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Merck

Primary epithelial cell models for cystic fibrosis research.

Methods in molecular biology (Clifton, N.J.) (2011-05-07)
Scott H Randell, M Leslie Fulcher, Wanda O'Neal, John C Olsen
ZUSAMMENFASSUNG

When primary human airway epithelial (hAE) cells are grown in vitro on porous supports at an air-liquid interface (ALI), they recapitulate in vivo morphology and key physiologic processes. These cultures are useful for studying respiratory tract biology and diseases and for testing new cystic fibrosis (CF) therapies. This chapter gives protocols enabling creation of well-differentiated primary CF and non-CF airway epithelial cell cultures with non-proprietary reagents. We also discuss the production of retroviral and lentiviral vectors, the derivation of hAE cell lines, reporter gene assays, and the evolving science of gene overexpression and knockdown in ALI hAE cultures.

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Sigma-Aldrich
Deoxyribonuclease I aus Rinderpankreas, lyophilized powder, Protein ≥85 %, ≥400 Kunitz units/mg protein
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Protease aus Streptomyces griseus, Type XIV, ≥3.5 units/mg solid, powder
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holo-Transferrin human, powder, BioReagent, suitable for cell culture, ≥97%
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Collagenase aus Clostridium histolyticum, suitable for release of physiologically active rat epididymal adipocytes, Type II, 0.5-5.0 FALGPA units/mg solid, ≥125 CDU/mg solid
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3,3′,5-Triiod-L-thyronin Natriumsalz, powder, BioReagent, suitable for cell culture
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Albumin aus Rinderserum, lyophilized powder, essentially globulin free, ≥99% (agarose gel electrophoresis)
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Kollagen aus menschlicher Placenta, Bornstein and Traub Type IV, powder
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(−)-Epinephrin
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Trypsin-Inhibitor aus Glycine max (soybean), lyophilized powder
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Hydrokortison - wasserlöslich, BioReagent, suitable for cell culture
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Adenosin-5′-triphosphat Dinatriumsalz Hydrat, Grade II, ≥97% (HPLC), crystalline, from microbial
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Natriummetasilikat Nonahydrat, BioReagent, suitable for plant cell culture, ≥98%