Difference between revisions of "Team:Aachen/Composite Part"
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{{Team:Aachen/Figure|Aachen_glgCAB for registry.png|title=SDS-PAGE of ''glgCAB'' in pSB1A30|subtitle=''glgCAB'' in pSB1A30 was expressed in Bl21 Gold (DE3) strains and IPTG induced. The small arrows indicates the expected bands for all three enzymes . The Bl21 Gold (DE3) wild type was used as the negative control.|size=large}} | {{Team:Aachen/Figure|Aachen_glgCAB for registry.png|title=SDS-PAGE of ''glgCAB'' in pSB1A30|subtitle=''glgCAB'' in pSB1A30 was expressed in Bl21 Gold (DE3) strains and IPTG induced. The small arrows indicates the expected bands for all three enzymes . The Bl21 Gold (DE3) wild type was used as the negative control.|size=large}} | ||
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+ | The combined functionality was characterized by iodine staining (see picture below). It was performed with Lugol's iodine which dyes glycogen in a brownish color. If more glycogen is present, the color of stainend cultures is darker. The darker staining of Bl21 Gold (DE3) transformants of BBa_K1585321 picture indicates considerably more glycogen accumulations compared to the wild type. | ||
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+ | {{Team:Aachen/Figure|Aachen_glgCAB , WT_v2.png|title=Iodine staining BL21 Gold (DE3) + ''glgCAB'' vs. wild type |subtitle=Cultivated in LB + 20 mM glucose, BL21 Gold (DE3) + ''glgCAB'' stained distinctly darker than the BL21 Gold (DE3) wild type.|size=medium}} | ||
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{{Team:Aachen/Footer|color=green}} | {{Team:Aachen/Footer|color=green}} |
Revision as of 13:29, 18 September 2015