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Nevada Proteomics Center

Phone(775) 784-6337: 2-D Gels
Phone(775) 784-1590: Mass Spectrometry
Fax(775) 784-1419
Emailquilici@unr.edu
Location School of Medicine
Manville Medical Building, Rooms 15-17, MS 0330
Address 1664 N. Virginia Street
Reno,  NV  89557-MS 0330
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Protocol: Phenol/Ammonium Acetate-Methanol Precipitation

This method can be very useful for solubilizing proteins from plant membranes.

  • Suspend membrane pellet in 0.5 ml of extraction buffer (0.7 M sucrose, 0.5 M Tris, 30 mM HCl, 50 mM EDTA, 0.1 M KCl , 2% (v/v) 2-mercaptoethanol and 2 mM PMSF).
  • Homogenize with a glass homogenizer fitted with a Teflon plunger.
  • Adjust sample to 1.5 ml with extraction buffer. Incubate for 10 min at 4°C.
  • Add an equal volume of water-saturated phenol. Shake at room temperature for 10 min.
  • Separate the phases by centrifugation.
  • Recover the phenol phase and re-extract with an equal volume of extraction buffer.
  • Precipitate proteins from the phenol phase by addition of 5 volumes of 0.1 M ammonium acetate in methanol. Incubate at -20°C overnight.
  • Wash the precipitate 3 times with ammonium acetate in methanol and 1 time with acetone. Air dry the pellet.
  • Solubilize in rehydration buffer by incubation for 1 hour at room temperature.
  • Remove insoluble material by centrifugation (178,000 x g for 15 min).

Reference: Westermeier, Reiner (2006) Preparation of plant samples for 2-D electrophoresis, Practical Proteomics 1-2, 56-60.

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University of Nevada, Reno

University of Nevada, Reno
1664 N. Virginia Street
Reno,  NV  89557-

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