Haynes Lab:Notebook/Investigating Photo-Switchable Synthetic Nucleosomes/2012/11/06

From OpenWetWare

Jump to: navigation, search
(→November 6, 2012)
Current revision (05:52, 14 November 2012) (view source)
(→November 6, 2012)
 
(12 intermediate revisions not shown.)
Line 15: Line 15:
  ! scope="col" style="background:#efefef;" | H2B-GFP/EcoRI
  ! scope="col" style="background:#efefef;" | H2B-GFP/EcoRI
  ! scope="col" style="background:#efefef;" | H2B-GFP/PstI
  ! scope="col" style="background:#efefef;" | H2B-GFP/PstI
-
  ! scope="col" style="background:#efefef;" | LOV/EcoRI
+
  ! scope="col" style="background:#efefef;" | LOV/PstI
  |-
  |-
  |DNA(plasmid)   
  |DNA(plasmid)   
Line 30: Line 30:
  |1.0
  |1.0
  |0
  |0
-
  |1.0
+
  |0
  |-
  |-
  |PstI
  |PstI
  |0
  |0
  |1.0
  |1.0
-
  |0
+
  |1.0
  |-
  |-
  |dH<sub>2</sub>O
  |dH<sub>2</sub>O
Line 48: Line 48:
  |}
  |}
-
[[Image:VN_Gel_11-6-12.png|thumb|frame|center|150px|Results of the digests are shown.]]
+
 
 +
{| class="wikitable" border=0
 +
|-
 +
| <u>Expected:</u><br>1. H2B-GFP/ EcoRI = 4885, 210 <br>2. H2B-GFP/ PstI = 5101<br>3. LOV/PstI = 251
 +
| <br>
 +
|}
 +
 
 +
<center>
 +
[[Image:VN_Gel_11-6-12.png|150px|Results of the digests are shown.]]
 +
[[Image:KAH_Fermentas_GeneRuler_1kbplus.jpg]]
 +
</center>
 +
 
 +
<center>
 +
Results of the digests are shown.
 +
</center>
 +
 
 +
----
 +
*'''[[User:Karmella Haynes|---Karmella]] 16:01, 7 November 2012 (EST)''': Note: Please re-do LOV/PstI
 +
<br>
 +
 
 +
*'''[[User:Karmella Haynes|---Karmella]] 16:01, 7 November 2012 (EST)''': Here is a reaction table for PCR
 +
 
 +
* First, resuspend dry primer oligos (in blue-capped tubes) to 100 μM
 +
* Then make working solutions of 10 μM
 +
* Reactions:
 +
 
 +
# H2B-GFP plasmid + BB_H2B fwd + BB_H2B rev
 +
# LOV plasmid + BB_LOV fwd + BB_LOV rev
 +
 
 +
{| class="wikitable" border=1 cellpadding="5" cellspacing="0"
 +
|-
 +
| Reagents || H2B || LOV
 +
|-
 +
| Plasmid DNA || 0.5 μL || 0.5
 +
|-
 +
| primer 1 (10 μM) || 1.0 || 1.0
 +
|-
 +
| primer 2 (10 μM) || 1.0 || 1.0
 +
|-
 +
| 2x GoTaq mix || 12.5 || 12.5
 +
|-
 +
| dH<sub>2</sub>O || 10.5 || 10.5
 +
|}
 +
 
 +
PCR program:
 +
* 95°C, 3 min.
 +
* [95°C, 30 sec; 57°C, 30 sec.; 72°C, 30 sec.] x35 cycles
 +
* 72°C, 3 min.
 +
* 4°C ∞
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit below this line unless you know what you are doing. ##### -->

Current revision

Project name Main project page
Previous entry      Next entry

November 6, 2012

  • Restriction digests of H2B-GFP and LOV
Restriction Digest Reagents
Reagent H2B-GFP/EcoRI H2B-GFP/PstI LOV/PstI
DNA(plasmid) 2.0 2.0 2.0
10x buffer 1.5 1.5 1.5
EcoRI 1.0 0 0
PstI 0 1.0 1.0
dH2O 10.5 10.5 10.5
Total 15.0 15.0 15.0


Expected:
1. H2B-GFP/ EcoRI = 4885, 210
2. H2B-GFP/ PstI = 5101
3. LOV/PstI = 251

Results of the digests are shown. Image:KAH_Fermentas_GeneRuler_1kbplus.jpg

Results of the digests are shown.

  • ---Karmella 16:01, 7 November 2012 (EST): Note: Please re-do LOV/PstI


  • ---Karmella 16:01, 7 November 2012 (EST): Here is a reaction table for PCR
  • First, resuspend dry primer oligos (in blue-capped tubes) to 100 μM
  • Then make working solutions of 10 μM
  • Reactions:
  1. H2B-GFP plasmid + BB_H2B fwd + BB_H2B rev
  2. LOV plasmid + BB_LOV fwd + BB_LOV rev
Reagents H2B LOV
Plasmid DNA 0.5 μL 0.5
primer 1 (10 μM) 1.0 1.0
primer 2 (10 μM) 1.0 1.0
2x GoTaq mix 12.5 12.5
dH2O 10.5 10.5

PCR program:

  • 95°C, 3 min.
  • [95°C, 30 sec; 57°C, 30 sec.; 72°C, 30 sec.] x35 cycles
  • 72°C, 3 min.
  • 4°C ∞


Retrieved from "http://www.openwetware.org/wiki/Haynes_Lab:Notebook/Investigating_Photo-Switchable_Synthetic_Nucleosomes/2012/11/06"
Personal tools