Glasgow/Wetlab/Week9

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!align=center|[https://2007.igem.org/Glasgow https://static.igem.org/mediawiki/2007/thumb/c/cc/Uog.jpg/50px-Uog.jpg] ||  [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#99CCFF size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]]
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!align=center|[[Image:Uog.jpg]] ||  [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]] ||  [[Glasgow/Modeling|<font face=georgia color=#3366CC size=4>Go To <br> Glasgow's <br>Drylab Log</font>]]
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|[https://2007.igem.org/Glasgow/Wetlab/Protocols <font face=georgia color=#99CCFF size=5><b>Protocols</b></font>]
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|[https://2007.igem.org/Glasgow/Wetlab/Protocols <font face=georgia color=#3366CC size=5><b>Protocols</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/References <font face=georgia color=#3366CC size=5><b>References</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/References <font face=georgia color=#3366CC size=5><b>References</b></font>]
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|[https://2007.igem.org/Glasgow/Wetlab/Resources <font face=georgia color=#99CCFF size=5><b>Resources</b></font>]
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|[https://2007.igem.org/Glasgow/Wetlab/Resources <font face=georgia color=#3366CC size=5><b>Resources</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/Orders <font face=georgia color=#3366CC size=5><b>Orders</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/Orders <font face=georgia color=#3366CC size=5><b>Orders</b></font>]
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|[https://2007.igem.org/Glasgow/Wetlab/Biobricks <font face=georgia color=#99CCFF size=5><b>Biobricks<br>Used</b></font>]
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|[https://2007.igem.org/Glasgow/Wetlab/Biobricks <font face=georgia color=#3366CC size=5><b>Biobricks<br>Used</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/Gels <font face=georgia color=#3366CC size=5><b>Gels</b></font>]
|[https://2007.igem.org/Glasgow/Wetlab/Gels <font face=georgia color=#3366CC size=5><b>Gels</b></font>]
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<li>
<li>
-
[[User:Christinemerrick|Christine]] digested minipreps of interest B, C and D suspected to contain (*d→g*) from 24/08/07 with PstI. Miniprep of colony D shows bands of expeceted sizes 1155bp, 549bp, ~1962bp, and 3682bp.
+
[[User:Christinemerrick|Christine]] digested minipreps of interest B, C and D suspected to contain phzD→phzG from 24/08/07 with PstI. Miniprep of colony D shows bands of expeceted sizes 1155bp, 549bp, ~1962bp, and 3682bp.
<li>
<li>
-
Overnights were also set up of colonies K, L, M, N, Q, S and T, each suspected of containing (*a→d*), from plate 2.
+
Overnights were also set up of colonies K, L, M, N, Q, S and T, each suspected of containing phzA→phzD, from plate 2.
</ol>
</ol>
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[[User:christinemerrick|Christine]], [[User:L.McLeay|Lynsey]] and [[User:Mojs|Maia]] did minipreps of overnights of colonies H, I, J, K, L, M, N, O, P, Q, R, S, T, U and V from Plate 2.  [[User:christinemerrick|Christine]] then ran a gel of the minipreps and K, L, M, N, Q, S and T showed bands of interest of ~6.7kb.
[[User:christinemerrick|Christine]], [[User:L.McLeay|Lynsey]] and [[User:Mojs|Maia]] did minipreps of overnights of colonies H, I, J, K, L, M, N, O, P, Q, R, S, T, U and V from Plate 2.  [[User:christinemerrick|Christine]] then ran a gel of the minipreps and K, L, M, N, Q, S and T showed bands of interest of ~6.7kb.
<li>
<li>
-
[[User:christinemerrick|Christine]] digested all minipreps of interest for (*a→d*) and miniprep D of (*d→g*) with EcoRI.  However, none showed bands of interest - possibly a fault of the enzyme, new EcoRI ordered.
+
[[User:christinemerrick|Christine]] digested all minipreps of interest for phzA→phzD and miniprep D of phzD→phzG with EcoRI.  However, none showed bands of interest - possibly a fault of the enzyme, new EcoRI ordered.
{| border="1" cellspacing="0" cellpadding="5" align="center"
{| border="1" cellspacing="0" cellpadding="5" align="center"
|-
|-
|'''Insert'''
|'''Insert'''
-
|(*a→d*)
+
|phzA→phzD
-
|(*d→g*)
+
|phzD→phzG
|-
|-
|'''Enzyme'''
|'''Enzyme'''
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[[User:Christinemerrick|Christine]] digested minipreps of colonies K, L, M, N, Q, S and T, thought to contain (*a→d*) with PstI.  Colonies Q and S showed bands of interest of ~4757bp, ~274bp, and ~1796bp.
[[User:Christinemerrick|Christine]] digested minipreps of colonies K, L, M, N, Q, S and T, thought to contain (*a→d*) with PstI.  Colonies Q and S showed bands of interest of ~4757bp, ~274bp, and ~1796bp.
<li>
<li>
-
[[User:Christinemerrick|Christine]] set up PCR to test for inserts (*a→d*) and (*d→g*) in TOPO vector. Done with Reddymix and Touch2.
+
[[User:Christinemerrick|Christine]] set up PCR to test for inserts phzA→phzD and phzD→phzG in TOPO vector. Done with Reddymix and Touch2.
{| border="1" cellspacing="0" cellpadding="5" align="center"
{| border="1" cellspacing="0" cellpadding="5" align="center"
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|-
|-
|M13 for + *f for
|M13 for + *f for
-
|(*d→g*)
+
|phzD→phzG
|D
|D
|M. prep + Colony
|M. prep + Colony
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|-
|-
|M13 rev + *f for
|M13 rev + *f for
-
|(*d→g*)
+
|phzD→phzG
|D
|D
|M. prep + Colony
|M. prep + Colony
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|-
|-
|M13 for + *b rev
|M13 for + *b rev
-
|(*a→d*)
+
|phzA→phzD
|K, L, M, N, Q, S, T
|K, L, M, N, Q, S, T
|M. prep + Colony
|M. prep + Colony
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|-
|-
|M13 rev + *b rev
|M13 rev + *b rev
-
|(*a→d*)
+
|phzA→phzD
|K, L, M, N, Q, S, T
|K, L, M, N, Q, S, T
|M. prep + Colony
|M. prep + Colony
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<li>
<li>
-
[[User:Christinemerrick|Christine]] digested TOPO thought to contain (*a→d*) and (*d→g*) with SphI.
+
[[User:Christinemerrick|Christine]] digested TOPO thought to contain phzA→phzD and phzD→phzG with SphI.
{| border="1" cellspacing="0" cellpadding="5" align="center"
{| border="1" cellspacing="0" cellpadding="5" align="center"
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|-
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!Result
!Result
|-
|-
-
|(*a→d*)
+
|phzA→phzD
|K, L, M, N, Q, S, T
|K, L, M, N, Q, S, T
|SphI
|SphI
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|
|
|-
|-
-
|(*d→g*)
+
|phzD→phzG
|D
|D
|SphI
|SphI
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<li>
<li>
-
Items sent off for sequencing: (*a→d*) colonies Q and S, (*d→g*) colony D.
+
Items sent off for sequencing: phzA→phzD colonies Q and S, phzD→phzG colony D.
-
 
+
-
</ol>
+
=== Thursday 30th August 2007 ===
=== Thursday 30th August 2007 ===
<ol>
<ol>
<li>
<li>
-
[[User:Christinemerrick|Christine]] began site directed mutagenesis of (*a→d*)Q and S, and (*d→g*) D by setting up the following PCR with KOD and SDM_KOD Program with extension time of 7 min 30 secs.
+
[[User:Christinemerrick|Christine]] began site directed mutagenesis of phzA→phzD Q and S, and phzD→phzG D by setting up the following PCR with KOD and SDM_KOD Program with extension time of 7 min 30 secs.
 +
Labelled as follows:  <br>
 +
'''This table is incorrect, see 04/09/07.'''
{| border="1" cellspacing="0" cellpadding="5" align="center"
{| border="1" cellspacing="0" cellpadding="5" align="center"
-
!Gene
 
-
!Colony
 
-
!Primer Pair
 
|-
|-
-
|(*d→g*)
+
!PCR tube
 +
!Colony DNA is taken from
 +
!Insert
 +
!Primers used
 +
|-
 +
|1A
|D
|D
-
|EcoRI *b for + EcoRI *b rev
+
|phzA→phzD
 +
|EcoRI *B for + EcoRI *B rev
|-
|-
-
|(*d→g*)
+
|1B
|D
|D
-
|PstI *c for + PstI *c rev
+
|phzA→phzD
 +
|PstI *C for + PstI *C rev
|-
|-
-
|(*a→d*)
+
|1C
|S
|S
-
|EcoRI *e for + EcoRI *e rev
+
|phzD→phzG
 +
|EcoRI *E for + EcoRI *E rev
|-
|-
-
|(*a→d*)
+
|1D
|S
|S
-
|PstI *e for + PstI *e rev
+
|phzD→phzG
 +
|PstI *E for + PstI *E rev
|-
|-
-
|(*a→d*)
+
|1E
|S
|S
-
|PstI *f for + PstI *f rev
+
|phzD→phzG
 +
|PstI *F for + PstI *F rev
|-
|-
-
|(*a→d*)
+
|1F
|Q
|Q
-
|EcoRI *e for + EcoRI *e rev
+
|phzD→phzG
 +
|EcoRI *E for + EcoRI *E rev
|-
|-
-
|(*a→d*)
+
|1G
|Q
|Q
-
|PstI *e for + PstI *e rev
+
|phzD→phzG
 +
|PstI *E for + PstI *E rev
|-
|-
-
|(*a→d*)
+
|1H
|Q
|Q
-
|PstI *f for + PstI *f rev
+
|phzD→phzG
 +
|PstI *F for + PstI *F rev
|}
|}
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=== Friday 31st August 2007 ===
=== Friday 31st August 2007 ===
-
----
 
<ol>
<ol>
<li>
<li>
-
[[User:Christinemerrick|Christine]] began site directed mutagenesis of TOPO containing (*a→d*) and (*d→g*) by digesting PCR of colonies D, Q and S (see 30/08/07) with DpnI (see Protocol), and transforming them into TOP10 cells and plating them on carbenicillin plates.
+
[[User:Christinemerrick|Christine]] began site directed mutagenesis of TOPO containing phzA→phzD and phzD→phzG by digesting PCR of colonies D, Q and S (see 30/08/07) with DpnI (see Protocol), and transforming them into TOP10 cells and plating them on carbenicillin plates.
-
</ol>
+
 +
 +
</ol>
 +
<br>
 +
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|-
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![[Glasgow/Wetlab/Week8|<font face=georgia color=#3366CC size=4>Previous  <br>  Week</font>]] || [[Glasgow/Wetlab/Week10|<font face=georgia color=#3366CC size=4>Next <br>  Week</font>]]
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|-
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{| valign=top cellpadding=3
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!align=center|[https://2007.igem.org/Glasgow https://static.igem.org/mediawiki/2007/thumb/c/cc/Uog.jpg/50px-Uog.jpg] ||  [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#99CCFF size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]]
+
!align=center|[[Image:Uog.jpg]] ||  [[Glasgow|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Main Page</font>]] || [[Glasgow/Wetlab|<font face=georgia color=#3366CC size=4>Back To <br> Glasgow's <br> Wetlab Log</font>]]
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Latest revision as of 12:34, 25 October 2007

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Protocols References Resources Orders Biobricks
Used 		Gels

Contents

Week 9

Monday 27th August 2007

  1. Maija performed a PvuI digest for pDntA+3/20G and pDntA+4/6B constructs with Roche's PvuI enzyme. The bands were weird sizes, see the gel here.
    Insert Vector Enzyme Expected size Result
    pDntA 3/20G PvuI 1450bp + 749bp ~2500bp
    pDntA 4/6B PvuI 2375bp + 681bp ~3800bp + ~1250bp
  2. Christine digested minipreps of interest B, C and D suspected to contain phzD→phzG from 24/08/07 with PstI. Miniprep of colony D shows bands of expeceted sizes 1155bp, 549bp, ~1962bp, and 3682bp.
  3. Overnights were also set up of colonies K, L, M, N, Q, S and T, each suspected of containing phzA→phzD, from plate 2.

Tuesday 28 August 2007

  1. Christine, Lynsey and Maia did minipreps of overnights of colonies H, I, J, K, L, M, N, O, P, Q, R, S, T, U and V from Plate 2. Christine then ran a gel of the minipreps and K, L, M, N, Q, S and T showed bands of interest of ~6.7kb.
  2. Christine digested all minipreps of interest for phzA→phzD and miniprep D of phzD→phzG with EcoRI. However, none showed bands of interest - possibly a fault of the enzyme, new EcoRI ordered.
    Insert phzA→phzD phzD→phzG
    Enzyme EcoRI EcoRI
    Fragments If 5'-3' 928bp, 2227bp, 18bp, 3654bp 2997bp, 18bp, 3654bp, 679bp
    Fragments If 3'-5' 928bp, 5597bp, 18bp, 284bp 679bp, 284bp, 18bp, 7046bp

Wednesday 29th August 2007

  1. Scott did colony PCR (see protocol 9) on the assembly transformations carried out yesterday using primers VF2 and VR. Unfortunately it looks as though the combined product is larger than the sum of its parts...
  2. Scott also did the following restriction digests (see Protocol 7):
    Insert Digest 1 (EcoRI/PvuI) Insert Digest 2 (EcoRI/SpeI)
    (Done overnight at 16°C)
    J23119 (tube 1) J61101
    J23119 (tube 2) "


    Destination (EcoRI/XbaI)
    (Done overnight at 16°C)
    J61101
  3. Christine digested minipreps of colonies K, L, M, N, Q, S and T, thought to contain (*a→d*) with PstI. Colonies Q and S showed bands of interest of ~4757bp, ~274bp, and ~1796bp.
  4. Christine set up PCR to test for inserts phzA→phzD and phzD→phzG in TOPO vector. Done with Reddymix and Touch2.
    Primer Combination Gene of Interest Colonies Templates Tested Result
    M13 for + *f for phzD→phzG D M. prep + Colony Non-conclusive
    M13 rev + *f for phzD→phzG D M. prep + Colony Non-conclusive
    M13 for + *b rev phzA→phzD K, L, M, N, Q, S, T M. prep + Colony Non-conclusive
    M13 rev + *b rev phzA→phzD K, L, M, N, Q, S, T M. prep + Colony Non-conclusive
  5. Christine digested TOPO thought to contain phzA→phzD and phzD→phzG with SphI.
    Insert Colony Enzyme Fragments If 5'-3' Fragments If 3'-5' Result
    phzA→phzD K, L, M, N, Q, S, T SphI 2025bp, 4803bp 2595bp, 4232bp
    phzD→phzG D SphI 2843bp, 249bp, 4256bp 3686bp, 3413bp, 249bp
  6. Items sent off for sequencing: phzA→phzD colonies Q and S, phzD→phzG colony D.

    Thursday 30th August 2007

    1. Christine began site directed mutagenesis of phzA→phzD Q and S, and phzD→phzG D by setting up the following PCR with KOD and SDM_KOD Program with extension time of 7 min 30 secs. Labelled as follows:
      This table is incorrect, see 04/09/07.
      PCR tube Colony DNA is taken from Insert Primers used
      1A D phzA→phzD EcoRI *B for + EcoRI *B rev
      1B D phzA→phzD PstI *C for + PstI *C rev
      1C S phzD→phzG EcoRI *E for + EcoRI *E rev
      1D S phzD→phzG PstI *E for + PstI *E rev
      1E S phzD→phzG PstI *F for + PstI *F rev
      1F Q phzD→phzG EcoRI *E for + EcoRI *E rev
      1G Q phzD→phzG PstI *E for + PstI *E rev
      1H Q phzD→phzG PstI *F for + PstI *F rev

    Friday 31st August 2007

    1. Christine began site directed mutagenesis of TOPO containing phzA→phzD and phzD→phzG by digesting PCR of colonies D, Q and S (see 30/08/07) with DpnI (see Protocol), and transforming them into TOP10 cells and plating them on carbenicillin plates.


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