Team:Arizona State/Notebook/PCRLog

From 2011.igem.org

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==Primer Round 1==
==Primer Round 1==
===July 17, 2011===
===July 17, 2011===
-
<b>CasABCDE</b>: Touchdown PCR, Start Temp 70, -0.2 / cycle, Final Temp 64</p>
+
<b>CasABCDE</b>: Touchdown PCR, Start Temp 70, -0.2 / cycle, Final Temp 64
-
<br><b>Cas3</b>: Touchdown PCR, Start Temp 63, -0.2 / cycle, Final Temp 57</p>
+
<br><b>Cas3</b>: Touchdown PCR, Start Temp 63, -0.2 / cycle, Final Temp 57
<p>Gel Results:</p>
<p>Gel Results:</p>
-
[[Image:]]
+
[[Image:ASU_717_cas_gel.jpg|300px]]
<br>CasABCDE: Very faint bands near target length
<br>CasABCDE: Very faint bands near target length
<br>Cas3: No bands
<br>Cas3: No bands
 +
 +
===July 18, 2011===
 +
<b>CasABCDE</b>: Touchdown PCR, Start Temp 65, -0.2 / cycle, Final Temp 59
 +
<p>Gel Results:</p>
 +
<br>CasABCDE: No bands
 +
 +
===July 19, 2011===
 +
<b>CasABCDE</b>: Touchdown PCR, Start Temp 70, -0.2 / cycle, Final Temp 63
 +
<br><b>Cas3</b>: Temp gradient with 3 rows from 72 to 55 (L to R: 55, 61.7, 71)
 +
<br>Gel Results:
 +
<br>[[Image:ASU_719_casABCDE.jpg|300px]]
 +
<br>CasABCDE: Clearer bands around target length, primer dimers
 +
<br>[[Image:ASU_719_cas3.jpg|300px]]
 +
<br>Cas3: Middle temperature was optimal, clear bands are visible (likely correct length, failed to run a hyperladder), primer dimers
 +
 +
===July 20, 2011===
 +
<b>CasABCDE</b>: Touchdown PCR, Start Temp 71, -0.2 / cycle, Final Temp 64
 +
<br><b>Cas3</b>: Gradient using tighter range around best temp from yesterday (65.6, 63.1, 61.2, 58.5)
 +
<p>Gel Results:</p>
 +
[[Image:]]
 +
<br>CasABCDE: Nonspecific, nothing usable, no bands in target range, dimerization
 +
[[Image:]]
 +
<br>Cas3: Small band at correct location, primer dimers
 +
 +
===July 24, 2011===
 +
<p>PCR of CasABCDE, Cas3 with new settings; Preparation for extraction, "PCRception" (PCRing the PCR results); Included an elongation step in each cycle, which was not done for the previous runs; Settings stored in PCR machine as ABCDE724, CAS3724
 +
</p>
 +
<b>CasABCDE Settings and Results</b>:
 +
<br>[[Image:]]
 +
<br>[[Image:]]
 +
<br>Nonspecific results, perhaps a hint of the correct bands in the second to last well
 +
<br><b>Cas3 Settings and Results</b>:
 +
<br>[[Image:]]
 +
<br>[[Image:]]
 +
<br>Success for Cas3!! Extracted the band that lies around ~2500 (target is 2600). However, sequencing results were never conclusive and the sample was lost.
==Primer Round 2==
==Primer Round 2==

Revision as of 21:50, 28 September 2011


PCR Log for E. Coli Cas Genes


ASU Logo.png

Overview

This logbook is a record of the majority of our attempts to PCR amplify CRISPR-associated (Cas) ABCDE and Cas 3 of E. coli K12 MG1655. The record begins after our attempt to individually PCR amplify each of the 6 genes, which was unsuccessful. Here, three different sets of primers were used to attempt PCR amplification of the Cas genes in two sections.

Notes

Suggested annealing temperatures are based on [http://www.neb.com/nebecomm/tech_reference/TmCalc/Default.asp NEB Tm Calculator], as called for in the [http://www.neb.com/nebecomm/tech_reference/polymerases/phusion_high.asp?&utm_source=Google&utm_medium=CPC&utm_term=+phusion&utm_campaign=Phusion NEB Phusion DNA Polymerase] protocol.

Desired band for CasABCDE at ~4300bp

Desired band for Cas3 at ~2667bp

Primer Round 1

July 17, 2011

CasABCDE: Touchdown PCR, Start Temp 70, -0.2 / cycle, Final Temp 64
Cas3: Touchdown PCR, Start Temp 63, -0.2 / cycle, Final Temp 57

Gel Results:

ASU 717 cas gel.jpg
CasABCDE: Very faint bands near target length
Cas3: No bands

July 18, 2011

CasABCDE: Touchdown PCR, Start Temp 65, -0.2 / cycle, Final Temp 59

Gel Results:


CasABCDE: No bands

July 19, 2011

CasABCDE: Touchdown PCR, Start Temp 70, -0.2 / cycle, Final Temp 63
Cas3: Temp gradient with 3 rows from 72 to 55 (L to R: 55, 61.7, 71)
Gel Results:
ASU 719 casABCDE.jpg
CasABCDE: Clearer bands around target length, primer dimers
ASU 719 cas3.jpg
Cas3: Middle temperature was optimal, clear bands are visible (likely correct length, failed to run a hyperladder), primer dimers

July 20, 2011

CasABCDE: Touchdown PCR, Start Temp 71, -0.2 / cycle, Final Temp 64
Cas3: Gradient using tighter range around best temp from yesterday (65.6, 63.1, 61.2, 58.5)

Gel Results:

[[Image:]]
CasABCDE: Nonspecific, nothing usable, no bands in target range, dimerization [[Image:]]
Cas3: Small band at correct location, primer dimers

July 24, 2011

PCR of CasABCDE, Cas3 with new settings; Preparation for extraction, "PCRception" (PCRing the PCR results); Included an elongation step in each cycle, which was not done for the previous runs; Settings stored in PCR machine as ABCDE724, CAS3724

CasABCDE Settings and Results:
[[Image:]]
[[Image:]]
Nonspecific results, perhaps a hint of the correct bands in the second to last well
Cas3 Settings and Results:
[[Image:]]
[[Image:]]
Success for Cas3!! Extracted the band that lies around ~2500 (target is 2600). However, sequencing results were never conclusive and the sample was lost.

Primer Round 2

==Primer Round 3==