Difference between revisions of "User:Wesley J. Houston/Notebook/MAP/2013/02/08"

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(February 8, 2013)
(February 8, 2013)
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| <u>Ligation</u> || <font color="blue"><u>Plate results (lig : neg crtl)</u> 02/20/13</font>
 
| <u>Ligation</u> || <font color="blue"><u>Plate results (lig : neg crtl)</u> 02/20/13</font>
 
|-
 
|-
| 1. KAH201 (S/P)/<font color="blue">3403, 25 ng + KAH182 (X/P)/1675, # ng || <font color="blue">0</font>
+
| 1. KAH201 (S/P)/<font color="blue">3403</font>, 25 ng + KAH182 (X/P)/1675, # ng || <font color="blue">0</font>
 
|-
 
|-
 
| 2. KAH201 (X/P)/3403, 25 ng || 0
 
| 2. KAH201 (X/P)/3403, 25 ng || 0

Revision as of 10:50, 4 March 2013

Owwnotebook icon.png Building a Reporter Gene <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
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February 8, 2013

  • Assembly: (5xGal4 : [Spacer : HSVtk TATA]) : (K : AmCyan : AmCyan : NLS : STOP : [polyA2]) (KAH201)/(KAH182); AmCyan reporter gene for chromatin proteins.



Assemblies

  • Note, KAH201 is in vector V0120, so add 3200 bp to the size.
  1. KAH201/KAH182: (1) KAH201/(S/P)/203+3200 + (2) KAH182/(X/P)/1675

> Digests (Fermentas FD)


Reagent Volume   Placeholder Image
30 μL/lane, 1% agarose; Ladder
DNA (plasmid) 20 μL
10x buffer 3.0
enzyme 1 1.0
enzyme 2 1.0
dH2O 5.0 μL
  30 μL --> 37°C/ ~15 min.


> Measure conc.'s of gel purified fragments

Sample OD260 260/280 ng/μL
1. KAH201 (S/P) 0.048 1.88 48.1
2. KAH182 (X/P) 0.008 1.93 8.1


> Ligations

Ligation Plate results (lig : neg crtl) 02/20/13
1. KAH201 (S/P)/3403, 25 ng + KAH182 (X/P)/1675, # ng 0
2. KAH201 (X/P)/3403, 25 ng 0
  1 2
Insert DNA 0.74 ---
Vector DNA 0.52 0.52
2x lgn buf (Roche) 5.0 5.0
T4 ligase (NEB) 1.0 1.0
dH2O 2.74 3.48
  10 μL 10 μL
  • Follow quick transformation protocol
  • Add 30 uL DH5α-Turbo to each ligation; plate on 100 μg/mL Amp agar
  • No colonies were formed, this will be repeated. See 2/26/13 entry.