Team:Wageningen UR/Journal/week13

From 2012.igem.org

(Difference between revisions)
(Lab work)
 
(9 intermediate revisions not shown)
Line 1: Line 1:
{{Template:WUR}}
{{Template:WUR}}
-
= week 13: 23 july - 27 july =
+
= week 13: 23 july - 29 july =
 +
Not much work was done this week because the team spent four days on going to a three day synthetic biology conference in Munich. We learned a lot there and had a great time!
-
== Office work ==
+
== Lab work ==
 +
''' CCMV '''
 +
 +
''27th July'' (Hugo)
 +
<br/>
 +
Another PCR repeat of 18-07's PCR. Purified PCR products using Fermentas PCR Purification Kit then ran another PCR reaction (repeat of 19-07).
 +
<br/>
 +
<br/>
 +
 +
''28th July'' (Jeroen)
 +
* Digested IPTG inducible promotor with RBS brick: Spe1 and Pst1
 +
* Digested CCMV pJET fragment with Xba1 and Pst1
 +
* after 30 minutes used a PCR purification for digestion inactivation (Pst1 is not heat inactivatable)
 +
* Ligation 1 hour
 +
* Transformation of DH5alpha cells
 +
 +
''30th July'' (Jeroen)
 +
* 5 colonies picked for colony PCR per plate
 +
 +
 +
'''PLRV'''
 +
 +
* RNA isolation of potato leaf tissue
 +
 +
* Reverse transcriptase reaction to obtain cDNA
 +
 +
* PCR on cDNA using coat protein primers
 +
 +
 +
The figure below shows the purity of isolated RNA. We isolated RNA of different potato cultivars.
 +
 +
[[File:rna2.jpg|frame|center|''Figure 1: isolated RNA PLRV'']]
 +
 +
[[File:table1.jpg|frame|center|''Figure 2: ...'']]
 +
 +
 +
We performed Reverse Transciptase reactions followed by PCR. We used the Revert AID H Minus Reverse Transcription Kit (Fermentas).
 +
 +
[[File:rt-pcr.jpg|frame|center|''Figure 3: ...'']]
 +
 +
Agarose gel of PCR products. Lanes 1 till 4 show the PLRV Coat Protein (CP) bands with the expected size of 627 bp. Lanes 6 till 9 show the PLRV Coat Protein plus Read Through part (CP_RT) with the expected size of 2154 bp.
-
== Lab work ==
 
-
RNA isolation of potato leaf tissue
 
-
Reverse transcriptase reaction to obtain cDNA
 
-
PCR on cDNA using coat protein primers
 
-
Written by: Wouter
 
----
----
[[https://2012.igem.org/Team:Wageningen_UR/Journal/week12 previous week]]          [[https://2012.igem.org/Team:Wageningen_UR/Journal/week14 next week]]
[[https://2012.igem.org/Team:Wageningen_UR/Journal/week12 previous week]]          [[https://2012.igem.org/Team:Wageningen_UR/Journal/week14 next week]]

Latest revision as of 03:26, 27 September 2012

week 13: 23 july - 29 july

Not much work was done this week because the team spent four days on going to a three day synthetic biology conference in Munich. We learned a lot there and had a great time!

Lab work

CCMV

27th July (Hugo)
Another PCR repeat of 18-07's PCR. Purified PCR products using Fermentas PCR Purification Kit then ran another PCR reaction (repeat of 19-07).

28th July (Jeroen)

  • Digested IPTG inducible promotor with RBS brick: Spe1 and Pst1
  • Digested CCMV pJET fragment with Xba1 and Pst1
  • after 30 minutes used a PCR purification for digestion inactivation (Pst1 is not heat inactivatable)
  • Ligation 1 hour
  • Transformation of DH5alpha cells

30th July (Jeroen)

  • 5 colonies picked for colony PCR per plate


PLRV

  • RNA isolation of potato leaf tissue
  • Reverse transcriptase reaction to obtain cDNA
  • PCR on cDNA using coat protein primers


The figure below shows the purity of isolated RNA. We isolated RNA of different potato cultivars.

Figure 1: isolated RNA PLRV
Figure 2: ...


We performed Reverse Transciptase reactions followed by PCR. We used the Revert AID H Minus Reverse Transcription Kit (Fermentas).

Figure 3: ...

Agarose gel of PCR products. Lanes 1 till 4 show the PLRV Coat Protein (CP) bands with the expected size of 627 bp. Lanes 6 till 9 show the PLRV Coat Protein plus Read Through part (CP_RT) with the expected size of 2154 bp.





[previous week] [next week]