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Lonza Walkersville DHLF-IPF - Diseased Human Lung Fibroblasts, Idiopathic Pulmonary Fibrosis

Catalog No. NC1410251
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IPF (Idiopathic Pulmonary Fibrosis) is a fatal disease that usually affects adults between the ages of 50-70. The disease is characterized by progressive decline in lung function resulting from scarring of lung tissue.Benefits:Gene expression pathways Phenotypic changes to compounds Transfect diseased cells Co-culture with immune cells Airway remodeling studies Cellular interactionContent:1 x Cryopreserved ampule of DHLF-IPF containing ≥500,000 cells

Catalog No. NC1410251 Supplier Lonza Walkersville Supplier No. CC7231
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IPF (Idiopathic Pulmonary Fibrosis) is a fatal disease that usually affects adults between the ages of 50-70. The disease is characterized by progressive decline in lung function resulting from scarring of lung tissue.Benefits:Gene expression pathways Phenotypic changes to compounds Transfect diseased cells Co-culture with immune cells Airway remodeling studies Cellular interactionContent:1 x Cryopreserved ampule of DHLF-IPF containing ≥500,000 cells

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