Selected article for: "ma cambridge and madison promega"
Title: Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers
  • Document date: 1994_7_1
    • ID: ra20actc_8
    Snippet: Enzymes used in molecular cloning were obtained from Boehringer Mannheim (Indianapolis, IN), New England Biolabs (Beverly, MA), or Promega (Madison, WI). DME (4.5 g/1 glucose) and RPMI-1640 medium were from GIBCO BRL (Grand Island, NY); FCS from Hazleton Biologics (Lenexa, KS); Nusera from Collaborative Biomedical Products (Bedford, MA); DEAE-dextran, chloroqulne, CNBr-activated Sepharose 4B, and protease inhibitors were from Sigma Chemical Co. (.....
    Document: Enzymes used in molecular cloning were obtained from Boehringer Mannheim (Indianapolis, IN), New England Biolabs (Beverly, MA), or Promega (Madison, WI). DME (4.5 g/1 glucose) and RPMI-1640 medium were from GIBCO BRL (Grand Island, NY); FCS from Hazleton Biologics (Lenexa, KS); Nusera from Collaborative Biomedical Products (Bedford, MA); DEAE-dextran, chloroqulne, CNBr-activated Sepharose 4B, and protease inhibitors were from Sigma Chemical Co. (St. Louis, MO); ECL western blotting reagents from Amersham Corp. (Arlington Heights, IL); nitrocellulose from Schleicher and Schuell (Keene, NH); protein A-Sepharose beads from Repligen Corporation (Cambridge, MA); FITC goat antimouse IgG from Cappel OVestchester, PA); cell culture dishes from Falcon (Becton Dickinson Co., Lincoln Park, NJ); multichamber slides from Nunc Inc. (Naperville, IL); and human plasma fibronectin from the New York Blood Center.

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