Team:Peking S/lab/notebook/sr

From 2011.igem.org

(Difference between revisions)
(Created page with "__NOTOC__ {{Template:Http://2011.igem.org/Team:Peking S/box4notebook}} * <span style="font-size:10mm"> <font color="#000033">'''Rui Sun's Notebook'''</font> </span> == '''s...")
(summary)
 
(17 intermediate revisions not shown)
Line 9: Line 9:
-
== '''summary''' ==
+
== '''Summary''' ==
-
blahblah...
+
In this summer, I mainly focused on the construction of the microbial population density balancer. In addition, I also carried out the assay for orthogonality of positive regulating signaling molecules.
=='''Contents'''==
=='''Contents'''==
Line 39: Line 39:
|style="text-align:center"| 1
|style="text-align:center"| 1
|style="text-align:center"| 2
|style="text-align:center"| 2
-
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.3|3]]
+
|style="text-align:center"| 3
|-  
|-  
-
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.4|4]]
+
|style="text-align:center"| 4
-
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.5|5]]
+
|style="text-align:center"| 5
-
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.6|6]]
+
|style="text-align:center"| 6
-
|style="text-align:center"| 7
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.7|7]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.8|8]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.8|8]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.9|9]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.9|9]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.10|10]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.10|10]]
|-  
|-  
-
|style="text-align:center"| 11
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.11|11]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.12|12]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.12|12]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.13|13]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.13|13]]
Line 55: Line 55:
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.15|15]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.15|15]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.16|16]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.16|16]]
-
|style="text-align:center"| 17
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.17|17]]
 +
 
|-  
|-  
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.18|18]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.18|18]]
Line 63: Line 64:
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.22|22]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.22|22]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.23|23]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.23|23]]
-
|style="text-align:center"| 24
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.24|24]]
|-  
|-  
-
|style="text-align:center"| 25
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.25|25]]
-
|style="text-align:center"| 26
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.26|26]]
-
|style="text-align:center"| 27
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.27|27]]
-
|style="text-align:center"| 28
+
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.28|28]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.29|29]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.29|29]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.30|30]]
|style="text-align:center"| [[Team:Peking_S/lab/notebook/yrf#7.30|30]]
Line 82: Line 83:
|}
|}
[<html><a href="#top">TOP</a></html>]
[<html><a href="#top">TOP</a></html>]
-
===7.3===
 
-
===7.4===
+
===7.7===
-
===7.5===
+
'''ABBREVIATIONS:
 +
 
 +
'''Restriction endonuleases:
 +
 
 +
'''E=EcoRI X=XbaI S=SpeI P=PstI'''''
 +
'''
 +
 
 +
 
 +
 
 +
17:30 Digestion of B0034(1-2M) with S&P and 4-12I with X&P started.
 +
      Fragment lengths: B0034  around 2000bps
 +
                        4-12I  756 bps
 +
      PCR of terminator-less version of Ptet-rhlI and lacI(I732011)-LVA
 +
 
 +
      Electroperesis:
 +
      Gel 1 Well 2-4: Marker_4-12I_1-2M
 +
      Gel 2 Well 2-5: Marker_rhlI_rhlI_rhlI
 +
      Gel 3 Well 1-6: Marker_lacI_lacI_ _ _lacI_lacI
 +
      All checked right.
 +
 
 +
      Gel extraction of the above DNA fragments.
 +
 
 +
      Ligation of B0034(SP digested)+4-12I(XP digested).
-
===7.6===
 
-
 
===7.8===
===7.8===
 +
 +
12:30  Transformation of the ligation product(1-2M+4-12I) finished.
 +
12:30  Gel extraction of PCR product (LacI-LVA) finished.
 +
 +
17:30  PCR for lacI-tag from I732100 started.
 +
 +
19:30  Transformation of 2-10G finished.
 +
     
 +
19:30  PCR failed. Repeated with the same system &condition and got the right string.
===7.9===
===7.9===
 +
0 :19  Checked plates.
 +
 +
0 :19  Gel extraction & PCR of lacI-LVA-suffix.
 +
 +
14:00  Digestion of 1-1G and lacI PCR product(second round) with X&P.
 +
 +
14:00  Colony pick of 1-1G plates.
 +
 +
18:30  Electrophoresis for digestion products(1-1G XP fragment;lacI PCR product digested with X&P).
 +
 +
23:45  Ligation of 1-1G and lacI-suffix fragments started.
===7.10===
===7.10===
 +
00:05  Digestion of Ptet-rhlI PCR products (1 and 2) started.
 +
00:05  Digestions: 2-10G(EX) 1-2M+4-12I(RBS+gfp-LVA)(1,2,3,ES)  1-23L(EX&ES) started.
===7.12===
===7.12===
Line 105: Line 147:
===7.16===
===7.16===
 +
 +
===7.17===
===7.18===
===7.18===
Line 117: Line 161:
===7.23===
===7.23===
 +
 +
===7.24===
 +
 +
===7.25===
 +
 +
===7.26===
 +
 +
===7.27===
 +
 +
===7.28===
===7.29===
===7.29===
Line 123: Line 177:
===7.31===
===7.31===
-
 
==August==
==August==

Latest revision as of 05:20, 5 October 2011


Template:Https://2011.igem.org/Team:Peking S/bannerhidden


无标题文档

css r corner


  • Rui Sun's Notebook


Summary

In this summer, I mainly focused on the construction of the microbial population density balancer. In addition, I also carried out the assay for orthogonality of positive regulating signaling molecules.

Contents

July

Mon Tue Wed Thu Fri Sat Sun
- - - - 1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30 31
- - - - - - -

[TOP]

7.7

ABBREVIATIONS:

Restriction endonuleases:

E=EcoRI X=XbaI S=SpeI P=PstI


17:30 Digestion of B0034(1-2M) with S&P and 4-12I with X&P started.

     Fragment lengths: B0034  around 2000bps
                       4-12I  756 bps
     PCR of terminator-less version of Ptet-rhlI and lacI(I732011)-LVA
     Electroperesis:
     Gel 1 Well 2-4: Marker_4-12I_1-2M
     Gel 2 Well 2-5: Marker_rhlI_rhlI_rhlI
     Gel 3 Well 1-6: Marker_lacI_lacI_ _ _lacI_lacI
     All checked right.
     Gel extraction of the above DNA fragments.
     Ligation of B0034(SP digested)+4-12I(XP digested).

7.8

12:30 Transformation of the ligation product(1-2M+4-12I) finished. 12:30 Gel extraction of PCR product (LacI-LVA) finished.

17:30 PCR for lacI-tag from I732100 started.

19:30 Transformation of 2-10G finished.

19:30 PCR failed. Repeated with the same system &condition and got the right string.

7.9

0 :19 Checked plates.

0 :19 Gel extraction & PCR of lacI-LVA-suffix.

14:00 Digestion of 1-1G and lacI PCR product(second round) with X&P.

14:00 Colony pick of 1-1G plates.

18:30 Electrophoresis for digestion products(1-1G XP fragment;lacI PCR product digested with X&P).

23:45 Ligation of 1-1G and lacI-suffix fragments started.

7.10

00:05 Digestion of Ptet-rhlI PCR products (1 and 2) started. 00:05 Digestions: 2-10G(EX) 1-2M+4-12I(RBS+gfp-LVA)(1,2,3,ES) 1-23L(EX&ES) started.

7.12

7.13

7.14

7.15

7.16

7.17

7.18

7.19

7.20

7.21

7.22

7.23

7.24

7.25

7.26

7.27

7.28

7.29

7.30

7.31

August

Mon Tue Wed Thu Fri Sat Sun
1 2 3 4 5 6 7
8 9 10 11 12 13 14
15 16 17 18 19 20 21
22 23 24 25 26 27 28
29 30 31 - - - -

[TOP]

8.1

8.2

8.4

8.5

8.6

8.7

8.8

8.9

8.10

8.11

8.12

8.13

8.14

8.15

8.16

8.17

8.18

8.19

8.20

8.21

8.22

8.23

8.25

8.26

8.27

8.30

8.31

September

Mon Tue Wed Thu Fri Sat Sun
- - 1 2 3 4
5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30 - --

[TOP]

9.1

9.2

9.3

9.6

9.7

9.8

9.9

9.12

9.13

9.14

9.15

9.16

9.17

9.21

9.22

9.23

9.24

9.25

9.26

9.27

9.28

9.29

9.30

October

Mon Tue Wed Thu Fri Sat Sun
- - - - 1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 - - - - - -

[TOP]

10.1

10.3

10.4

10.5

10.7

10.8

10.9

10.10

10.11

10.12

10.13

10.15

10.16-10.21

10.21-10.25



</html>