Team:HokkaidoU Japan/Notebook/August26
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- | = | + | <div class="linkbar"><div class="prev">[[Team:HokkaidoU_Japan/Notebook/August25|August 25]]</div>[[Team:HokkaidoU_Japan/Notebook|Notebook]]<div class="next">[[Team:HokkaidoU_Japan/Notebook/August27|August 27]]</div></div> |
- | [[Image:HokkaidoU Japan 20100826a.jpg|200px|right|thumb|]] | + | |
- | * | + | =Electrophoresis of pSB1C3 concentrated to 50 ug/uL= |
- | {| | + | |
+ | [[Image:HokkaidoU Japan 20100826a.jpg|200px|right|thumb|Electrophoresis of concentrated pSB1C3]] | ||
+ | |||
+ | * Added 2.8 uL of 6x SB to 17.4 uL of pSB1C3 solution digested yesterday and electrophoresed | ||
+ | |||
+ | {| class="protocol" | ||
|- | |- | ||
- | | | + | |'''Lane''' |
- | | | + | |'''DNA''' |
|- | |- | ||
|1 | |1 | ||
- | | | + | |Added too much of marker, mistake |
|- | |- | ||
|2 | |2 | ||
- | |λ/''Hin''d III & EcoR I | + | |[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png λ/''Hin''d III & EcoR I] |
|- | |- | ||
|3 | |3 | ||
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|} | |} | ||
- | * | + | * IF digestion and ligation went well there should be bands of dimers, trimers but none of the were visible |
- | * | + | * Only band visible was monomer(about 2000 bp) |
+ | |||
+ | =Filtration of pSB1A3, pSB1C3 and pSB1K3 PCR solutions= | ||
- | + | Remaining amount from check via electrophoresis,namely 49 uL was filtrated with Microcon YM-10 | |
- | + |
Latest revision as of 07:54, 27 October 2010
Electrophoresis of pSB1C3 concentrated to 50 ug/uL
- Added 2.8 uL of 6x SB to 17.4 uL of pSB1C3 solution digested yesterday and electrophoresed
Lane | DNA |
1 | Added too much of marker, mistake |
2 | λ/Hind III & EcoR I |
3 | pSB1C3 solution |
4 | pSB1C3 solution |
- IF digestion and ligation went well there should be bands of dimers, trimers but none of the were visible
- Only band visible was monomer(about 2000 bp)