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Revision as of 00:35, 13 September 2015

iGEM Bielefeld 2015


Media & Buffers

All of our favorite recipes.

Media

LB

  • For 1 liter LB:
    • 20 g LB powder
    • Fill the bottle with deionized H2O

  • For 1 L LB-plates:
    • 18 g LB powder
    • 16 g Select Agar
    • Fill the bottle with deionized H2O

SOC

  • Add the following components for 900 mL of distilled H2O:
    • 20 g Trypton
    • 5 g Bacto Yeast Extract
    • 2 mL of 5 M NaCl
    • 2.5 mL of 1 M KCl
    • 10 mL of 1 M MgCl2
    • 10 mL of 1 M MgSO4
    • 20 mL of 1 M glucose
  • For 1 L, combine
    • 16 g tryptone
    • 10 g yeast extract
    • 5 g NaCl
    • 22 mL KH2PO4
    • 40 mL K2HPO4
  • dissolve in water and titrate to pH = 7.0 with NaOH, autoclave

Buffers

  • For each litre of solution:
    • 242 g Tris Base (MW=121.1)
    • 57.1 ml Glacial Acetic Acid
    • 100 ml 0.5 M EDTA

  • mix Tris with stir bar to dissolve in about 600 ml of ddH2O.
  • add the EDTA and Acetic Acid.
  • bring final volume to 1 l with ddH20.
  • store at room temperature.

  • Note: Final (1x) working concentration:
    • 0.04 M Tris - Acetate
    • 0.001 M EDTA
  • For each 200 ml of solution:
    • 5.844 g NaCl
    • 0.272 g imidazole
    • 5.8 ml of 86 % glycerol
    • 0.406 g MgCl2
    • 0.2 g lysozyme

  • Add all these ingredients to a 50 mM sodium phosphate buffer (pH 8.0). Prior to use add DTT to a final concentration of 1mM and tween 20 to a final concentration of 0.1 %.
  • store at room temperature.

  • Note: Final (1x) working concentration:
    • 50 mM Sodiumphosphate
    • 500 mM NaCl
    • 20 mM imidazole
    • 2.5 % glxcerol
    • 1 mM DTT
    • 10 mM MgCl2
    • 0.1 % tween 20
    • 1 mg/ml lysozyme
  • For each litre of solution:
    • 29.22g NaCl
    • 1.36 g imidazole
    • 29 ml of 86 % glycerol

  • Add all these ingredients to a 50 mM sodium phosphate buffer (pH 8.0). Prior to use add DTT to a final concentration of 1mM.
  • store at room temperature.

  • Note: Final (1x) working concentration:
    • 50 mM sodium phosphate
    • 500 mM NaCl
    • 20 mM imidazole
    • 2.5 % glycerol
    • 1 mM DTT
  • For each litre of solution:
    • 17.53 g NaCl
    • 13.6 g imidazole

  • Add all these ingredients to a 20 mM sodium phosphate buffer (pH 7.4).
  • store at room temperature.

  • Note: Final (1x) working concentration:
    • 20 mM sodium phosphate
    • 300 mM NaCl
    • 200 mM imidazole
  • For each litre of solution:
    • 50 g glucose

  • Add the glucose to a 200 mM potassium phosphate buffer (pH 7.6). Prior to usage add DTT to a final concentration of 1 mM
  • store at room temperature.

  • Note: Final (1x) working concentration:
    • 200 mM potassium phosphate
    • 5 % glucose
    • 1 mM DTT
  • 10 mM TRIS-HCl
  • Adjust pH 8 with hydrogen chloride.
  • Add 1 mM DTT to the buffer.
  • Add KCl or NaCl as needed.
  • For the optimal binding buffer 500 mM KCl is added.
  • 50 mM HEPES
  • Adjust pH 7.2 with hydrogen chloride.
  • 20 mM Na2HPO4, pH 8
  • 100 mM sodium phosphate buffer, pH 8.0
  • 375 mM KCl
  • 25% glycine
  • 20 mM Na2HPO4*2 H2
  • 1.5 M NaCl
  • 1 mM EDTA
  • Dissolve all substances in water.
  • Adjust pH 8 with phosphoric acid.
  • 0.2 M glycine
  • 0.05% Tween 20
  • Adjust pH 2.5 with hydrogen chloride.
  • 0.1 M TRIS-HCl, pH 9.0
  • 50 mM ethanolamine
  • 50 mM sodium phosphate, pH 8.5

Buffers

  • S30A buffer is prepared according to Sun et al. 2013 and contains
    • 14 mM Mg-glutamate
    • 60 mM K-glutamate
    • 50 mM TRIS
    at pH = 7.7 (with acetic acid), autoclaved, stored at 4 °C. Right before use, DTT is added to 2 mM final concentration.
  • S30 buffer (buffer A from Kwon and Jewett 2015) with lower TRIS concentration
    • 14 mM Mg-glutamate
    • 60 mM K-glutamate
    • 10 mM TRIS
    at pH = 8.2 (with acetic acid), autoclaved, stored at 4 °C. Right before use, DTT is added to 2 mM final concentration.

Stock solutions

  • 1.5 M Spermidine and 1 M putrescine solutions are prepared according to supporting material from Yang et al. 2012a. Briefly, a total of 4.59 mL of autoclaved MilliQ water is added in small steps to a 1 g bottle of spermidine. After each step, the bottle is mixed vigorously and the liquid is poured into a beaker where it is continously stirred. After rinsing out the whole bottle, the homogenous solution is aliquoted, flash freezed and stored at -80 °C. The procedure is similar for putrescine, though volumes differ.
  • NTP mixture is prepared from ATP, CTP, GTP and UTP stock solutions (100 mM) from Thermo Scientific. 20x NTP premix contains 30 mM of ATP and GTP, 18 mM CTP and UTP.
  • 330 mM Phosphoenolpyruvate (PEP) stock solution is prepared and pH is adjusted with 5 M KOH according to supporting material from Yang et al. 2012a

Other

  • 250 mM TRIS-HCl
  • 1.92 M Glycine
  • 1 % (w/v) SDS
  • pH 8.3
  • 2 g/L Coomassie Brilliant Blue R250
  • 0.5 g/L Coomassie Brilliant Blue G250
  • 25 % (v/v) Isopropanol
  • 10 % (v/v) Acetic acid
  • 7 ml Tris-HCl
  • 3 ml 37 % Glycerol
  • 0.5 M SDS
  • 0.93 g Dithiothreitol
  • 1.2 mg Bromophenol blue
  • 1.3 mL rotiphorese-gel 30
  • 6.1 mL pure water
  • 2.5 mL 0.5 M TRIS-HCl, pH 6.8
  • 0.1 mL 10% SDS
  • 50 µL 10 % ammonium persulfate
  • 5 µL TEMED
  • 4.7 mL rotiphorese-gel 30
  • 2.7 mL pure water
  • 2.5 mL 0.5 M TRIS-HCl, pH 6.8
  • 0.1 mL 10% SDS
  • 50 µL 10 % ammonium persulfate
  • 10 µL TEMED
  • For 1 liter destaining solution:
    • 450 mL ethanol
    • 100 mL acetic acid
    • Fill the bottle with deionized H2O

  • p-phenylen-diisothiocyanate
  • Dissolve in pure ethanol.