Team:Glendale CC AZ/igem.org

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(Created page with "'''Purpose''': To isolate the plasmid DNA from transformed cells. '''Reagents''': *Lysis solution (50mM glucose, 25mM TrisHCl pH 8, 10 mM EDTA) : 9.0mL dH2O : 0.25mL 1M T...")
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'''Purpose''': To isolate the plasmid DNA from transformed cells.
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{{:Team:Glendale_CC_AZ/test}}
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'''Reagents''':  
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*Lysis solution (50mM glucose, 25mM TrisHCl pH 8, 10 mM EDTA)
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: 9.0mL dH2O
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: 0.25mL 1M TrisHCl pH 8
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: 0.25mL 0.5 M Na2EDTA
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: 0.50mL 20% glucose
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*SDS/NaOH (prepare fresh)
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:880ul dH2O
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:100ul 10% SDS
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:20ul 10M NaOh
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*Acetate solution
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:60mL 5M potassium acetate
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:11.5mL glacial acetic acid
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:28.5mL dH2O
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'''Materials''':
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-1 colony of transformed cells
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-5mL LB/chloramphenicol media
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-Microcentrifuge
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-Microcentrifuge tubes
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-Micropipette
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-Disposable tips
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-200ul lysis solution
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-400ul SDS/NaOH (made fresh)
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-300ul acetate solution
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-1000ul isopropanol
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-400ul 70% ethanol
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-Kimwipes
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-100ul TE
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Procedure:
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# Inoculate 5ml of LB/antibiotic (chloramphenicol) with a single colony of transformed cells. Incubate overnight at 37ºC with shaking.
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# Optionala: Keep 2mL of the bacterial culture for indexing. Pipet 1.5mL of culture into a microcentrifuge tube, and microcentrifuge at 10,000 rpm for 1 minute. Discard the supernatant, and add the remaining 1.5mL of culture to the same microcentrifuge tube. Centrifuge the tube for 1 more minute at 10,000 rpm and discard supernatant one more time.
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# Resuspend the pellet in 200ul of lysis solution. Incubate at room temperature for 5 minutes.
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# Add 400ul of SDS/NaOH (made fresh) and invert 3-6 times. Incubate on ice for 5 minutes, solution will become clear and viscous.
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# Add 300ul of acetate solution, gently mix for a few seconds, and incubate on ice for 10 minutes.
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# Centrifuge for 3 minutes at 10,000 rpm in microcentrifuge.
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# Decant supernatant into a clean microcentrifuge tube; avoid the loose, viscous pellet.
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# Add 1 volume of isopropanol and invert tube 3-6 times. Incubate at room temperature for 10 minutes to precipitate DNA.
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# Centrifuge at 10,000 rpm for 10 minutes. Orient hinge to the same direction in case pellet is hard to see.
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# Discard supernatant, removing residual liquid with pipet tip. Add 200-400ul 70% ethanol, agitate pellet gently and centrifuge at 10,000 rpm for 10 min to precipitate pellet.
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# Discard supernatant, being careful to avoid losing the pellet. Let rest at room temperature with the lid open or inverted on a Kimwipe to evaporate residual alcohol.
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# Dissolve pellet in just enough TE to dissolve the DNA, approx. 50-55ul. Optional: Let pellet hydrate overnight.
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Latest revision as of 23:39, 31 July 2013

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