Week of 7/26

From 2010.igem.org

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Latest revision as of 19:54, 23 October 2010

July 26th

Colony PCR:

 -J24679+B1002+K3
 -J24679+B1006+K3
 -Lux+RBS+B1006+K3 redo
 -Lux+RBS+B1002+K3

Digests:

 -Lux+RBS (EP)
 -A3 (EP+Phosphatase)

Ligations:

 -Lux+RBS+A3

Gel Order:

 -Ladder
 -J24679+B1002+K3 (A-E)
 -J24679+B1006+K3 (A-E)

The bands for 1B and 1D showed up so they were grown up accordingly.

July 27th

Digests:

 - C0261 (ES)
 - R0010 (ES)
 - J23100(ES)
 - J24679(XP)
 - P0451 (XP)
 - LuxR+RBS (XP)

The colony PCR that was done yesterday was ran on a gel. The gel order is as follows:

- Ladder
- J24679+B1006+K3 (E)
- Lux+RBS+B1006+K3 redo (A-E)
- Lux+RBS+B1002+K3 (A-E)

A second gel was ran from the digests that were done today. The gel order is provided below:

-Ladder
-pSB1T3 yellow
-pJ241
-A-E

Items sent to sequencing:

Sent to sequencing:

1) J24679+B1002 B (Reverse)
2) J24679+B1002 D (Reverse)
3) LuxR+RBS+A3 C (Forward+Reverse)
4) LuxR+RBS+A3 A (Forward+Reverse)

Grow for tomorrow:

-C0261
-J23100
-pJ241
-pSB1T3 yellow

All 3 pigments were streaked onto the plate to make new stocks.

Only pJ241 was ligated because there was a top and bottom band and we were not sure which was the actual pigment we extracted.

July 28th

Colony PCR Gel:

- Ladder
-13A-E
-14A-D
 13: P0451+R0010
 14: J23100+LuxR+RBS

Since 13B and C grew, we sent those to sequencing with forward and reverse primers. Lux+RBS+A3 was also sent to sequencing with the same primers.

We also grew up pSB1T3 red, pSB1T3 yellow, and pJ241

July 29th

J24679+B1002 (B) and (D) were resent to the sequencing center using the R primer.

Digests:

- R0061(ES)
- R0062(ES)
- R0063(ES)
- K091146(ES) 
- K091107(ES)
- pJ241 (XP)
- pSB1T3 yellow (XP)
- K3 (EP)
- T3 (EP)

Grow for tomorrow:

- K145150
- K3 
- R0063
- R0061
- RFP+RBS

Minipreps done today:

-P0451+R0010 B
-R0451+R0010 C
-pSBT13 yellow
-pJ241
-pSBT13 red

Sent to sequencing:

1)pSBT13 red (forward+reverse)
2)pSBT13 yellow (forward+reverse)

Gel:

-Ladder
-pJ241
-pSB1T3 red
-pSB1T3 yellow

-All bands showed up correctly and so all three were cut out and then gel purified.

July 30th

Minipreps done today:

-K145150
-R0063
-K3
-RFP+RBS

Digests:

-Lux+RBS+A3 (XP)
-J23100 (ES+phosphatase)
-J24679+B1002 (XP)
-C0261 (EP+phosphatase)
-RFP+RBS (XP)
-R0062 (EP+phosphatase)
-R0063 (EP+phosphatase)
-K145150 (EP+phosphatase)
-K091107 (EP+phosphatase)
-K091146 (EP+phosphatase)

Ligations:

- Lux+RBS+A3 + J23100 + C3
- J24679+B1002 + C0261 + C3
- RFP+RBS + R0062 + C3
- RFP+RBS + R0063 + C3
- RFP+RBS + K145150 + C3
- RFP+RBS + K091107 + C3
- RFP+RBS + K091146 + C3

Grow for next week:

-R0061
-Electrocompetent cells

August 1st

Colony PCR

1) J23100+Lux+RBS+C3
2) R0062+RFP+RBS+C3 redo
3) K091107+RFP+RBS+C3 redo
4) K091146+RFP+RBS+C3 redo

Return to Notebook

@@ Line 1: / Line 1: @@
+==July 26th==
+*Colony PCR:
+  -J24679+B1002+K3
+  -J24679+B1006+K3
+  -Lux+RBS+B1006+K3 redo
+  -Lux+RBS+B1002+K3
+*Digests:
+  -Lux+RBS (EP)
+  -A3 (EP+Phosphatase)
+*Ligations:
+  -Lux+RBS+A3
+*Gel Order:
+  -Ladder
+  -J24679+B1002+K3 (A-E)
+  -J24679+B1006+K3 (A-E)
 <center>[[Image:7-26-10.jpg]]</center>
+The bands for 1B and 1D showed up so they were grown up accordingly.
+==July 27th==
+*Digests:
+  - C0261 (ES)
+  - R0010 (ES)
+  - J23100(ES)
+  - J24679(XP)
+  - P0451 (XP)
+  - LuxR+RBS (XP)
+*The colony PCR that was done yesterday was ran on a gel. The gel order is as follows:
+ - Ladder
+ - J24679+B1006+K3 (E)
+ - Lux+RBS+B1006+K3 redo (A-E)
+ - Lux+RBS+B1002+K3 (A-E)
 <center>[[Image:7-27-10.jpg]]</center>
+*A second gel was ran from the digests that were done today. The gel order is provided below:
+ -Ladder
+ -pSB1T3 yellow
+ -pJ241
+ -A-E
 <center>[[Image:7-27-10 001.jpg]]</center>
+*Items sent to sequencing:
+*Sent to sequencing:
+) J24679+B1002 B (Reverse)
+) J24679+B1002 D (Reverse)
+) LuxR+RBS+A3 C (Forward+Reverse)
+) LuxR+RBS+A3 A (Forward+Reverse)
+*Grow for tomorrow:
+ -C0261
+ -J23100
+ -pJ241
+ -pSB1T3 yellow
+All 3 pigments were streaked onto the plate to make new stocks.
+*Only pJ241 was ligated because there was a top and bottom band and we were not sure which was the actual pigment we extracted.
+==July 28th==
+Colony PCR Gel:
+ - Ladder
+ -13A-E
+ -14A-D
+: P0451+R0010
+: J23100+LuxR+RBS
 <center>[[Image:7-28-10.jpg]]</center>
+*Since 13B and C grew, we sent those to sequencing with forward and reverse primers. Lux+RBS+A3 was also sent to sequencing with the same primers.
+*We also grew up pSB1T3 red, pSB1T3 yellow, and pJ241
+==July 29th==
+*J24679+B1002 (B) and (D) were resent to the sequencing center using the R primer.
+*Digests:
+ - R0061(ES)
+ - R0062(ES)
+ - R0063(ES)
+ - K091146(ES)
+ - K091107(ES)
+ - pJ241 (XP)
+ - pSB1T3 yellow (XP)
+ - K3 (EP)
+ - T3 (EP)
+*Grow for tomorrow:
+ - K145150
+ - K3
+ - R0063
+ - R0061
+ - RFP+RBS
+*Minipreps done today:
+ -P0451+R0010 B
+ -R0451+R0010 C
+ -pSBT13 yellow
+ -pJ241
+ -pSBT13 red
+*Sent to sequencing:
+)pSBT13 red (forward+reverse)
+)pSBT13 yellow (forward+reverse)
+*Gel:
+ -Ladder
+ -pJ241
+ -pSB1T3 red
+ -pSB1T3 yellow
+<center>[[Image:7-29-10.jpg]]</center>
+-All bands showed up correctly and so all three were cut out and then gel purified.
+==July 30th==
+*Minipreps done today:
+ -K145150
+ -R0063
+ -K3
+ -RFP+RBS
+*Digests:
+ -Lux+RBS+A3 (XP)
+ -J23100 (ES+phosphatase)
+ -J24679+B1002 (XP)
+ -C0261 (EP+phosphatase)
+ -RFP+RBS (XP)
+ -R0062 (EP+phosphatase)
+ -R0063 (EP+phosphatase)
+ -K145150 (EP+phosphatase)
+ -K091107 (EP+phosphatase)
+ -K091146 (EP+phosphatase)
+*Ligations:
+ - Lux+RBS+A3 + J23100 + C3
+ - J24679+B1002 + C0261 + C3
+ - RFP+RBS + R0062 + C3
+ - RFP+RBS + R0063 + C3
+ - RFP+RBS + K145150 + C3
+ - RFP+RBS + K091107 + C3
+ - RFP+RBS + K091146 + C3
+*Grow for next week:
+ -R0061
+ -Electrocompetent cells
+==August 1st==
+*Colony PCR
+) J23100+Lux+RBS+C3
+) R0062+RFP+RBS+C3 redo
+) K091107+RFP+RBS+C3 redo
+) K091146+RFP+RBS+C3 redo
+[https://2010.igem.org/Team:Penn_State/Notebook Return to Notebook]