User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2012/04/11: Difference between revisions

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=Date=
=11/4/12=


'''List title'''
> Digests (Fermentas FD)<br>
# List items
BD-112 and BD-113
 
[[Image:BD-111-Behzad-5-4-12.jpg|thumb|350px|White dashed lines border show the vector backbone and the BD-111 constructed gene(RBS + PcTF).]]
{| class="wikitable" width=400px
| Plasmid DNA || 2.0 μl*
|-
| EcoR1  || 1.0 μl
|-
| Pst1 || 1.0 μl
|-
| 10x FastDigest buffer + green loading dye || 1.5 μl
|-
| dH<sub>2</sub>O || 9.5 μl
|-
| &nbsp; || 15.0 μl total
|-
| Incubate at 37°C for 10 minutes.
|}
 
# Make the (1%) agarose glee and add 15μl  of restricted DNA (PcTF & RBS) in one well and 10 μl  of ladder.
'The size of the constructed gene supposed to be: 1123 + 15 + 6 = 1144 bp'

Revision as of 10:00, 11 April 2012

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11/4/12

> Digests (Fermentas FD)
BD-112 and BD-113

White dashed lines border show the vector backbone and the BD-111 constructed gene(RBS + PcTF).
Plasmid DNA 2.0 μl*
EcoR1 1.0 μl
Pst1 1.0 μl
10x FastDigest buffer + green loading dye 1.5 μl
dH2O 9.5 μl
  15.0 μl total
Incubate at 37°C for 10 minutes.
  1. Make the (1%) agarose glee and add 15μl of restricted DNA (PcTF & RBS) in one well and 10 μl of ladder.

'The size of the constructed gene supposed to be: 1123 + 15 + 6 = 1144 bp'

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