Team:Technion/19 August 2012

From 2012.igem.org

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==Ilya==
==Ilya==
 +
- All the white colony PCR colonies were positive on the gel. I picked one from each clone and put a starter.
==Inbal==
==Inbal==
-
 
+
Today was pretty theoretical for me- I read and planned the Gibson assembly, Also I found out that it isn't piece of cake. <br>
 +
In addition, I measured the concentration of the mini preped pSB1C3+SP6 gene product:  105ng/ul.
==Asaf==
==Asaf==
Line 14: Line 16:
To do list: <br>
To do list: <br>
-
1. PCR for Chris's plasmids:  <br>
+
1. PCR for Chris's plasmids: promoter plasmids (5 total) <br>
-
2. PCR purification for PCR products of xyIE. <br>
+
 
 +
2. a. PCR purification for PCR products of xyIE. <br>
 +
2. b. Plates for plating the ligated products- with XXX antibiotic. <br>
 +
 
3. PCR purification for PCR products of Chris's plasmids. <br>
3. PCR purification for PCR products of Chris's plasmids. <br>
 +
 +
4. Restriction with XmaI + XhoI for: <br>
 +
-  xyIE PCR products  <br>
 +
-  Chris's promoter plasmids (5 reactions total) <br>
 +
 +
5. PCR purification for cut products of xyIE and Chris's plasmids  <br>
 +
 +
6. Ligation of xyIE and Chris's plasmids: 5 reactions total. <br>
 +
If there is time: PCR for alkaline phosphatase and running on Gel.
If there is time: PCR for alkaline phosphatase and running on Gel.
==Evgeni==
==Evgeni==

Latest revision as of 21:00, 22 August 2012



Team:Technion/19_August_2012
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Ilya

- All the white colony PCR colonies were positive on the gel. I picked one from each clone and put a starter.

Inbal

Today was pretty theoretical for me- I read and planned the Gibson assembly, Also I found out that it isn't piece of cake.
In addition, I measured the concentration of the mini preped pSB1C3+SP6 gene product: 105ng/ul.

Asaf

Hila

Lior

Noa

To do list:

1. PCR for Chris's plasmids: promoter plasmids (5 total)

2. a. PCR purification for PCR products of xyIE.
2. b. Plates for plating the ligated products- with XXX antibiotic.

3. PCR purification for PCR products of Chris's plasmids.

4. Restriction with XmaI + XhoI for:
- xyIE PCR products
- Chris's promoter plasmids (5 reactions total)

5. PCR purification for cut products of xyIE and Chris's plasmids

6. Ligation of xyIE and Chris's plasmids: 5 reactions total.

If there is time: PCR for alkaline phosphatase and running on Gel.

Evgeni

Shahar

Rachel