Valencia/October

From 2007.igem.org

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===3/10/07===
===3/10/07===
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we have digested the plasmid were we did the PCRs with EcoRI and PstI
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we have digested the plasmid that were amplified with the PCRs with ''Eco''RI and ''Pst''I, because we want to be sure if it is, or if it is not, what we want... at the gel we see two bands on one clone and three (??) on the other... and the weights are not the correct ones... we must have had some false positives clones...
 +
 
 +
we prepare more inoculations to ligate tomorrow...
 +
 
 +
===4/10/07===
 +
 
 +
we are miniprepping and digesting the comparator device with the fluorescences... let's see if you can transform this evening...
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===<div align="right">[[Valencia/November|November &rarr;]]</div>===
===<div align="right">[[Valencia/November|November &rarr;]]</div>===

Revision as of 11:50, 4 October 2007

Work Progress

July
Mo Tu We Th Fr Sa Su
26 27  28 29 30 31  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   1  2  3  4  5
August
Mo Tu We Th Fr Sa Su
30 31   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  1  2
September
Mo Tu We Th Fr Sa Su
27 28  29 30 31  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
October
Mo Tu We Th Fr Sa Su
 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  1  2  3  4
November
Mo Tu We Th Fr Sa Su
29 30  31  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  1  2

← September

1/10/07

we leave some overnight PCRs reactions, using VF2 and VR, in order to properly analyze our clones...

at the same time, we are inoculating all those clones in order to make some minipreps.

2/10/07

we have done the gel of the PCR reactions, but it looks like the DNA has not amplified our samples, but the reaction has worked fine for the controls.

we repeat the PCRs and make some other controls with different DNA quantities. the gels shows some bands, but their weights do not correspond to anything we wanted... could be some other lab dwarf??

we have miniprepped the inoculations that have grown overnight. this way, we will have more DNA to sequence

3/10/07

we have digested the plasmid that were amplified with the PCRs with EcoRI and PstI, because we want to be sure if it is, or if it is not, what we want... at the gel we see two bands on one clone and three (??) on the other... and the weights are not the correct ones... we must have had some false positives clones...

we prepare more inoculations to ligate tomorrow...

4/10/07

we are miniprepping and digesting the comparator device with the fluorescences... let's see if you can transform this evening...