Difference between revisions of "User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2012/12/01"

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(Autocreate 2012/12/01 Entry for User:Behzad_Damadzadeh/Notebook/PcTF_Subcloning_in_E-coli)
 
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=Date=
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=12/1/12=
  
'''List title'''
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> Digests (Fermentas FD)<br>
# List items
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PT7CFE1-CHis
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[[Image:Vector_Cut_(E-P).png‎ |thumb|350px|2 Human Vector PT7CFE1-CHis, 3600 bp, Cut with EcoRI and PstI Separately.]]
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{| class="wikitable" width=400px
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| Plasmid DNA || 3.0 μl*
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|-
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| EcoR1  || 1.0 μl
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|-
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| Pst1 || 1.0 μl
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|-
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| 10x FastDigest buffer + green loading dye || 1.5 μl
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|-
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| dH<sub>2</sub>O || 8.5 μl
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|-
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| &nbsp; || 15.0 μl total
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|-
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| Incubate at 37°C for 10 minutes.
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|}
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# Make the (1%) agarose glee and add 15μl  of restricted vector in one well and 10 μl  of ladder.

Revision as of 18:41, 2 December 2012

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12/1/12

> Digests (Fermentas FD)
PT7CFE1-CHis

2 Human Vector PT7CFE1-CHis, 3600 bp, Cut with EcoRI and PstI Separately.
Plasmid DNA 3.0 μl*
EcoR1 1.0 μl
Pst1 1.0 μl
10x FastDigest buffer + green loading dye 1.5 μl
dH2O 8.5 μl
  15.0 μl total
Incubate at 37°C for 10 minutes.
  1. Make the (1%) agarose glee and add 15μl of restricted vector in one well and 10 μl of ladder.