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Cell Culture Core

eagle-i ID


Resource Type

  1. Core Laboratory


  1. Resource Description
    The Cell Culture Core maintains a centralized repository of cells and reagents pertinent to digestive, liver and pancreatic disease research. It also provides training (especially for students and postdoc fellows) for labs in new cell culture (2D and 3D) techniques. Cells lines are established from freshly obtained surgical specimens, all aspects of which are approved by the University of Pennsylvania Institutional Review Board. Adenoviral, retroviral and lentiviral constructs are created, propagated and maintained under institutional guidelines for biohazardous materials. Provided is a listing of items currently carried by the Cell Culture Core: 1) Lists of available GI cancers and engineered human and mouse esophageal epithelial cells. 2) Protocol for human esophageal epithelial cell culture. 3) Protocol for mouse esophageal epithelial cell culture. 4) Protocol for soybean trypsin inhibitor preparation used for mouse and human esophageal cell culture. 5) Protocol for organotypic 3D culture. 6) Basic Sterile Techniques. Normal human cell lines 1) colonic enterocytes 2) esophageal keratinocytes 3) fibrobasts and smooth muscle cells 4) endothelial cells 5) Organotypic (three dimensional) culture systems: colonocytes or esophageal keratinocytes with a substrate of fibroblasts, smooth muscle cells and endothelial cells. Malignant Cell Lines Well-characterized human cell lines originating from carcinomas of the following: 1) colon and rectum 2) esophagus 3) pancreas 4) stomach 5) liver Also, techniques are available to isolate fibroblasts.
  2. Affiliation
    Center for Molecular Studies in Digestive and Liver Diseases
  3. Website(s)
  4. Director
    Robertson, Erle., PhD
Provenance Metadata About This Resource Record
  1. workflow state
  2. contributor
    ggrant (Gregory Grant)
  3. created
  4. creator
    ggrant (Gregory Grant)
  5. modified
Copyright © 2016 by the President and Fellows of Harvard College
The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016