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Team:University of Lethbridge/Notebook/GeneralLabJune
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===June 6 2008=== | ===June 6 2008=== | ||
| - | ====Sebastian and Roxanne ==== | + | ====Sebastian, John and Roxanne ==== |
Prepared 1L of semi-solid media following the procedure found on OpenWetWare. | Prepared 1L of semi-solid media following the procedure found on OpenWetWare. | ||
-10g peptone (substituted for tryptone) | -10g peptone (substituted for tryptone) | ||
Revision as of 16:43, 22 June 2008
Contents |
June 6 2008
Sebastian, John and Roxanne
Prepared 1L of semi-solid media following the procedure found on OpenWetWare.
-10g peptone (substituted for tryptone) -10g Agar -10g NaCl -5g Yeast Extract
Stored media in fridge.
June 10 2008
Christa, Munima, Roxanne, and Sebastian
Prepared 1L of liquid media following the procedure found on OpenWetWare.
-10g peptone -10g NaCl -5g Yeast Extract
Poured 36 culture test tubes, and the remainder was left in a 1L Erlenmeyer flask. Stored both in fridge.
Christa
Made an inventory of iGEM 2007 parts in Wieden -80 freezer inventory.xls
Roxanne
Defrosted the -20 freezer in the teaching lab for iGEM use (with a little help from my friends!)
June 11 2008
Sebastian, Munima, Roxanne, Christa
Poured 8 minimal media (labeled control- with blue sharpie) plates and 14 amp plates (labeled amp - with red sharpie) stored in the 4 C fridge. Amp concentration is always 50ug/mL.
June 16 2008
Nathan Puhl, Munima, Christa, Sebastian, Roxanne
Plated cheZ knockout strain from glycerol on LB + amp and Plain LB to assess viability and antibiotic resistance at 37 C overnight.
Transformed supercompotent cells with basic biobrick vector pSB1A7 (ampicillin resistance)
-50 uL of cells, 0.85 uL 2-mercaptoethanol, 1 uL of plasmid dissolved with 15 uL of ddH2O -30 min on ice -45 s at 42 C -2 min on ice -Add 0.9 mL of LB shaker incubate at 225 RPM and 37 C
June 17 2008
Munima, Christa, Nathan Puhl
Checked plates
-cheZ knockout strain viable on Lb, no growth on LB + amp - Good -Only one colony from transformation, not very good efficiency, don't know why because too many possibilities, most likely amount of DNA due to inability to quantifiy plasmid from iGEM plates -Subcultured colony in liquid LB + amp -Plate 200 uL on LB + amp at 37 C overnight
June 18 2008
Munima, Christa, Alix, Nathan Puhl
Made glycerol stock of pSB1A7 transformed E. coli
Extracted plasmid from transformed E. coli using the Eppendorff FastPlasmid minikit and stored 4 aliquots of 25 uL in the -20 C freezer.
June 19 2008
Nathan Puhl, Alix, Munima, Christa, Roxanne
Ran plasmids on 1% agarose gel with High range ladder
