User:Behzad Damadzadeh/Notebook/PcTF Subcloning in E-coli/2012/04/05: Difference between revisions
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> Digests (Fermentas FD)<br> | > Digests (Fermentas FD)<br> | ||
[[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 | {| class="wikitable" width=400px | ||
| Plasmid DNA || 2.0 μl* | | Plasmid DNA || 2.0 μl* | ||
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| || 15.0 μl total | | || 15.0 μl total | ||
|- | |- | ||
| Incubate at 37°C for | | 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. | # 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 09:53, 11 April 2012
PcTF Subcloning in E. coli | <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page <html><img src="/images/c/c3/Resultset_previous.png" border="0" /></html>Previous entry<html> </html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html> | |||||||||||||
5/4/2012Culturing the colonies grew on agar plates on 4/4/2012
Grow liquid cultures
Extract the plasmid DNA: Qiagen Miniprep Kit' 1.5 hours Biotek Take3 Result:
Confirm the assembly Check the plates, grow cultures, and do minipreps 6 hours
> Digests (Fermentas FD)
'The size of the constructed gene supposed to be: 1123 + 15 + 6 = 1144 bp' |