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Lab notes

introduction

control

communication

cohesion

completion

function test

introduction :P introduction :P introduction :P introduction :P

introduction of labnote

樹狀圖 timeline 順序圖

under construction

lab note of circuit in the completion part

Parts from iGEM took kit

Out line

For each part to be used in testing circuit:
BBa_J23100 , BBa_E1010, BBa_B0015

circuit 圖

After transforming these plasmids into our competent cell, DH5a, we would take 3 steps to examine if we got the right product:

Colony PCR and electrophoresis: Directly picking up colonies on designated antibiotic plate and do colony PCR with iGEM provided primers (VF2&VR), and then do electrophoresis to check the length of plasmid to confirm if the kit had been correctly transformed into E. coli.
Plasmid PCR and electrophoresis: Colony PCR may not end up copying the right place, for there is extra DNA in the cell that is not the one of our interest. Therefore, we also check the length of the plasmid we which we transformed.
Digestion and electrophoresis: After checking the length, we use EcoR1/Spe1 and Xba1/Pst1, and electrophoresis, to see if our constructed plasmid can be successfully digested.

Process

We encounter several difficulties during the process:

In the transformation step, we couldn’t get transformation with the right PCR band at first. Even thought they do grow on the antibiotic plate, electrophoresis result doesn’t show any band. Therefore, we tried different ways trying to solve these problems.
First, we thought it was PCR problem, therefore, we tried colony PCR. However, it came out that it wasn’t the case.So we improve our transformation protocol. That is, after 1.5 hour of recovery in 37C incubator in 200ml LB, we centrifuge in 3.4 rpm for 20 seconds, and discard 150ml supernatant.
At the end, we result in putting concentrated transformed E.coli into our antibiotic plate. This way, we sequentially transformed several kits successfully.
In the checking step, we’ve have contaminated electrophoresis result after colony PCR. That is, we got band in the negative well. To find out the ingredient causing contamination, we do several negative control changing different packing of ingredients. And find the contamination of our 10X DreamTaq Buffer.

@@ Line 109: / Line 109: @@
 <p>We encounter several difficulties during the process:</p>
 <ol>
-<li>1.	In the transformation step, we couldn’t get transformation with the right PCR band at first. Even thought they do grow on the antibiotic plate, electrophoresis result doesn’t show any band. Therefore, we tried different ways trying to solve these problems.<br>First, we thought it was PCR problem, therefore, we tried colony PCR. However, it came out that it wasn’t the case.So we improve our transformation protocol. That is, after 1.5 hour of recovery in 37C incubator in 200ml LB, we centrifuge in 3.4 rpm for 20 seconds, and discard 150ml supernatant.<br>At the end, we result in putting concentrated transformed E.coli into our antibiotic plate. This way, we sequentially transformed several kits successfully.</li>
+<li>In the transformation step, we couldn’t get transformation with the right PCR band at first. Even thought they do grow on the antibiotic plate, electrophoresis result doesn’t show any band. Therefore, we tried different ways trying to solve these problems.<br>First, we thought it was PCR problem, therefore, we tried colony PCR. However, it came out that it wasn’t the case.So we improve our transformation protocol. That is, after 1.5 hour of recovery in 37C incubator in 200ml LB, we centrifuge in 3.4 rpm for 20 seconds, and discard 150ml supernatant.<br>At the end, we result in putting concentrated transformed E.coli into our antibiotic plate. This way, we sequentially transformed several kits successfully.</li>
-<li>2.	In the checking step, we’ve have contaminated electrophoresis result after colony PCR. That is, we got band in the negative well. To find out the ingredient causing contamination, we do several negative control changing different packing of ingredients. And find the contamination of our 10X DreamTaq Buffer.</li>
+<li>In the checking step, we’ve have contaminated electrophoresis result after colony PCR. That is, we got band in the negative well. To find out the ingredient causing contamination, we do several negative control changing different packing of ingredients. And find the contamination of our 10X DreamTaq Buffer.</li>
 </ol>
           </div>

Team:NYMU-Taipei/notebook/labnotes

From 2014.igem.org

Revision as of 17:58, 28 September 2014

introduction :P introduction :P introduction :P introduction :P

lab note of circuit in the control part

experiment1 date: 0707~0712

experiment1 date: 0707~0712

experiment1 date: 0707~0712

lab note of circuit in the communication part

experiment1 date: 0707~0712

experiment1 date: 0707~0712

experiment1 date: 0707~0712

lab note of circuit in the cohesion part

experiment1 date: 0707~0712

experiment1 date: 0707~0712

experiment1 date: 0707~0712

lab note of circuit in the completion part

Parts from iGEM took kit

Out line

Process

lab note of function test in phage

experiment1 date: 0707~0712

experiment1 date: 0707~0712

experiment1 date: 0707~0712