Team:KULeuven/28 August 2008

From 2008.igem.org

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== Lab Work ==
== Lab Work ==
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[[image:gel-28-8a.jpg|right|thumb|350px|'''Gel 1''': Test ligation with PCR. All 4 colonies of K145151+pSB1A2 ligated properly, but only the first colony of K145001+pSB1A2 ligated properly]]
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[[image:gel-28-8b.jpg|right|thumb|350px|'''Gel 2''': Digests of B0015, C0012, C0060, K145015 and C0040]]
=== Wet Lab ===
=== Wet Lab ===
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* The ligations with B0015 (C0012+B0015, C0060+B0015, C0040+B0015, K145001+B0015, K145151+B0015, K45015+B0015) were electroporated again, but now they were plated on an ampicillin plate.  
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The ligations with B0015 ([http://partsregistry.org/Part:BBa_C0040 C0040]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_C0060 C0060]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_C0012 C0012]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145015 K145015]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145001 K145001]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145151 K145151]+[http://partsregistry.org/Part:BBa_B0015 B0015]) were electroporated again, but now they were plated on an ampicillin plate.  
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* A glycerol stock was made of the succeeded ligations.
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* The new parts arrived today. They were also plated.  
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A glycerol stock was made of the succeeded ligations.
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* The ligations of K145001 and K145151 with pSB1A2 were MiniPrepped and then we did a PCR to test the ligation.
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* The digests of R0011, R0040+J23022, C0062 and B0033 were put on gel and purified.
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We ordered some new parts, because the modeling showed that a lot of things had to be changed. They arrived today and they were also plated.  
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* Some more digests were made, but this time we cut with ''Spe''I, ''Xba''I and ''Pst''I. We cut B0015 as insert and C0060, K145015, C0012 and C0040 were cut as vector.
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The ligations of [http://partsregistry.org/Part:BBa_K145001 K145001] and [http://partsregistry.org/Part:BBa_K145151 K145151] with [http://partsregistry.org/Part:pSB1A2 pSB1A2] were miniprepped and then we did a PCR to test the ligation (primers VF/VR-2). See '''Gel 1'''.
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The digests of [http://partsregistry.org/Part:BBa_R0011 R0011], [http://partsregistry.org/Part:BBa_R0040 R0040]+[http://partsregistry.org/Part:BBa_J23022 J23022], [http://partsregistry.org/Part:BBa_C0062 C0062] and [http://partsregistry.org/Part:BBa_B0033 B0033] were put on gel and purified.
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Some more digests were made, but this time we cut with ''Spe''I, ''Xba''I and ''Pst''I. We cut [http://partsregistry.org/Part:BBa_B0015 B0015] as insert (''Xba''I and ''Pst''I) and [http://partsregistry.org/Part:BBa_C0060 C0060], [http://partsregistry.org/Part:BBa_K145015 K145015], [http://partsregistry.org/Part:BBa_C0012 C0012] and [http://partsregistry.org/Part:BBa_C0040 C0040] were cut as vector (''Spe''I and ''Pst''I). See '''Gel 2'''.
=== Dry Lab ===
=== Dry Lab ===
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==== Ethics ====
We did some more research on bioethics and human practice.  
We did some more research on bioethics and human practice.  
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Simulations of the different parts has continued.
Simulations of the different parts has continued.
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==== Wiki ====
 
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== Remarks ==
 
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{{:Team:KULeuven/Tools/New_Day/Date_Retriever}}
 

Latest revision as of 12:18, 12 October 2008

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Contents

Lab Work

Gel 1: Test ligation with PCR. All 4 colonies of K145151+pSB1A2 ligated properly, but only the first colony of K145001+pSB1A2 ligated properly
Gel 2: Digests of B0015, C0012, C0060, K145015 and C0040

Wet Lab

The ligations with B0015 ([http://partsregistry.org/Part:BBa_C0040 C0040]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_C0060 C0060]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_C0012 C0012]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145015 K145015]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145001 K145001]+[http://partsregistry.org/Part:BBa_B0015 B0015], [http://partsregistry.org/Part:BBa_K145151 K145151]+[http://partsregistry.org/Part:BBa_B0015 B0015]) were electroporated again, but now they were plated on an ampicillin plate.

A glycerol stock was made of the succeeded ligations.

We ordered some new parts, because the modeling showed that a lot of things had to be changed. They arrived today and they were also plated.

The ligations of [http://partsregistry.org/Part:BBa_K145001 K145001] and [http://partsregistry.org/Part:BBa_K145151 K145151] with [http://partsregistry.org/Part:pSB1A2 pSB1A2] were miniprepped and then we did a PCR to test the ligation (primers VF/VR-2). See Gel 1.

The digests of [http://partsregistry.org/Part:BBa_R0011 R0011], [http://partsregistry.org/Part:BBa_R0040 R0040]+[http://partsregistry.org/Part:BBa_J23022 J23022], [http://partsregistry.org/Part:BBa_C0062 C0062] and [http://partsregistry.org/Part:BBa_B0033 B0033] were put on gel and purified.

Some more digests were made, but this time we cut with SpeI, XbaI and PstI. We cut [http://partsregistry.org/Part:BBa_B0015 B0015] as insert (XbaI and PstI) and [http://partsregistry.org/Part:BBa_C0060 C0060], [http://partsregistry.org/Part:BBa_K145015 K145015], [http://partsregistry.org/Part:BBa_C0012 C0012] and [http://partsregistry.org/Part:BBa_C0040 C0040] were cut as vector (SpeI and PstI). See Gel 2.

Dry Lab

Ethics

We did some more research on bioethics and human practice.

Modeling

Great Succes: we succeeded in modeling cell-multiplication in a Matlab-environment. This will be our starting point for modeling cell division and work in a multi-cell environment! [we did what the lab couldn't do]

Parameter checking has almost reached its final state.

Simulations of the different parts has continued.