notebook

Contents

Files

iGEM Groups V1.0
iGEM Groups V2.01

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
Tuesday July 15: Lab meeting at 6:30PM with Jessica. Have status reports ready.

Status Reports

GROUP 1: Fluorescent Proteins

 status report by: Ingrid (work done by James)
 Part no.: BBa_K110017
 Part Description: yESapphire RtL
 Part Location (in build a genome lab): In James and Jasper's PCR product Box,
 Stainless Steel 4 degree
 PCR successful?; Yes
 Cloning of PCR product successful: Y/N
 Sequencing of cloned PCR product successful: Not done
 Joining of validated part to adjacent part(s) status: Not done
 Problems to be solved: The PCR of this part yielded a very large product
 Current status of this part:
 status report by: Ingrid (work done by James)
 Part no.: BBa_K110010
 Part Description: yESapphire LtR
 Part Location (in build a genome lab): In James and Jasper's PCR product Box, 
 Stainless Steel 4 degree
 PCR successful?; Yes
 Cloning of PCR product successful: Not done 
 Sequencing of cloned PCR product successful: No
 Joining of validated part to adjacent part(s) status: Not done
 Problems to be solved: The PCR of this part yielded a very large product
 Current status of this part:

GROUP 2: MATa Specific-promoters

 Status report by Allison and Nate
 Part no.: BBa_K110008
 Part Description: MFA1 (L+R)
 Part Location: in a labeled box, second shelf from the top, -20
 degrees C refrigerator next to front door
 Date: 7/10/08
 PCR successful? Yes
 Cloning of PCR product successful: in progress
 Sequencing of cloned PCR product successful: not done
 Joining of validated part to adjacent part(s) status: not done
 Problems to be solved: to be determined
 Current status of this part: PCR was being troubleshooted, appeared to
 have good results with regular PCR protocol (not touchdown) in which
 there was a constant annealing temperature of 55 degrees C - see gel
 Status report by Allison and Nate
 Part no.: BBa_K110016
 Part Description: Ste2 (R+L)
 Part Location: in a labeled box, second shelf from the top, -20
 degrees C refrigerator next to front door
 Date: 7/10/08
 PCR successful? Yes
 Cloning of PCR product successful: in progress
 Sequencing of cloned PCR product successful: not done
 Joining of validated part to adjacent part(s) status: not done
 Problems to be solved: to be determined
 Current status of this part: Both PCR protocols (touchdown and second
 PCR with constant annealing temperature) produced product of the
 correct size. BBa_K110016 was used as a control in the second PCR with
 BBa_K110008.

GROUP 3

GROUP 4

GROUP 5

etc....