Team:UNIPV-Pavia/Calendar/August/settimana2

From 2010.igem.org

(Difference between revisions)

Revision as of 18:54, 9 August 2010

AUGUST: WEEK 2

August, 9th

Phasins plates showed very few colonies (12 for I20-new and 17 for I21-new): they were all picked and let grow in LB+Amp 100ug/ml. In the evening we made glycerol stocks and re-filled the tubes for the screening of the following day:

I20-new:

I21-1

I21-2

I21-3

I21-4

I21-5

I21-6

I21-7

I21-8

I21-9

I21-10

I21-11

I21-12

I21-new:

I20-1

I20-2

I20-3

I20-4

I20-5

I20-6

I20-7

I20-8

I20-9

I20-10

I20-11

I20-12

I20-13

I20-14

I20-15

I20-16

I20-17

In order not to loose our time we decided to perform again the PCR-amplification/modification of <partinfo>BBa_K208001</partinfo> in case of a negative screening.

Check of LB+Cm 6 ug/ml agar plates. We let grow at 30°C:

MG1655 in LB
MC1061 in LB
MG123/008 in LB+Amp 50 ug/ml
MC123/008 in LB+Amp 50 ug/ml

Than we streaked cultures on a four-sector divided plate. Since 6 ug/ml is a very low concentration, we wanted to check if actually nothing (without the right resistance) grow on these plates.

Transformation of 100 ul of MG008 and MC123 competent cell to check their efficiency. We used 1 ul (~4 ng) of RING, F2620-4C5, Nothing (water) and plated on proper LB agar plates:

@@ Line 31: / Line 31: @@
 <html><p align="center"><font size="4"><b>AUGUST: WEEK 2</b></font></p></html><hr><br>
 ==August, 9th==
-Phasins plates showed very few colonies (17 for I20-new and 12 for I21-new): they were all picked and let grow in LB+Amp 100ug/ml. In the evening we made glycerol stocks and re-filled the tubes for the screening of the following day:
+Phasins plates showed very few colonies (12 for I20-new and 17 for I21-new): they were all picked and let grow in LB+Amp 100ug/ml. In the evening we made glycerol stocks and re-filled the tubes for the screening of the following day:
 {|border="1" align="center"
-|'''I20-new:'''||I20-1||I20-2||I20-3||I20-4||I20-5||I20-6||I20-7||I20-8||I20-9||I20-10||I20-11||I20-12||I20-13||I20-14||I20-15||I20-16||I20-17
+|'''I20-new:'''||I21-1||I21-2||I21-3||I21-4||I21-5||I21-6||I21-7||I21-8||I21-9||I21-10||I21-11||I21-12
 |-
-|'''I21-new:'''||I21-1||I21-2||I21-3||I21-4||I21-5||I21-6||I21-7||I21-8||I21-9||I21-10||I21-11||I21-12
+|'''I21-new:'''||I20-1||I20-2||I20-3||I20-4||I20-5||I20-6||I20-7||I20-8||I20-9||I20-10||I20-11||I20-12||I20-13||I20-14||I20-15||I20-16||I20-17
 |}
 In order not to loose our time we decided to perform again the PCR-amplification/modification of <partinfo>BBa_K208001</partinfo> in case of a negative screening.
@@ Line 45: / Line 45: @@
 *MG123/008 in LB+Amp 50 ug/ml
 *MC123/008 in LB+Amp 50 ug/ml
-Than we streaked cultures on plates. Since 6 ug/ml is a very low concentration, we wanted to check if actually nothing (without the right resistance) grow on these plates.
+Than we streaked cultures on a four-sector divided plate. Since 6 ug/ml is a very low concentration, we wanted to check if actually nothing (without the right resistance) grow on these plates.
+----
+Transformation of 100 ul of MG008 and MC123 competent cell to check their efficiency. We used 1 ul (~4 ng) of RING, F2620-4C5, Nothing (water) and plated on proper LB agar plates:
+*RING: Cm 34 ug/ml
+*F2620-4C5: Cm 12,5 ug/ml
+*Nothing: Cm 12,5 ug/ml
 ==August, 10th==

Team:UNIPV-Pavia/Calendar/August/settimana2

From 2010.igem.org

Revision as of 18:54, 9 August 2010

August, 9th

August, 10th

August, 11th

August, 12th

August, 13th

August, 14th

August, 15th