Team:Groningen/Notebook/Wetwork 25June2012
From 2012.igem.org
Tomvanlente (Talk | contribs) (Created page with "{{headergroningen2012}} Transformation of biobricks BBa_J37034 (LuxI added to GFP) and BBa_R0062 (promotor of LuxR (PR))") |
|||
(4 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
- | {{ | + | {{HeaderGroningen2012}} |
- | Transformation of biobricks BBa_J37034 (LuxI added to GFP) and BBa_R0062 (promotor of LuxR (PR)) | + | <html> |
+ | <head> | ||
+ | <style type="text/css"> | ||
+ | p.margin{ | ||
+ | font-size:12pt; | ||
+ | line-height:14pt; | ||
+ | color:white; | ||
+ | margin-top:0px; | ||
+ | margin-bottom:20px; | ||
+ | margin-left:150px; | ||
+ | margin-right:250px; | ||
+ | } | ||
+ | </style> | ||
+ | </head> | ||
+ | |||
+ | <body> | ||
+ | <p class="margin"><br><br><br><br> | ||
+ | Tom <br> | ||
+ | |||
+ | Transformation of biobricks BBa_J37034 (LuxI added to GFP) and BBa_R0062 (promotor of LuxR (PR)) was succesfull and transferred to LB broth for overnight growth. <br><br> | ||
+ | |||
+ | Nisa and Emeraldo <br> | ||
+ | |||
+ | Preparation for another B. subtilis transformation (BBa_K090403+pigment):<br> | ||
+ | 1.) Preparation of Transformation medium (SMM)<br> | ||
+ | 2.) O/N culture of B. subtilis in SMM<br> | ||
+ | 3.) O/N culture E. coli with BBa_K090403<br> | ||
+ | <br> | ||
+ | Primer design for P alsT with addition of prefix and suffix<br> | ||
+ | 1.) check promoter region (150bp, 250 bp, 300bp, and 500bp before the gene)<br> | ||
+ | 2.) add restriction enzyme sites and 5 bases for plateau of restriction enzymes<br> | ||
+ | 3.) Order the primers<br> | ||
+ | <br> | ||
+ | Preparing starch agar and iodine for checking purpose of B. subtilis transformant <br> | ||
+ | (B. subtilis transformants of BBa_K090403 should not be able to degrade starch)<br> | ||
+ | |||
+ | <br> | ||
+ | <A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A> | ||
+ | </p><br><br> | ||
+ | </body> | ||
+ | </html> | ||
+ | |||
+ | {{Template:SponsorsGroningen2012}} |
Latest revision as of 16:50, 25 September 2012
Tom
Transformation of biobricks BBa_J37034 (LuxI added to GFP) and BBa_R0062 (promotor of LuxR (PR)) was succesfull and transferred to LB broth for overnight growth.
Nisa and Emeraldo
Preparation for another B. subtilis transformation (BBa_K090403+pigment):
1.) Preparation of Transformation medium (SMM)
2.) O/N culture of B. subtilis in SMM
3.) O/N culture E. coli with BBa_K090403
Primer design for P alsT with addition of prefix and suffix
1.) check promoter region (150bp, 250 bp, 300bp, and 500bp before the gene)
2.) add restriction enzyme sites and 5 bases for plateau of restriction enzymes
3.) Order the primers
Preparing starch agar and iodine for checking purpose of B. subtilis transformant
(B. subtilis transformants of BBa_K090403 should not be able to degrade starch)
Back to notebook