From 2013.igem.org
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| | { | | { |
| - | "date" : "2013-07-09", | + | "date" : "2013-07-23", |
| - | "author" : "emil", | + | "author" : "fabio", |
| - | "title" : " Purification of Inocula (05/7) and re-ligation and re-transformation ", | + | "title" : " the blue ligation: the never ending story !", |
| - | "content" : "<html>Unfortunately only one of the inocula of 05/7 has succeded and shows an incorrect red color(RFP the previous insert) so I decided to purify and quantfy only the 2 attempt to amplify 024.I have purified them following the <a href=\"https://2013.igem.org/Team:UNITN-Trento/Protocols#miniprep\"> purification protocol </a> these are the results of the quantification.</html>{{:Team:UNITN-Trento/Templates/Styles/Spoiler|Quantification|<html><center><table class=\"tn-sp-table\"><tr><th>Sample</th><th>Quantities</th></tr><tr><td>BBa_K823024+BBa_E0840(1:1) 2</td><td>267 ng/µl</td></tr><tr><td>BBa_K823024+BBa_E0840(1:1) 3</td><td>248.6 ng/µl</td></tr></table></center></html>}}<html>Afterwards I screened 800 ng of the samples following the <a href=\"https://2013.igem.org/Team:UNITN-Trento/Protocols#Digestion\"> screening protocol </a> with EcoR1 HF and Pst1, these are the results of the gel:</html>{{:Team:UNITN-Trento/Templates/Styles/Spoiler|Gel order|<html><center><table class=\"tn-sp-table\"><tr><th>Sample</th><th>Well</th></tr><tr><td>BBa_K823024+BBa_E0840(1:1) b</td><td>1</td></tr><tr><td>BBa_K823024+BBa_E0840(1:1) </td><td>2</td></tr><tr><td>Ladder 1kb Fermentas</td><td>3</td></tr></table></html>}}{{:Team:UNITN-Trento/Templates/Styles/Spoiler|Gel image|<html><img src=\"https://static.igem.org/mediawiki/2013/9/94/Tn-20130709-d.jpg\" /></html>}}<html>No one of the sample has succeded there are only the bands of the backbone and ther aren't visible inserts of any kind, so I decided to re-try the ligation with two couples of 026 and GFP(026a=36.3 ng/µl,026b=37.6ng/µl,GFPa=15.9ng/µl,GFPb015.8ng/µl,I have done it following the <a href=\"https://2013.igem.org/Team:UNITN-Trento/Protocols#Ligation\"> ligation protocol </a>(I have only changed the amaunt of plasmid:300 ng).Afterwards I have transformed and plated on ampicillin agar 8 NEB10β (2 ctrl,2 1:1, 2 1:2, 2 1:3).I have also amplified the 024(2 inocula).</html>", | + | "content" : "<html> this morning I added Sap to the 016 digestion and dPnl to the other two, then I purified them and quantified'em: <br>O16: 29,8 ng/ul <br>006: 16,2 ng/ul <br>R0010: 6,1 ng/ul <br>Then I started the ligation following the ligation protocol: at the end of it, I transformed 10ul of the ligation in 200 Neb10b and plated.Meanwhile Bruno miniprepped k952003 inocula and the screening was successful!!</html>", |
| - | "tags" : "K832024-K823026-E0840" | + | "tags" : " YF1_FixJ - FixK2- ho1_PcyA_cph8-OmpR- YF1_FixJ_PfixK2_amilGFP " |
| | } | | } |
Revision as of 08:37, 3 October 2013
{
"date" : "2013-07-23",
"author" : "fabio",
"title" : " the blue ligation: the never ending story !",
"content" : " this morning I added Sap to the 016 digestion and dPnl to the other two, then I purified them and quantified'em:
O16: 29,8 ng/ul
006: 16,2 ng/ul
R0010: 6,1 ng/ul
Then I started the ligation following the ligation protocol: at the end of it, I transformed 10ul of the ligation in 200 Neb10b and plated.Meanwhile Bruno miniprepped k952003 inocula and the screening was successful!!",
"tags" : " YF1_FixJ - FixK2- ho1_PcyA_cph8-OmpR- YF1_FixJ_PfixK2_amilGFP "
}
"
