Exeter/10 July 2013

From 2013.igem.org

(Difference between revisions)

Latest revision as of 19:53, 2 October 2013

Exeter iGEM 2013 · Paint by Coli

Morning

- [http://parts.igem.org/Part:BBa_K322122 BBa_K322122] (cyan pigment) comes with the machinery to produce our pigment, albeit in low concentrations. 1 ml of the BBa_K322122 liquid cultures from yesterday were transferred to eppendorf tubes and span down into a pellet at 13000 rpm for 5 minutes. All pellets were white, meaning further investigation is required to produce a colour.

MiniPrep of the following Parts:

- [http://parts.igem.org/Part:BBa_K322122 BBa_K322122], cyan pigment

- [http://parts.igem.org/Part:BBa_K592012 BBa_K592012], magenta pigment

- [http://parts.igem.org/Part:BBa_K592010 BBa_K592010], yellow pigment

Plasmids extracted are now in storage at -20°C.

Afternoon

Liquid cultures of the blue light module and magenta pigment

- [http://parts.igem.org/Part:BBa_K592010 BBa_K592010], yellow pigment

- [http://parts.igem.org/Part:BBa_K592012 BBa_K592012], magenta pigment

- [http://parts.igem.org/Part:BBa_B0015 BBa_B0015], a terminator

- [http://parts.igem.org/Part:BBa_K592005 BBa_K592005], FixJ protein intermediate

- [http://parts.igem.org/Part:BBa_K592004 BBa_K592004], blue light sensor

Retry of BBa_B0034 transformation

Normal transformation protocol from 4/7/13 followed. Made certain we were using the right antibiotic plates!

(Next day, results of [http://parts.igem.org/Part:BBa_B0034 BBa_B0034] transformation)

We made two plates of [http://parts.igem.org/Part:BBa_B0034 BBa_B0034], each plate had 7 colonies. Our RFP control had 137 colonies.

Take me back to the notebook.

Exeter iGEM 2013 · Paint by Coli

@@ Line 1: / Line 1: @@
+{{:Team:Exeter/Template/Header}}
+<div class="container">
+    <div class="row">
+        <div class="span" style="text-align:justify">
 == Morning ==
+- [http://parts.igem.org/Part:BBa_K322122 BBa_K322122] (cyan pigment) comes with the machinery to produce our pigment, albeit in low concentrations. 1 ml of the BBa_K322122 liquid cultures from yesterday were transferred to eppendorf tubes and span down into a pellet at 13000 rpm for 5 minutes. All pellets were white, meaning further investigation is required to produce a colour.
 MiniPrep of the following Parts:
-- BBa_K322122, cyan pigment
+- [http://parts.igem.org/Part:BBa_K322122 BBa_K322122], cyan pigment
-- BBa_K592012, magenta pigment
+- [http://parts.igem.org/Part:BBa_K592012 BBa_K592012], magenta pigment
-- BBa_K592010, yellow pigment
+- [http://parts.igem.org/Part:BBa_K592010 BBa_K592010], yellow pigment
-Plasmids extracted are now in storage at -20oC.
+Plasmids extracted are now in storage at -20&deg;C.
+==Afternoon==
-=Afternoon=
 '''Liquid cultures of the blue light module and magenta pigment'''
-- BBa_K592010, yellow pigment
+- [http://parts.igem.org/Part:BBa_K592010 BBa_K592010], yellow pigment
-- BBa_K592012, magenta pigment
+- [http://parts.igem.org/Part:BBa_K592012 BBa_K592012], magenta pigment
-- BBa_B0015, a terminator
+- [http://parts.igem.org/Part:BBa_B0015 BBa_B0015], a terminator
-- BBa_K592005, FixJ protein intermediate
+- [http://parts.igem.org/Part:BBa_K592005 BBa_K592005], FixJ protein intermediate
-- BBa_K592004, blue light sensor
+- [http://parts.igem.org/Part:BBa_K592004 BBa_K592004], blue light sensor
 '''Retry of BBa_B0034 transformation'''
@@ Line 31: / Line 35: @@
 Normal transformation protocol from 4/7/13 followed. Made certain we were using the right antibiotic plates!
-=(Next day, results of BBa_B0034 transformation)=
+==(Next day, results of [http://parts.igem.org/Part:BBa_B0034 BBa_B0034] transformation)==
+We made two plates of [http://parts.igem.org/Part:BBa_B0034 BBa_B0034], each plate had 7 colonies. Our RFP control had 137 colonies.
+Take me back to the [https://2013.igem.org/Team:Exeter/Notebook notebook].
-We made two plates of BBa_B0034, each plate had 7 colonies. Our RFP control had 137 colonies.
+   </div>
+</div>
+{{:Team:Exeter/Template/Footer}}