Difference between revisions of "User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2013/01/12"

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|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">PcTF Subcloning in E. coli</span>
 
|style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;">PcTF Subcloning in E. coli</span>
|style="background-color: #F2F2F2" align="center"|<html><img src="/images/9/94/Report.png" border="0" /></html> [[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|<html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>[[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]<html>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]]<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>}}
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|style="background-color: #F2F2F2" align="center"|[[File:Report.png|frameless|link={{#sub:{{FULLPAGENAME}}|0|-11}}]][[{{#sub:{{FULLPAGENAME}}|0|-11}}|Main project page]]<br />{{#if:{{#lnpreventry:{{FULLPAGENAME}}}}|[[File:Resultset_previous.png|frameless|link={{#lnpreventry:{{FULLPAGENAME}}}}]][[{{#lnpreventry:{{FULLPAGENAME}}}}{{!}}Previous entry]]&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;}}{{#if:{{#lnnextentry:{{FULLPAGENAME}}}}|[[{{#lnnextentry:{{FULLPAGENAME}}}}{{!}}Next entry]][[File:Resultset_next.png|frameless|link={{#lnnextentry:{{FULLPAGENAME}}}}]]}}
 
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=01/12/2013=
 
=01/12/2013=
 
Ligation of KAH111, KAH112 and C-His vector in DH5α-T and BL21
 
Ligation of KAH111, KAH112 and C-His vector in DH5α-T and BL21
* The 4 μL of C-His Vector from stock is diluted with 20 μL of nuclease free water, then cut with E/P and purified from the gel.   
+
* The 4 μL of C-His Vector from stock is diluted with 16 μL of nuclease free water, then cut with E/P and purified from the gel.   
 
* Ligations
 
* Ligations
 
{| {{table}} cellspacing="3" <!-- Ligations table -->
 
{| {{table}} cellspacing="3" <!-- Ligations table -->
 
|- bgcolor=#cfcfcf
 
|- bgcolor=#cfcfcf
| Ligation || <font color="blue"><u>Plate results (lig : neg crtl)</u> 12/12/12</font>
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| Ligation || <font color="blue"><u></font>
 
|-
 
|-
| 1. E. coli DH5α-T KAH111(E/P)/size, 20 ng + C-His(E/P)/3600, 26ng || <font color="blue">KAH111/C-His 3:1 No Colonies</font>  
+
| 1. E. coli BL-21 KAH111(E/P)/size, 20 ng + C-His(E/P)/3600, 26ng || <font color="blue">KAH111/C-His 3:1 No Colonies</font>  
 
|-
 
|-
| 2. E. coli BL-21  KAH111(E/P)/size, 16 ng + C-His(E/P)/3600, 25ng || <font color="blue">KAH111/C-His 3:1 No Colonies</font>  
+
| 2. E. coli DH5α-KAH111(E/P)/size, 16 ng + C-His(E/P)/3600, 26ng || <font color="blue">KAH111/C-His 3:1 No Colonies</font>  
 
|-
 
|-
| 3. C-His(E/P)/ 25 ng ||  
+
| 3. E. coli BL-21 KAH112(E/P)/size, 22.8 ng + C-His(E/P)/3600, 26ng || <font color="blue">KAH112/C-His 3:1 No Colonies</font>
 +
|-
 +
| 4. E. coli DH5α-T  KAH111(E/P)/size, 20 ng + C-His(E/P)/3600, 26ng || <font color="blue">KAH112/C-His 3:1 No Colonies</font>
 +
|-
 +
| 5. C-His(E/P)/ 26 ng (Control Plate)||  
 
|}
 
|}
  
 +
* Calculations are for the ng of insert we need to get a 3:1 ratio of insert molecules to 50 ng vector molecules
 
{| {{table}} cellspacing="3" <!-- Ligation rxn table -->
 
{| {{table}} cellspacing="3" <!-- Ligation rxn table -->
| &nbsp;            || 1    || 2  || 3   
+
| &nbsp;            || 1    || 2  || 3  || 4 || 5
 
|-
 
|-
| Insert DNA        || 3.12 || 3.12 || ---
+
| Insert DNA        || 2.34 || 2.34 || 2.05 || 2.05 || ---
 
|-
 
|-
| Vector DNA        || 2.94 || 2.94 || 2.94  
+
| Vector DNA        || 1.92 || 1.92 || 1.92 || 1.92 || 1.92
 
|-
 
|-
| 2x lgn buf (Roche) || 7.06 || 7.06 || 5.0  
+
| 2x lgn buf (Roche) || 5.26 || 5.26 || 5.0 || 5.0 || 5.0
 
|-
 
|-
| T4 ligase (NEB)    || 1.0  || 1.0  || 1.0
+
| T4 ligase (NEB)    || 1.0  || 1.0  || 1.0 || 1.0 || 1.0
 
|-
 
|-
| dH<sub>2</sub>O    || 0 || 0 || 0.88  
+
| dH<sub>2</sub>O    || 0 || 0 || 0.03 || 0.03 || 2.08
 
|-
 
|-
| &nbsp;            || 14.12 μL || 14.12 μL || 10μl
+
| &nbsp;            || 10.52 μL || 10.52 μL || 10μl || 10μL || 10μL
 
|}
 
|}
 +
 +
* The incubation time for the ligation process was 30min at room temperature.
 +
* Fast transformation, 30 min on ice.

Latest revision as of 22:21, 26 September 2017

Owwnotebook icon.pngPcTF Subcloning in E. coli Report.pngMain project page
Resultset previous.pngPrevious entry      Next entryResultset next.png

01/12/2013

Ligation of KAH111, KAH112 and C-His vector in DH5α-T and BL21

  • The 4 μL of C-His Vector from stock is diluted with 16 μL of nuclease free water, then cut with E/P and purified from the gel.
  • Ligations
Ligation </font>
1. E. coli BL-21 KAH111(E/P)/size, 20 ng + C-His(E/P)/3600, 26ng KAH111/C-His 3:1 No Colonies
2. E. coli DH5α-T KAH111(E/P)/size, 16 ng + C-His(E/P)/3600, 26ng KAH111/C-His 3:1 No Colonies
3. E. coli BL-21 KAH112(E/P)/size, 22.8 ng + C-His(E/P)/3600, 26ng KAH112/C-His 3:1 No Colonies
4. E. coli DH5α-T KAH111(E/P)/size, 20 ng + C-His(E/P)/3600, 26ng KAH112/C-His 3:1 No Colonies
5. C-His(E/P)/ 26 ng (Control Plate)
  • Calculations are for the ng of insert we need to get a 3:1 ratio of insert molecules to 50 ng vector molecules
  1 2 3 4 5
Insert DNA 2.34 2.34 2.05 2.05 ---
Vector DNA 1.92 1.92 1.92 1.92 1.92
2x lgn buf (Roche) 5.26 5.26 5.0 5.0 5.0
T4 ligase (NEB) 1.0 1.0 1.0 1.0 1.0
dH2O 0 0 0.03 0.03 2.08
  10.52 μL 10.52 μL 10μl 10μL 10μL
  • The incubation time for the ligation process was 30min at room temperature.
  • Fast transformation, 30 min on ice.