Team:Kyoto/Luminescence/Note

From 2011.igem.org

(Difference between revisions)
(Aug 4th, 2011)
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* corn flour 45g
* corn flour 45g
* glucose 50g
* glucose 50g
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* agalose 3.5g
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* agarose 3.5g
* propionic acid 1.5mL
* propionic acid 1.5mL
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|
-
# Stir dry yeast and agalose with about two-thirds of water. Then, autoclave it.
+
# Stir dry yeast and agarose with about two-thirds of water. Then, autoclave it.
# Stir corn flour and glucose with the remaining water.
# Stir corn flour and glucose with the remaining water.
# Stir 1 and 2, then autoclave it again.
# Stir 1 and 2, then autoclave it again.
Line 23: Line 23:
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* We dispensed the standard-medium into 3 bottles.
* We dispensed the standard-medium into 3 bottles.
 +
*Kusaba made a convenient tube for taking flies.
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 +
== Aug 5th, 2011 ==
 +
*When we move flies to bottle No.4, we sadly found most of they drown. Then we wipe off the water drops inside the bottles and use dry heat sterilizer to dry them. The problem is solved and we dispense flies to No.5 and No.6, from No.4 and No.2 respectively.
 +
*An extra 0.3g agarose is added into the 100ml standard-medium to make the solid-medium. We clean the bottle No.4 and dispense the solid-medium into it and labeled No.7.
 +
*We practiced ice anesthesia. 
 +
 +
== Aug 6th, 2011 ==
 +
*After drying lightly the bottle No.7, we move the flies from No.3 into it.
 +
 +
== Aug 7th, 2011 ==
 +
*We dispensed standard-medium to six bottles and solid-medium to another two bottles.
 +
 +
== Aug 8th, 2011 ==
 +
*Not enough flies to dispense.
 +
*The experimental plan was made.
 +
 +
== Aug 9th, 2011 ==
 +
*Move part of the flies from No.6 to No.8(standard-medium).
 +
*Supplement the standard-medium in No.1~3.
 +
== Aug 11th, 2011 ==
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== Aug 12th, 2011 ==
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== Aug 17th, 2011 ==
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== Aug 18th, 2011 ==
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== Aug 19th, 2011 ==
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== Aug 22th, 2011 ==
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== Aug 23th, 2011 ==
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== Aug 24th, 2011 ==
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== Aug 25th, 2011 ==
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== Aug 26th, 2011 ==
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== Aug 27th, 2011 ==
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== Aug 28th, 2011 ==
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== Aug 30th, 2011 ==

Revision as of 05:53, 3 September 2011

This page is the note of Luminescence Group.

Contents

Aug 4th, 2011

  • We got drosophila melanogaster(oregon-rs) in 3 tubes from [http://gcoe.biol.sci.kyoto-u.ac.jp/gcoe/eng/member/2008/07/fuse_naoyuki.php Mr. Fuse].
  • We made [http://www.biol.se.tmu.ac.jp/fly/www/standard-medium.html standard medium of Tokyo Metropolitan Univ. for drosophila].
[http://www.biol.se.tmu.ac.jp/fly/www/standard-medium.html Standard medium of Tokyo Metropolitan Univ. for drosophila]
Materials Methods
  • water 500mL
  • dry yeast 20g
  • corn flour 45g
  • glucose 50g
  • agarose 3.5g
  • propionic acid 1.5mL
  1. Stir dry yeast and agarose with about two-thirds of water. Then, autoclave it.
  2. Stir corn flour and glucose with the remaining water.
  3. Stir 1 and 2, then autoclave it again.
  4. after autoclave, add propionic acid into it.■
  • We dispensed the standard-medium into 3 bottles.
  • Kusaba made a convenient tube for taking flies.

Aug 5th, 2011

  • When we move flies to bottle No.4, we sadly found most of they drown. Then we wipe off the water drops inside the bottles and use dry heat sterilizer to dry them. The problem is solved and we dispense flies to No.5 and No.6, from No.4 and No.2 respectively.
  • An extra 0.3g agarose is added into the 100ml standard-medium to make the solid-medium. We clean the bottle No.4 and dispense the solid-medium into it and labeled No.7.
  • We practiced ice anesthesia.

Aug 6th, 2011

  • After drying lightly the bottle No.7, we move the flies from No.3 into it.

Aug 7th, 2011

  • We dispensed standard-medium to six bottles and solid-medium to another two bottles.

Aug 8th, 2011

  • Not enough flies to dispense.
  • The experimental plan was made.

Aug 9th, 2011

  • Move part of the flies from No.6 to No.8(standard-medium).
  • Supplement the standard-medium in No.1~3.

Aug 11th, 2011

Aug 12th, 2011

Aug 17th, 2011

Aug 18th, 2011

Aug 19th, 2011

Aug 22th, 2011

Aug 23th, 2011

Aug 24th, 2011

Aug 25th, 2011

Aug 26th, 2011

Aug 27th, 2011

Aug 28th, 2011

Aug 30th, 2011