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Introduction
Primary Human Intestinal Epithelial Cells (ACBRI 519) were initiated by elutriation of dispase dissociated normal human small intestine tissue.
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Cell Initiation
These cells were originated using CSC Complete Serum-Free Medium (SF-4Z0-500), are available at < 12 Cumulative Population Doublings (CPD) in vitro [Passage 3] and were cryopreserved in aliquots of ~ 1.5 X 106 cells. This vial will initiate a Passage 4 cell culture in a 75cm2 flask.
These cells are available in cryopreserved vials as well as in 25cm2 and 75cm2 proliferating cell culture flasks.
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Monolayer Culture Phase-Contrast Digital Image (40X) Passage 5
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Companion Products
Each vial or flask of cells is shipped to Customer with Bac-Off® (antibiotic) and CultureBoost (animal derived growth factors) or CultureBoost-R (human recombinant growth factors) at no additional cost.
These cells are qualified for use with: CSC Complete Serum Free Medium (SF-4Z0-500) and CSC Complete Medium which includes 10% serum (4Z0-500); CSC Attachment Factor™ (4Z0-210); CSC Passage Reagent Group™ (4Z0-800) and CSC Cell Freezing Medium (4Z0-705).
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Cell Growth Images
Cell growth images are available.
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Standard Tests
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TEST
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RESULTS
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HIV Serologic Test (donor level HIV AB EIA)
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Negative
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HIV PCR TEST (frozen cell pool by CLIA Licensed Clinical Lab)
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Negative
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Test of frozen cells for Mycoplasma spp. (ATCC method by CLIA Licensed Clinical Lab)
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Negative
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Miscellaneous Tests
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TEST
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RESULTS
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Cytoplasmic Vimentin Intermediate Filaments
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> 02% positive by indirect immunofluorescence
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Cytoplasmic Cytokeratin Intermediate Filament
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> 95% positive by indirect immunofluorescence
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Additional Information
Functional Test: Barrier Formation
Primary Human Intestinal Epithelial Cells can provide a useful tool for absorption and permeability studies of the small intestine. ACBRI 519 cells demonstrate markers of epithelial differentiation (microvilli, desmosomes, cellular interdigitation) similar to those observed in vivo. The morphological and immunofluorescent markers demonstrated by ACBRI 519 are suggestive of a differentiated monolayer barrier that may be used to predict the absorption and transport of drugs and compounds across the mucosal barrier of the human small intestine. Plated in CSC Serum-Free Maintenance Medium (SF-4ZM-500), ACBRI 519 monolayers were tested for active barrier formation as measured by 90-minute C-Albumin flux (apical to basolateral) across the filter insert. Generation of peroxide by addition of 0.1 U/mL glucose oxidase to apical aspect of cells 30 minutes prior to albumin loading served as the positive control.
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| PMID |
Title |
Author |
Year |
| 21109446 |
Enzymatic synthesis of 125/131I labled 8-hydroxyquinoline glucuronide and in vitro/in vivo evaluation of biological infulence |
Reyhan Yesilagac |
2011 |
| 20578839 |
Enzymatic Synthesis of Uracil Glucuronide, Labeling with 125/131I, and In Vitro Evaluation on Adenocarcinoma Cells |
Ilker Emin Medine |
2010 |
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