User:Cassandra M Barrett/Notebook/Open Chromatin/2015/11/29: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
(Autocreate 2015/11/29 Entry for User:Cassandra_M_Barrett/Notebook/Open_Chromatin)
 
Line 6: Line 6:
| colspan="2"|
| colspan="2"|
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
<!-- ##### DO NOT edit above this line unless you know what you are doing. ##### -->
==Entry title==
==pJET Sequence Results==
* Insert content here...


Purpose: to evaluate sequences from pJET vector in order to determine success of LCR troubleshooting experiment
Results:
Sequences from the five pJET colonies were determined using sequencing primers just outside of the insertion site.
Colony 1 resulted in essentially no homologous sequences either with the forward or reverse primer. Colonies 2 and 3 showed homology with the ATF2 domain, which appears to have inserted on its own in both cases. Both colony 5 reactions failed. Colony 4 forward reaction gave week homology to part of the MV10 vector backbone??? and the reverse reaction was homologous to the ampicillin resistance marker and bla promoter? Possible cross reaction with sequencing primers on the pJET backbone or contamination.
Conclusions:
The LCR troubleshooting experiment yielded only negative results. Some of one part inserted into the pJET vector, but no annealed parts did. We had low transformation levels to begin with as well...probably time to move on to Gibson assembly.


<!-- ##### 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. ##### -->

Revision as of 12:18, 29 November 2015

Project name <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>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;</html>Next entry<html><img src="/images/5/5c/Resultset_next.png" border="0" /></html>

pJET Sequence Results

Purpose: to evaluate sequences from pJET vector in order to determine success of LCR troubleshooting experiment

Results:

Sequences from the five pJET colonies were determined using sequencing primers just outside of the insertion site.

Colony 1 resulted in essentially no homologous sequences either with the forward or reverse primer. Colonies 2 and 3 showed homology with the ATF2 domain, which appears to have inserted on its own in both cases. Both colony 5 reactions failed. Colony 4 forward reaction gave week homology to part of the MV10 vector backbone??? and the reverse reaction was homologous to the ampicillin resistance marker and bla promoter? Possible cross reaction with sequencing primers on the pJET backbone or contamination.

Conclusions:

The LCR troubleshooting experiment yielded only negative results. Some of one part inserted into the pJET vector, but no annealed parts did. We had low transformation levels to begin with as well...probably time to move on to Gibson assembly.