Team:KIT-Kyoto/Notebook/growcurves
From 2013.igem.org
Line 30: | Line 30: | ||
<P STYLE="margin-bottom: 0cm"><BR> | <P STYLE="margin-bottom: 0cm"><BR> | ||
</P> | </P> | ||
- | <P STYLE="margin-bottom: 0cm"> | + | <P STYLE="margin-bottom: 0cm">(1)<FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">2012KitPlate2,6O(pSB1A3)</FONT></SPAN></FONT></P> |
- | <P STYLE="margin-bottom: 0cm"> | + | <P STYLE="margin-bottom: 0cm">(2)<FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">2012KitPlate2,8A(pSB1A2)</FONT></SPAN></FONT></P> |
- | <P STYLE="margin-bottom: 0cm"> | + | <P STYLE="margin-bottom: 0cm">(5)<FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">2013KitPlate5,15J(pSB1A2)</FONT></SPAN></FONT></P> |
- | <P STYLE="margin-bottom: 0cm"> | + | <P STYLE="margin-bottom: 0cm">(6)<FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">2013KitPlate5,24E(pSB1A2)</FONT></SPAN></FONT></P> |
<P STYLE="margin-bottom: 0cm"><BR> | <P STYLE="margin-bottom: 0cm"><BR> | ||
</P> | </P> | ||
<P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | <P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | ||
- | obtained colonies of sample | + | obtained colonies of sample (1), (2), and (6), but did not "5".</FONT></SPAN></FONT></P> |
<P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | <P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | ||
- | prepared sample | + | prepared sample (5) again and got it.</FONT></SPAN></FONT></P> |
<P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | <P STYLE="margin-bottom: 0cm"><FONT FACE=""><SPAN LANG="en-US"><FONT SIZE=2 STYLE="font-size: 11pt">We | ||
cultured each transformant in 3 ml LB liquid medium containing | cultured each transformant in 3 ml LB liquid medium containing |
Revision as of 05:10, 27 September 2013
Growth curves
August 20th,21st
We transformed four kinds of plasmid DNA into E.coli cells.
These plasmids were obtained from iGEM DNA distributions kit (listed below).
We added 10ul of water into the samples and left them for 5 minutes before using the parts.
(1)2012KitPlate2,6O(pSB1A3)
(2)2012KitPlate2,8A(pSB1A2)
(5)2013KitPlate5,15J(pSB1A2)
(6)2013KitPlate5,24E(pSB1A2)
We obtained colonies of sample (1), (2), and (6), but did not "5".
We prepared sample (5) again and got it.
We cultured each transformant in 3 ml LB liquid medium containing ampicillin (37°C, 125rpm overnight).
August 23rd~September 3rd
We measured the turbidities of the transformants (OD600).
We transferred the transformant prepared on 8/22 to 200 mL flasks.
We measured the turbidities every 30 minutes.
But we could not get positive data.
The data are indicated below.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
We measured the turbidities of the transformants (OD600).
We transferred the transformant prepared on 8/25 to 200 mL flasks.
We measured the turbidities every 30 minutes.
But we could not get positive data.
The data are indicated below.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
We measured the turbidities of the transformants (OD600).
We transferred the transformant prepared on 8/26 to 200 mL flasks.
We measured the turbidities every 30 minutes.
But we could not get positive data.
The data are indicated below.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
We measured the turbidities of the transformants (OD600).
We transferred the transformant prepared on 9/2 to 200 mL flasks.
We measured the turbidities every 30 minutes.
But we could not get positive data.
The data are indicated below.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
September 4th~7th
We measured the turbidities of the transformants at hourly intervals and made the growth curves.
We transferred the transformant prepared on 9/3 to 200 mL flasks.
We measured the turbidities every 1 hour.
The measurements were carried out for 12 hours.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
37°C, 125rpm
Control:HST08
We measured the turbidities of the transformants at hourly intervals and made the growth curves.
We transferred the transformant prepared on 9/4 to 200 mL flasks.
We measured the turbidities every 1 hour.
The measurements were carried out for 12 hours.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
37°C, 125rpm
Control:HST08
We measured the turbidities of the transformants at hourly intervals and made the growth curves.
We transferred the transformant prepared on 9/5 to 200 mL flasks.
We measured the turbidities every 1 hour.
The measurements were carried out for 12 hours.
Liquid LB |
50mL |
Sample |
20μL |
Ampicillin |
75μL |
37°C, 125rpm
Control:HST08