Team:UNITN-Trento/Notebook/Labposts/07/15
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{ | { | ||
- | "date" : "2013-07- | + | "date" : "2013-07-08", |
- | "author" : " | + | "author" : "emil", |
- | "title" : " | + | "title" : " Purification of Inocula (03/7)", |
- | "content" : "<html> | + | "content" : "<html>I verifyed the status of the last inocula(05/7) that resulted a bit strange.</html>{{:Team:UNITN-Trento/Templates/Styles/Spoiler|Inocula|<html><img src=\"\" width=\"450px\" /></html>}}<html>Unfortunately The day before were inoculate uncorrect plates(03/7) so 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_K823026+BBa_E0840(1:1) 1</td><td>438.8 ng/µl</td></tr><tr><td>BBa_K823026+BBa_E0840(1:1) 2</td><td>400.7 ng/µl</td></tr><tr><td>BBa_K823024+BBa_E0840(1:1) 3</td><td>343.6 ng/µl(the only succesful)</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>Ladder 1kb Fermentas</td><td>1</td></tr><tr><td>BBa_K823026+BBa_E0840(1:1) a</td><td>3</td></tr><tr><td>BBa_K823026+BBa_E0840(1:1) b</td><td>4</td></tr><tr><td>BBa_K823024+BBa_E0840(1:1) </td><td>5</td></tr></table></center></html>}}{{:Team:UNITN-Trento/Templates/Styles/Spoiler|Gel image|<html><img src=\"\" width=\"450px\" /></html>}}<html>As we can see only the third(024) sample shows the insert at the right size of 1000 bp(the lower band), then I did the inocula of the plates of 5/07(1:1,1:2,1:3) and of the old plate that gives right results to amplify 024(1:1).</html>", |
- | "tags" : " | + | "tags" : "K823024-K823026-E0840" |
} | } |
Revision as of 08:24, 3 October 2013
{ "date" : "2013-07-08", "author" : "emil", "title" : " Purification of Inocula (03/7)", "content" : "I verifyed the status of the last inocula(05/7) that resulted a bit strange.
Unfortunately The day before were inoculate uncorrect plates(03/7) so I have purified them following the purification protocol these are the results of the quantification.Quantification
Afterwards I screened 800 ng of the samples following the screening protocol with EcoR1 HF and Pst1, these are the results of the gel:Sample | Quantities |
---|---|
BBa_K823026+BBa_E0840(1:1) 1 | 438.8 ng/µl |
BBa_K823026+BBa_E0840(1:1) 2 | 400.7 ng/µl |
BBa_K823024+BBa_E0840(1:1) 3 | 343.6 ng/µl(the only succesful) |
Gel order
As we can see only the third(024) sample shows the insert at the right size of 1000 bp(the lower band), then I did the inocula of the plates of 5/07(1:1,1:2,1:3) and of the old plate that gives right results to amplify 024(1:1).",
"tags" : "K823024-K823026-E0840"
}
Sample | Well |
---|---|
Ladder 1kb Fermentas | 1 |
BBa_K823026+BBa_E0840(1:1) a | 3 |
BBa_K823026+BBa_E0840(1:1) b | 4 |
BBa_K823024+BBa_E0840(1:1) | 5 |