Team:UNIPV-Pavia/Notebook/Week1

From 2008.igem.org

(Difference between revisions)
Line 32: Line 32:
'''05/19/08'''
'''05/19/08'''
 +
<br>
Let’s start our IGEM 2008 experience!
Let’s start our IGEM 2008 experience!
At first, we broke the punch tool…:)
At first, we broke the punch tool…:)
Line 37: Line 38:
We used a scalpel to cut and resuspend the following 22 paper spots:
We used a scalpel to cut and resuspend the following 22 paper spots:
-
BBa_I14032 BBa_R0079 BBa_R0062 BBa_R0040
+
{|cellpadding="20"
-
BBa_R0082 BBa_R0051 BBa_J23100 BBa_C0161
+
|BBa_I14032
-
BBa_C0062 BBa_C0078 BBa_C0179 BBa_C0051
+
|BBa_R0079
-
BBa_C0012 BBa_C0040 BBa_I15010 BBa_I15008
+
|BBa_R0062
-
BBa_I15009 BBa_E0040 BBa_E1010 BBa_B0030
+
|BBa_R0040
-
BBa_B1006 BBa_E0240
+
|-
-
 
+
|BBa_R0082
 +
|BBa_R0051
 +
|BBa_J23100
 +
|BBa_C0161
 +
|-
 +
|BBa_C0062
 +
|BBa_C0078
 +
|BBa_C0179
 +
|BBa_C0051
 +
|-
 +
|BBa_C0012
 +
|BBa_C0040
 +
|BBa_I15010
 +
|BBa_I15008
 +
|-
 +
|BBa_I15009
 +
|BBa_E0040
 +
|BBa_E1010
 +
|BBa_B0030
 +
|-
 +
|BBa_B1006
 +
|BBa_E0240
 +
|}
We used tweezers to put the cut paper into tubes containing 10 μl of warmed TE buffer.
We used tweezers to put the cut paper into tubes containing 10 μl of warmed TE buffer.

Revision as of 17:35, 27 May 2008


Home.jpg Home Unipv logo.jpg The Team And.jpg The Project Safety.jpg Biological Safety Dna.png Parts Submitted to the Registry
Laptop.jpg Dry Lab Pipette.jpg Wet Lab Math.gif Modeling Note.jpg Protocols Notebook.gif Activity Notebook



Notebook



Week 1 Week 2



Week 1: 05/19/08 - May 05/23/08

05/19/08
Let’s start our IGEM 2008 experience! At first, we broke the punch tool…:)

We used a scalpel to cut and resuspend the following 22 paper spots:

BBa_I14032 BBa_R0079 BBa_R0062 BBa_R0040
BBa_R0082 BBa_R0051 BBa_J23100 BBa_C0161
BBa_C0062 BBa_C0078 BBa_C0179 BBa_C0051
BBa_C0012 BBa_C0040 BBa_I15010 BBa_I15008
BBa_I15009 BBa_E0040 BBa_E1010 BBa_B0030
BBa_B1006 BBa_E0240

We used tweezers to put the cut paper into tubes containing 10 μl of warmed TE buffer.

We transformed 60 µl of TOP10 E. coli with 4 µl of DNA in TE for all 22 parts, plated transformed bacteria and incubated overnight at 37°C.

We used LB medium previously prepared, with the suitable antibiotic added.

Retrieved from "http://2008.igem.org/Team:UNIPV-Pavia/Notebook/Week1"