User:Karmella Haynes/Notebook/BioBrick cloning/2012/12/11

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(Autocreate 2012/12/11 Entry for User:Karmella_Haynes/Notebook/BioBrick_cloning)
Current revision (14:27, 12 December 2012) (view source)
(12/11/12)
 
(10 intermediate revisions not shown.)
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| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
-
==mm/dd/yy==
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==12/11/12==
<!-- Precede finished items with a checkmark &#x2713; -->
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* Line item 1
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* Note: colonies from retransformation of pSB1A3-RFP look red
-
* Line item 2
+
* Assembly: KAH111 + C-His (trouble shooting for Behzad, start from plasmids)
 +
* Minipreps: Rene's pSB1A3-RFP (2); cut with X/S for Brady and Vi's Gibson cloning
-
----
 
-
'''Minipreps'''<br>
 
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* Check with E/P digests
 
-
 
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{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
 
-
|- valign="top"
 
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| bgcolor=#cfcfcf | Reagent
 
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| bgcolor=#cfcfcf | Volume
 
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| rowspan="7" | <u>Expected:</u><br>1. BB 1 = size<br>2. BB2 = size<br>
 
-
| rowspan="7" | <!-- [[Image:GelImage.jpg|400px|Hover name]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] -->
 
-
|-
 
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| DNA(plasmid) || 2.0 μL
 
-
|-
 
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| 10X buffer || 1.5
 
-
|-
 
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| EcoRI || 1.0
 
-
|-
 
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| PstI || 1.0
 
-
|-
 
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| dH<sub>2</sub>O || 9.5
 
-
|-
 
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| &nbsp; || 15 μL --> 37°C/ ~15 min.
 
-
|}
 
----
----
'''Assemblies'''
'''Assemblies'''
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# BioBrick name: 5' part/(a/b)/size + 3' part/(c/d)/size
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# KAH111/C-His: 5' part/(E/P)/1123 + C-His/(E/P)/3600
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# BioBrick name: 5' part/(a/b)/size + 3' part/(c/d)/size
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* Digests (Fermentas FD)
* Digests (Fermentas FD)
-
** Specific notes
 
{| {{table}} cellspacing="3" <!-- Digest rxn. table -->
{| {{table}} cellspacing="3" <!-- Digest rxn. table -->
Line 49: Line 25:
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Volume
| bgcolor=#cfcfcf | Volume
-
| rowspan="7" | <!-- [[Image:GelImage.jpg|270px|Hover name]]<br>30 μL/lane, 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder] -->
+
| rowspan="7" | [[Image:KAH121112_gel2.png|200px|Hover name]]<br>30 μL/lane, 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder]
|-
|-
-
| DNA (plasmid) || up to 25 μL
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| DNA (plasmid) || 15.0 μL
|-
|-
| 10x buffer || 3.0
| 10x buffer || 3.0
Line 59: Line 35:
| enzyme 2 || 1.0
| enzyme 2 || 1.0
|-
|-
-
| dH<sub>2</sub>O || ---
+
| dH<sub>2</sub>O || 10.0
|-
|-
| &nbsp; || 30 μL --> 37°C/ ~30 min.
| &nbsp; || 30 μL --> 37°C/ ~30 min.
Line 65: Line 41:
-
* Measure conc.'s
+
* Measure conc.'s of DNA purified from gel (Zymo kit)
{| {{table}} cellspacing="3" <!-- [DNA] table -->
{| {{table}} cellspacing="3" <!-- [DNA] table -->
|- bgcolor=#cfcfcf  
|- bgcolor=#cfcfcf  
| Sample || OD260 || 260/280 || ng/μL
| Sample || OD260 || 260/280 || ng/μL
|-
|-
-
| 1. Digested part (a/b) || --- || --- || ---
+
| 1. KAH11 (E/P) || 0.019 || 1.96 || 18.7
|-
|-
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| 2. Digested part (c/d) || --- || --- || ---
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| 2. C-His (E/P) || 0.047 || 1.82 || 46.8
-
|}
+
-
 
+
-
 
+
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* Dephosphorylation (Roche)
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{| {{table}} cellspacing="3" <!-- Dephos table -->
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-
|-
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| bgcolor=#cfcfcf | Reagent
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| bgcolor=#cfcfcf | Volume
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|-
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| DNA (clean digest) || up to 17 μL (500 ng)
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-
|-
+
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| 10x buffer d.p. || 2.0
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-
|-
+
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| phosphatase || 1.0
+
-
|-
+
-
| dH<sub>2</sub>O || ---
+
-
|-
+
-
| &nbsp; || 20 μL --> 37°C/ 10 min.; 75°C/ 2 min.; [final] = 25 ng/μL
+
|}
|}
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{| {{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> mm/dd/yy</font>
+
| Ligation || <font color="blue"><u>Plate results (lig : neg crtl)</u> 12/12/12</font>
|-
|-
-
| 1. insert(a/b)/size, ## ng + vector(c/d)/size, ## ng || <font color="blue">new BioBrick #:1 (Pick #)</font>
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| 1. KAH111(E/P)/size, 16 ng + C-His(E/P)/3600, 25ng || <font color="blue">KAH111/C-His 3:1 (Pick 4)</font> (very small colonies after ~18 hours)
|-
|-
-
| 2. vector(c/d)/ ## ng || &nbsp;
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| 2. C-His(E/P)/ 25 ng || 3 colonies
|}
|}
{| {{table}} cellspacing="3" <!-- Ligation rxn table -->
{| {{table}} cellspacing="3" <!-- Ligation rxn table -->
-
| &nbsp;            || 1    || 2   ||
+
| &nbsp;            || 1    || 2  
|-
|-
-
| Insert DNA        || ### || ---  ||
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| Insert DNA        || 1.0 || ---   
|-
|-
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| Vector DNA        || ### || ### ||
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| Vector DNA        || 0.5 || 0.5  
|-
|-
-
| 2x lgn buf (Roche) || ###  || ### ||
+
| 2x lgn buf (Roche) || 5.0 || 5.0
|-
|-
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| T4 ligase (NEB)    || 1.0  || 1.0  ||
+
| T4 ligase (NEB)    || 1.0  || 1.0   
|-
|-
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| dH<sub>2</sub>O    || ### || ### ||
+
| dH<sub>2</sub>O    || 2.5 || 3.5  
|-
|-
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| &nbsp;            || # μL || # μL ||
+
| &nbsp;            || 10 μL || 10 μL  
|}
|}
 +
 +
----
----
-
'''Oligo annealing'''
+
'''Minipreps'''<br>
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# New BB 1
+
* pSB1A3-RFP (retransformation from 12/10/12)
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# New BB 2
+
* Note: pellets are red
 +
* Digest 10 μL of each with X/S for Gibson cloning (Brady and Vi)
 +
* Note: combined mini preps afterwards; concentration = 60 ng/μL
-
{| class="wikitable" border="0" cellspacing="3" <!-- Oligo annealing rxn table -->
+
{| {{table}} border="1" cellspacing="3" <!-- Digest check rxn. table -->
-
| DNA (oligos, 100 μM) || up to 18 μL (3 μL ea.)
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|- valign="top"
 +
| bgcolor=#cfcfcf | Reagent
 +
| bgcolor=#cfcfcf | Volume
 +
| rowspan="7" | <u>Expected:</u><br>3. pSB1A3 = 2155<br>4. pSB1A3 = 2155<br>
 +
| rowspan="7" | [[Image:KAH121112_gel1.png|200px|Hover name]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder]
|-
|-
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| 10x annealing buffer || 2.0
+
| DNA(plasmid) || 10.0 μL
|-
|-
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| dH<sub>2</sub>O || ---
+
| 10X buffer || 3.0
|-
|-
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| &nbsp; || 20 μL --> 100°C (water bath)/ 5 min.; Cool to R.T. overnight
+
| XbaI || 1.0
 +
|-
 +
| SpeI || 1.0
 +
|-
 +
| dH<sub>2</sub>O || 15.0
 +
|-
 +
| &nbsp; || 15 μL --> 37°C/ ~30 min.
|}
|}
 +
 +
 +
* Gel purification: combined the two slices
 +
** Concentration: 260 = 0.015, 260/280 = 2.2, '''ng/μL = 15.1'''

Current revision

Karmella's BioBrick Cloning Main project page
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12/11/12

  • Note: colonies from retransformation of pSB1A3-RFP look red
  • Assembly: KAH111 + C-His (trouble shooting for Behzad, start from plasmids)
  • Minipreps: Rene's pSB1A3-RFP (2); cut with X/S for Brady and Vi's Gibson cloning



Assemblies

  1. KAH111/C-His: 5' part/(E/P)/1123 + C-His/(E/P)/3600


  • Digests (Fermentas FD)
Reagent Volume Hover name
30 μL/lane, 1% agarose; Ladder
DNA (plasmid) 15.0 μL
10x buffer 3.0
enzyme 1 1.0
enzyme 2 1.0
dH2O 10.0
  30 μL --> 37°C/ ~30 min.


  • Measure conc.'s of DNA purified from gel (Zymo kit)
Sample OD260 260/280 ng/μL
1. KAH11 (E/P) 0.019 1.96 18.7
2. C-His (E/P) 0.047 1.82 46.8


  • Ligations
Ligation Plate results (lig : neg crtl) 12/12/12
1. KAH111(E/P)/size, 16 ng + C-His(E/P)/3600, 25ng KAH111/C-His 3:1 (Pick 4) (very small colonies after ~18 hours)
2. C-His(E/P)/ 25 ng 3 colonies
  1 2
Insert DNA 1.0 ---
Vector DNA 0.5 0.5
2x lgn buf (Roche) 5.0 5.0
T4 ligase (NEB) 1.0 1.0
dH2O 2.5 3.5
  10 μL 10 μL



Minipreps

  • pSB1A3-RFP (retransformation from 12/10/12)
  • Note: pellets are red
  • Digest 10 μL of each with X/S for Gibson cloning (Brady and Vi)
  • Note: combined mini preps afterwards; concentration = 60 ng/μL
Reagent Volume Expected:
3. pSB1A3 = 2155
4. pSB1A3 = 2155
Hover name
15 μL/lane; 1% agarose; Ladder
DNA(plasmid) 10.0 μL
10X buffer 3.0
XbaI 1.0
SpeI 1.0
dH2O 15.0
  15 μL --> 37°C/ ~30 min.


  • Gel purification: combined the two slices
    • Concentration: 260 = 0.015, 260/280 = 2.2, ng/μL = 15.1



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