Team:Heidelberg/Templates/DelH week5

From 2013.igem.org

(Difference between revisions)
 
(One intermediate revision not shown)
Line 21: Line 21:
<br/>
<br/>
[[File:Heidelberg_20130528 2log 2xpSB6A1.png|200px|thumb|right|'''Fig.5.1''' Generation of pSB6A1 for Backbone generation (loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l2-3:''digested pSB6A1 <br/> expected band at 4 Kb was cut out]]
[[File:Heidelberg_20130528 2log 2xpSB6A1.png|200px|thumb|right|'''Fig.5.1''' Generation of pSB6A1 for Backbone generation (loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l2-3:''digested pSB6A1 <br/> expected band at 4 Kb was cut out]]
-
<div style="clear:both"></div>
 
:=> Expected bands are present. Backbone pSB6A1 was cut out and gel purified (c=4 ng/µl).
:=> Expected bands are present. Backbone pSB6A1 was cut out and gel purified (c=4 ng/µl).
 +
<div style="clear:both"></div>
===Generation of AraC Fragment===
===Generation of AraC Fragment===
====Gel Extraction====  
====Gel Extraction====  
Line 75: Line 75:
====Result====  
====Result====  
2 of the colonies turned blue
2 of the colonies turned blue
-
:=> Perform miniprep.
+
:=> Perform [https://2013.igem.org/Team:Heidelberg/Project/Methods miniprep].
 +
 
====Miniprep====
====Miniprep====
Miniprep was performed according to Qiagen's instructions.
Miniprep was performed according to Qiagen's instructions.
Line 129: Line 130:
<br/>
<br/>
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
-
<div style="clear:both"></div>
+
 
The gel shows a lot unspecific bands for both DelH F1a samples.
The gel shows a lot unspecific bands for both DelH F1a samples.
:=> Fragment was cut and gel purified.
:=> Fragment was cut and gel purified.
<br/>
<br/>
-
 
+
<div style="clear:both"></div>
=== DelH F1b===
=== DelH F1b===
====PCR Conditions F1b.W5.A====
====PCR Conditions F1b.W5.A====
Line 175: Line 176:
<br/>
<br/>
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
-
<div style="clear:both"></div>
+
 
Gel shows one band at the expected length of 5 Kb, but also other side bands below and a huge, bright band at 2 Kb.
Gel shows one band at the expected length of 5 Kb, but also other side bands below and a huge, bright band at 2 Kb.
:=> Band was cut and gel isolated.
:=> Band was cut and gel isolated.
<br/>
<br/>
 +
<div style="clear:both"></div>
=== DelH F2===
=== DelH F2===
====PCR Conditions F2.W5.A====
====PCR Conditions F2.W5.A====
Line 220: Line 222:
<br/>
<br/>
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
[[File:Heidelberg_20130527 2log 1a 1b 2log 2.png|200px|thumb|right|'''Fig.5.2''' PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR) <br> ''l1:''2-log ladder, ''l3-4:''F1a,''l5-6:''F1b,''l7-8:''F2 ]]
-
<div style="clear:both"></div>
+
 
There was a specific band at 8 Kb.
There was a specific band at 8 Kb.
:=> Fragment was cut and gel extracted.
:=> Fragment was cut and gel extracted.
<br/>
<br/>
 +
<div style="clear:both"></div>

Latest revision as of 18:47, 23 October 2013

Contents

27-05 - 02-06-13

Generation of pSB6A1

Miniprep

  • Grow pSB6A1 from glycerol stock in 2 ml LB Amp ON at 37°C.
  • Miniprep using miniprep kit from Qiagen and dilute in 30 µl ddH2O.

Result

Concentration 69.5 ng/µl

Digest

  • The pSB6A1 was generated from the parts registry and cut with EcoRI & PstI
Template DNA BSA NEBuffer2 Enzymes ddH2O Total amount
15 µl (69.5 ng/µl) 5 µl 5 µl 2x 1.5 µl EcoRI-HF & PstI 22 µl 50 µl
The digest was incubated 45 min at 37°C.

Result

Expected band: 3985 bp (pSB6A1) and at 1106 bp (insert=J04450)

Fig.5.1 Generation of pSB6A1 for Backbone generation (loaded 50 µL of PCR)
l1:2-log ladder, l2-3:digested pSB6A1
expected band at 4 Kb was cut out
=> Expected bands are present. Backbone pSB6A1 was cut out and gel purified (c=4 ng/µl).

Generation of AraC Fragment

Gel Extraction

Gel extraction was performed with the gel extraction kit from Qiagen of gel slice (cut 24-05) and was eluted in 30 µl.

Result

The measured concentrations are shown in the table below and was stored at -20°C.

Sample Concentration [ng/µl]
AraC 22.5

Generation of lacZ Fragment

Gel Extraction

Gel extraction was performed with the gel extraction kit from Qiagen of gel slice (cut 24-05) and was eluted in 30 µl.

Result

The measured concentrations are shown in the table below and was stored at -20°C.

Sample Concentration [ng/µl]
lacZ 42.5

Generation of Backbone pSB6A1-AraC-lacZ

Ligation of pSB6A1 with AraC-lacZ

A ligation was performed of fragments for 1 h at RT.

Sample Concentration [ng/µl] Amount for ligation [µl]
pSB6A1 4 12.5
AraC-lacZ 22.5 3.5
T4-ligase - 1
Buffer - 2
ddH2O - 1
Final volume - 20
  • The ligase was inactivated by heat shock for 5 min at 70°C.

Transformation

  • Afterwards, a transformation was performed with 15 µl of the ligation reaction in competent TOP10.
  • Cells were streaked on LB Amp plates and incubated ON at 37°C.

Induction

  • The following day, 5 white colonies were picked (because the red ones still have the mRFP insert J04450) and were incubated in 2 ml LB Amp with 20 µl Arabinose (10%) and 100 µl X-Gal (20 ng/µl).

Result

2 of the colonies turned blue

=> Perform miniprep.

Miniprep

Miniprep was performed according to Qiagen's instructions.

Result

Sample Concentration [ng/µl]
pSB6A1-AraC-lacZ 99


DelH F1a

PCR Conditions F1a.W5.A

Reagent DelH F1a DelH F1a
Expected length [Kb] 5 5
Template 1 µl D. acidovorans 1 µl D. acidovorans
Primer fw 10 µM DN01 DN01
Primer rev 10 µM DN08 DN08
Phusion Master Mix (2x) 25 µl 25 µl
DMSO 2.5 µl -
ddH2O 20,5 23 µl
Cycles Temperature [°C] Time [s]
1 98 10
16 98 1
62 5
72 2:00 min
1 72 2:30 min
1 4 inf

Result

Expected band: 5 Kb

Fig.5.2 PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR)
l1:2-log ladder, l3-4:F1a,l5-6:F1b,l7-8:F2

The gel shows a lot unspecific bands for both DelH F1a samples.

=> Fragment was cut and gel purified.


DelH F1b

PCR Conditions F1b.W5.A

Reagent DelH F1b
Expected length [Kb] 5
Template 1 µl D. acidovorans
Primer fw 10 µM DN07
Primer rev 10 µM DN02
Phusion Master Mix (2x) 25 µl
DMSO -
ddH2O 23 µl
Cycles Temperature [°C] Time [s]
1 98 10
16 98 1
68 5
72 2:00 min
1 72 2:30 min
1 4 inf

Result

Expected band: 5 Kb

Fig.5.2 PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR)
l1:2-log ladder, l3-4:F1a,l5-6:F1b,l7-8:F2

Gel shows one band at the expected length of 5 Kb, but also other side bands below and a huge, bright band at 2 Kb.

=> Band was cut and gel isolated.


DelH F2

PCR Conditions F2.W5.A

Reagent DelH F2
Expected length [Kb] 8
Template 1 µl glycerol stock
Primer 10 µM fw 0.5 µl DelH_f2_SalI_fw
Primer 10 µM rev 0.5 µl DelH_f2_KpnI_rev
Phusion Master Mix (2x) 25 µl
DMSO 0 µl
ddH2O 23 µl
Cycles Temperature [°C] Time [s]
1 98 10
30 98 1
66 5
72 2:45 min
1 72 2:45 min
1 4 inf

Result

Expected length: 8 Kb

Fig.5.2 PCR of DelH fragment F1a, F1b & F2(loaded 50 µL of PCR)
l1:2-log ladder, l3-4:F1a,l5-6:F1b,l7-8:F2

There was a specific band at 8 Kb.

=> Fragment was cut and gel extracted.