Team:Hawaii/Notebook/2008-09-13
From 2008.igem.org
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+ | ::*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 | ||
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== Drylab Work == | == Drylab Work == | ||
Revision as of 07:11, 14 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) |