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  1. -embryos are dissected from timed-pregnant mice from 11.5 d.p.c. to 13.5 d.p.c.
  2. -metanephroi and associated ureteric buds are microdissected and placed in holding medium (L15 medium supplemented with 1 x MITO+ serum extender) (all media is supplemented with 100 U penicillin/ml and 0.1 mg streptomycin/ml)
  3. -metanephroi are allowed to sit in holding medium anywhere from 20 min to 2 hours
  4. -0.2 ml of serum-free explant media (DMEM-F12 medium supplemented with 5 x MITO+ with or without 10% fetal bovine serum) is added to each well of a six-well tissue culture plate containing Cyclopore (polyethylene terphthalate; Falcon Labware) inserts
  5. -metanephroi are transferred from the holding media onto the surface of the Cyclopore membranes (for transfer, the end of a 200 Ál pipette tip is removed with a sterile razor blade (to enlarge the hole), and metanephroi are taken up in 5 – 10 Ál of holding media)
  6. -metanephroi are grown on the tissue culture inserts in a 37oC incubator under an atmosphere of 5% CO2
  7. -explant media is replaced every 48 hours

Metanephroi can be successfully grown for 7 – 10 days