Team:Hawaii/Notebook/2008-09-13

From 2008.igem.org

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===PCR===
===PCR===
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<strong>Margaret</strong>  
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:<strong>Margaret</strong>  
:*oriT constuct from pSB1A2- for construction with J33207 for verification test
:*oriT constuct from pSB1A2- for construction with J33207 for verification test
:*rep (pRL1383a)- to ligate to plac, B0030, and pSB1A3 and make a number of construct that can be sequenced with my new primers
:*rep (pRL1383a)- to ligate to plac, B0030, and pSB1A3 and make a number of construct that can be sequenced with my new primers
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===Restriction Digest===
===Restriction Digest===
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<strong>Margaret</strong>
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:<strong>Margaret</strong>
:*Code
:*Code
::*a= aadA
::*a= aadA
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::*first #= colony from aada+pSB1A3 ligation (sequence verified)
::*first #= colony from aada+pSB1A3 ligation (sequence verified)
::*second#= colony from plac,B0034 ligation to the sequence verified aadA+pSB1A3 ligation
::*second#= colony from plac,B0034 ligation to the sequence verified aadA+pSB1A3 ligation
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{|class=wikitable border=1  
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{|class=wikitable border=1 align=center
!construct
!construct
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!Re-enzymes used
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!RE-enzymes used
!next step
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|EP
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|ligate to self(use as control)
|ligate to self(use as control)
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== Drylab Work ==
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===Name of Task===
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:<strong> name of person/people who performed the task</strong>
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:* Summary of task and what was done. Link to experiment for detailed notes if necessary.
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:* e.g. read through papers, worked on proposal, etc.
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= Discussion =
= Discussion =

Latest revision as of 08:13, 15 September 2008

Projects Events Resources
Sponsors Experiments Milestones Protocols
Notebook (t) Meetings (t)

Things we did today

Wetlab work

Competent Cells

Margaret, Krystle, Norman
  • Today we made DH5-alpha competent cells. The first OD reading was between 0.3-0.4 for all three flasks. The OD after the last incubation with CMBD buffer was 1.1, 1.29, 0.8977, 1.079, and 0.942. (both of these OD readings are within the range we want.)

PCR

Margaret
  • oriT constuct from pSB1A2- for construction with J33207 for verification test
  • rep (pRL1383a)- to ligate to plac, B0030, and pSB1A3 and make a number of construct that can be sequenced with my new primers
  • omega interposon contruct from pSB1A2- to verify and sequence
  • oriV(pRL1383a)- to ligate to pSB1A3 and sequence next week.
  • (+) control pSB1A3 with VF2&VR
  • (-) control water with VF2&VR

Restriction Digest

Margaret
  • Code
  • a= aadA
  • p=pRL1383a
  • b=from BB registry
  • first #= colony from aada+pSB1A3 ligation (sequence verified)
  • second#= colony from plac,B0034 ligation to the sequence verified aadA+pSB1A3 ligation
construct RE-enzymes used next step
J33207 SP dephosphorylate
ap36 E, S gel purify
ap32 E, S gel purify
ap61 E, S gel purify
ab95 E, S gel purify
ab92 E, S gel purify
ab96 E, S gel purify
ab94 E, S gel purify
ab98 E, S gel purify
ab93 E, S gel purify
base vector(I15020) N dephosphorylate
oriT(BB) XP ligate directly
oriT(my construct)PCR product 9/13 XP ligate directly
TT(B0016) XP ligate directly
pSB1A3 EP ligate to self(use as control)

Discussion

Quote of the Day

History is the only laboratory we have in which to test the consequences of thought. - Étienne Gilson


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