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| {{Template:HokkaidoU_Japan}}<div class="linkbar"><div class="prev">[[Team:HokkaidoU_Japan/Notebook/September15|September 15]]</div>[[Team:HokkaidoU_Japan/Notebook|Notebook]]<div class="next">[[Team:HokkaidoU_Japan/Notebook/September17|September 17]]</div></div> | | {{Template:HokkaidoU_Japan}}<div class="linkbar"><div class="prev">[[Team:HokkaidoU_Japan/Notebook/September15|September 15]]</div>[[Team:HokkaidoU_Japan/Notebook|Notebook]]<div class="next">[[Team:HokkaidoU_Japan/Notebook/September17|September 17]]</div></div> |
- | == Digestion of GFP and Double Terminator ==
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- | ===Parts Information===
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- | {| class="protocol"
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- | |-
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- | |GFP
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- | |BBa_E0040
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- | |1-14K
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- | |720bp
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- | |pSB1A3
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- | |-
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- | |double terminator
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- | |BBa_B0015
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- | |1-23L
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- | |129bp
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- | |pSB1AK3
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- | |-
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- | |pSB1A3
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- | |pSB1A3
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- | | -
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- | |2157bp
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- | |pSB1A3
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- | |}
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- |
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- | 1-14K and pSB1A3 had purified with mycrocon, and 1-23L had extracted from a gel before.
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- |
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- | * electrophoresed 1ul of 1-14K and 1-23L added 0.5ul of 6×sample buffer to estimate concentration of each solution.
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- | * estimated concentration from photo of electrophoresys.But I forgot to electrophorese pSB1A3 solution with the other samples,so pSB1A3 solution was done by other person.
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- | * made digestion recipes based on each concentrations(below). Why pSB1A3 recipe is two, because I firstly made 30ul of pSB1A3 solution, but I found it was insufficient to ligate parts, so I made more 50ul of it after.
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- |
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- | {|style="text-align:center;" class="protocol"
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- | |-
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- | |1-14K
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- | |200 ng/ul
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- | |-
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- | |1-23L
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- | |120 ng/ul
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- | |-
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- | |pSB1A3
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- | |2.5 ng/ul
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- | |}
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- |
| |
- | ===Digestion Menu===
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- | {|style="text-align:center; float:left;" class="protocol"
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- | |-
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- | |1-23L
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- | |0.5 uL
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- | |-
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- | |10x M buffer
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- | |5 uL
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- | |-
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- | |0.1%BSA
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- | |5 uL
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- | |-
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- | |Xba I
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- | |4 uL
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- | |-
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- | |Pst I
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- | |0.5 uL
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- | |-
| |
- | |DW
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- | |35 uL
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- | |-
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- | |style="border-top:1px solid #000;"|'''Total'''
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- | |style="border-top:1px solid #000;"|'''50 uL'''
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- | |}
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- |
| |
- | {|style="text-align:center; float:left;" class="protocol"
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- | |-
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- | |1-14K
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- | |1.5 uL
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- | |-
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- | |10x H buffer
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- | |2 uL
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- | |-
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- | |0.1% BSA
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- | |2 uL
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- | |-
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- | |EcoR I
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- | |1 uL
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- | |-
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- | |Spe I
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- | |0.5 uL
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- | |-
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- | |DW
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- | |13 uL
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- | |-
| |
- | |style="border-top:1px solid #000;"|'''Total'''
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- | |style="border-top:1px solid #000;"|'''20 uL'''
| |
- | |}
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- |
| |
- | {|style="text-align:center; float:left;" class="protocol"
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- | |-
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- | |pSB1A3
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- | |20 uL
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- | |-
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- | |10x H buffer
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- | |3 uL
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- | |-
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- | |0.1% BSA
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- | |3 uL
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- | |-
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- | |EcoR I
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- | |0.5 uL
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- | |-
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- | |Pst I
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- | |0.5 uL
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- | |-
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- | |DW
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- | |3 uL
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- | |-
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- | |style="border-top:1px solid #000;"|'''Total'''
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- | |style="border-top:1px solid #000;"|'''30 uL'''
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- | |}
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- |
| |
- | {|style="text-align:center; float:left;" class="protocol"
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- | |-
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- | |pSB1A3
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- | |30 uL
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- | |-
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- | |10x H buffer
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- | |5 uL
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- | |-
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- | |0.1% BSA
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- | |5 uL
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- | |-
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- | |EcoR I
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- | |0.5 uL
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- | |-
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- | |Pst I
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- | |0.5 uL
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- | |-
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- | |DW
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- | |9 uL
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- | |-
| |
- | |style="border-top:1px solid #000;"|'''Total'''
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- | |style="border-top:1px solid #000;"|'''30 uL'''
| |
- | |}
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- |
| |
- | <div style="clear:both"></div>
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- |
| |
- | # put each solutions into 37℃ incubator.1-23L solution was put about a half and two hours,1-14K solution was done about a half and an hour,30ul of pSB1A3 solution was done about an hour,and 50ul of pSB1A3 was done about a half hour.
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- |
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- |
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- | # electrophoresed each solutions added 6×sample buffer.put 12uls each into wells of a gel.
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- |
| |
- | {|
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- | |-
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- | |1
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- | |λ/''Hin''dIII, EcoR I
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- | |-
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- | |2~3
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- | |1-14K
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- | |-
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- | |4~8
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- | |1-23L
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- | |-
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- | |9~16
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- | |pSB1A3
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- | |}
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- |
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- |
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- | * cannot see 1-23L because of overflowing.extracted the other samples from a gel.dissolve them with 50ul of Nuclease free water.And they were stocked to freeze in -20℃.
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