Team:HokkaidoU Japan/Notebook/August26
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- | = | + | =Electrophoresis of pSB1C3 concentrated to 50 ug/uL= |
[[Image:HokkaidoU Japan 20100826a.jpg|200px|right|thumb|Electrophoresis of concentrated pSB1C3]] | [[Image:HokkaidoU Japan 20100826a.jpg|200px|right|thumb|Electrophoresis of concentrated pSB1C3]] | ||
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- | |[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png | + | |[https://2010.igem.org/Image:HokkaidoU_Pictures_DNA_Marker.png λ/''Hin''d III & EcoR I] |
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* Only band visible was monomer(about 2000 bp) | * Only band visible was monomer(about 2000 bp) | ||
- | =pSB1A3, pSB1C3 | + | =Filtration of pSB1A3, pSB1C3 and pSB1K3 PCR solutions= |
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+ | 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)