Team:Kyoto/Luminescence/Note

From 2011.igem.org

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== Aug 5th, 2011 ==
== Aug 5th, 2011 ==
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*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.
+
*When we transfer 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.
*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.   
*We practiced ice anesthesia.   
== Aug 6th, 2011 ==
== Aug 6th, 2011 ==
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*After drying lightly the bottle No.7, we move the flies from No.3 into it.
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*After drying lightly the bottle No.7, we transfer the flies from No.3 into it.
== Aug 7th, 2011 ==
== Aug 7th, 2011 ==
Line 38: Line 38:
== Aug 8th, 2011 ==
== Aug 8th, 2011 ==
*Not enough flies to dispense.
*Not enough flies to dispense.
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*The experimental plan was made.
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*The experimental plan was made by Kusaba.
   
   
== Aug 9th, 2011 ==
== Aug 9th, 2011 ==
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*Move part of the flies from No.6 to No.8(standard-medium).
+
*Transfer part of the flies from No.6 to No.8(standard-medium).
*Supplement the standard-medium in No.1~3.
*Supplement the standard-medium in No.1~3.
 +
== Aug 11th, 2011 ==
== Aug 11th, 2011 ==
 +
*Transfer flies from No.5 to No.9(standard-medium).
 +
== Aug 12th, 2011 ==
== Aug 12th, 2011 ==
 +
*Transfer the rest of the flies from No.6 to No.10(standard-medium).
 +
== Aug 17th, 2011 ==
== Aug 17th, 2011 ==
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*We transfer the second generation of flies as follows:
 +
**No.1 -> No.11
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**No.2 -> No.12
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**No.3 -> No.13
 +
**No.5 -> No.14
 +
**No.6 -> No.15
 +
*We dispose the imaginal flies of No.7.
 +
== Aug 18th, 2011 ==
== Aug 18th, 2011 ==
 +
*Our group assembled the first experimental system to research the phototaxis of flies. However, the response of flies was not clear and we could not get respectable results.
 +
*Fly dispension:
 +
**No.12 -> No.14
 +
**No.3, 5, 6, 7 -> No.16
 +
**No.1, 2 -> No.17
 +
*We made the medium with a little change as follows:
 +
** agarose 3.5g -> 4.0g
 +
** Add "Bokinin" 5 ml(p-Hydroxybenzoate 0.5 g in 5 ml of 70% alcohol solution)
 +
== Aug 19th, 2011 ==
== Aug 19th, 2011 ==
 +
*Fly dispension:
 +
**No.11 -> No.18(second generation).
 +
**No.5, 6, 7 ->No.19
 +
**No.2, 3 ->No.20
 +
**No.1 -> refrigerator
 +
**No.8 -> No.9
 +
== Aug 22th, 2011 ==
== 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 ==
 

Latest revision as of 07:41, 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 transfer 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 transfer 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 by Kusaba.

Aug 9th, 2011

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

Aug 11th, 2011

  • Transfer flies from No.5 to No.9(standard-medium).

Aug 12th, 2011

  • Transfer the rest of the flies from No.6 to No.10(standard-medium).

Aug 17th, 2011

  • We transfer the second generation of flies as follows:
    • No.1 -> No.11
    • No.2 -> No.12
    • No.3 -> No.13
    • No.5 -> No.14
    • No.6 -> No.15
  • We dispose the imaginal flies of No.7.

Aug 18th, 2011

  • Our group assembled the first experimental system to research the phototaxis of flies. However, the response of flies was not clear and we could not get respectable results.
  • Fly dispension:
    • No.12 -> No.14
    • No.3, 5, 6, 7 -> No.16
    • No.1, 2 -> No.17
  • We made the medium with a little change as follows:
    • agarose 3.5g -> 4.0g
    • Add "Bokinin" 5 ml(p-Hydroxybenzoate 0.5 g in 5 ml of 70% alcohol solution)

Aug 19th, 2011

  • Fly dispension:
    • No.11 -> No.18(second generation).
    • No.5, 6, 7 ->No.19
    • No.2, 3 ->No.20
    • No.1 -> refrigerator
    • No.8 -> No.9

Aug 22th, 2011

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