Team:Kyoto/Calendar/24 July 2009

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=='''Lab-note on 24 July 2009'''==
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{|
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|Date||'''090724'''||Experimenter||'''Kashima, Takashima, Hibino, Miyazawa'''
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|-
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| || ||Note-taker||'''Takashima'''
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|}
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====Title====
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{|
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|'''7/24 Miniprep Kit, Restriction Enzyme Digestion Electrophoresis'''
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|}
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====Flow Chart====
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{|
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|
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#Miniprep Kit
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#Restriction Enzyme Digestion
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#Electrophoresis
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|}
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{|
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!Sample Date!!Sample Name!!Enzyme!!purification Kit!!Product!!Storage
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|-
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|iGEM DNA parts kit||3-O-2||Eco R1|| || ||6F freezer
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|-
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|iGEM DNA parts kit||3-A-4||Eco R1|| || ||6F freezer
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|-
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|iGEM DNA parts kit||3-O-2||Eco R1<br>PST1|| || ||6F freezer
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|-
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|iGEM DNA parts kit||3-A-4||Eco R1<br>PST1|| || ||6F freezer
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|}
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====Miniprep kit====
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{|
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|
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[3-O-2, 3-A-4]
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#Cultured sample (090722 9:30 ～ 090723 16:50)
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#Centrifuged 2mins at 15000g 4℃.
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#Removed the top of layer.
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#Centrifuged 2mins at 15000g 4℃.
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#Removed the top of layer.
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#Centrifuged 10mins at 14000g 4℃.
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#Applied  the top of layer to column.
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#Centrifuged RT, 10sec and remove through.
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#Added Buffer PB 500µl.
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#Centrifuged RT, 10sec and remove through.
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#Added Buffer PE 650µl.
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#Centrifuged RT, 10sec and remove through.
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#Centrifuged 1min at 17900g 4℃.
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#Exchanged tube. (remove Ethanol)
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#Added Milli Q 50µl RT 1min.
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#Centrifuged 1min at 17900g 4℃.
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#Collected through and measured concentration.
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----
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'''Results'''
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{|
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!Sample!!conc./(ng/µl)
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|-
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|3-O-2||283.5
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|-
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|3-A-4||103.9
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|}
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|}
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====Description (Electropgoresis)====
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{|
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|
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*Gel:'''Agarose'''
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*Time:'''12:50-13:20'''
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*Voltage:'''100 V'''
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{|
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! !!1!!2!!3!!4
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|-
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!Sample
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|3-O-2 (3 µl)||3-A-4 (3 µl)||3-O-2 (3 µl)||3-A-4 (3 µl)
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|-
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!enzyme
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|Eco R1 (0.17 µl)||Eco R1 (0.17 µl)||Eco R1 (0.17 µl)||Eco R1 (0.17 µl)
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|-
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!enzyme
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|PST1 (0.3 µl)||PST1 (0.3 µl)|| ||
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|-
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!Water
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|1 µl||1 µl||1.4 µl||1.4 µl
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|-
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!H buffer
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|8.2 µl||8.2 µl||8.1 µl||8.1µl
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|-
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!Total
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!12.7 µl!!12.7 µl!!12.9 µl!!12.9 µl
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|}
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Revision as of 08:27, 4 August 2009



Contents

Lab-note on 24 July 2009

Date090724ExperimenterKashima, Takashima, Hibino, Miyazawa
Note-takerTakashima

Title

7/24 Miniprep Kit, Restriction Enzyme Digestion Electrophoresis

Flow Chart

  1. Miniprep Kit
  2. Restriction Enzyme Digestion
  3. Electrophoresis
Sample DateSample NameEnzymepurification KitProductStorage
iGEM DNA parts kit3-O-2Eco R1 6F freezer
iGEM DNA parts kit3-A-4Eco R1 6F freezer
iGEM DNA parts kit3-O-2Eco R1
PST1		 6F freezer
iGEM DNA parts kit3-A-4Eco R1
PST1		 6F freezer

Miniprep kit

[3-O-2, 3-A-4]

  1. Cultured sample (090722 9:30 ～ 090723 16:50)
  2. Centrifuged 2mins at 15000g 4℃.
  3. Removed the top of layer.
  4. Centrifuged 2mins at 15000g 4℃.
  5. Removed the top of layer.
  6. Centrifuged 10mins at 14000g 4℃.
  7. Applied the top of layer to column.
  8. Centrifuged RT, 10sec and remove through.
  9. Added Buffer PB 500µl.
  10. Centrifuged RT, 10sec and remove through.
  11. Added Buffer PE 650µl.
  12. Centrifuged RT, 10sec and remove through.
  13. Centrifuged 1min at 17900g 4℃.
  14. Exchanged tube. (remove Ethanol)
  15. Added Milli Q 50µl RT 1min.
  16. Centrifuged 1min at 17900g 4℃.
  17. Collected through and measured concentration.

Results

Sampleconc./(ng/µl)
3-O-2283.5
3-A-4103.9

Description (Electropgoresis)

  • Gel:Agarose
  • Time:12:50-13:20
  • Voltage:100 V
1234
Sample 3-O-2 (3 µl)3-A-4 (3 µl)3-O-2 (3 µl)3-A-4 (3 µl)
enzyme Eco R1 (0.17 µl)Eco R1 (0.17 µl)Eco R1 (0.17 µl)Eco R1 (0.17 µl)
enzyme PST1 (0.3 µl)PST1 (0.3 µl)
Water 1 µl1 µl1.4 µl1.4 µl
H buffer 8.2 µl8.2 µl8.1 µl8.1µl
Total 12.7 µl12.7 µl12.9 µl12.9 µl



Retrieved from "http://2009.igem.org/Team:Kyoto/Calendar/24_July_2009"