Product Overview
Cystic fibrosis is a disease that causes thick, sticky mucus to build up in the lungs, digestive tract, and other areas of the body. It is one of the most common chronic lung diseases in children and young adults. The disease is the most common, deadly, inherited disorder affecting Caucasians in the United States. The disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is approximately 37 years, a dramatic increase over the last three decades.
Lonza's Human Small Airway Epithelial Cells (SAEC) are isolated from cystic fibrosis human lung tissue. Cryopreserved CloneticsTM SAECs are guaranteed through 15 population doublings and stain positive for cytokeratin 19. All cells testnegative for mycoplasma, bacteria, yeast, and fungi. HIV-1, hepatitis B andhepatitis C are not detected for all donors and/or cell lots. A Certificate of Analysis is provided for each cell lot purchased.
Request More InfoStorage and Content
1 x Cryopreserved Ampule with ≥500,000 cells/vial
SDS, CoA, and Instructions
Safety Data Sheets (SDS)
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Certificate of Analysis (CoA)
Please enter Lot Number, including all zeros, located on the product label and please take into account that it is case sensitive.
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Instructions - Airway Epithelial Cell Systems
Instructions for Proper Use and Culture of Airway Epithelial Cells -
Primary Cells and Media Reference Guide
A comprehensive collection of Lonza primary cell and media products supporting many research areas.
Educational Material
Brochures, White Papers etc.
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Primary Human Airway Cells and Media
Airway Cell and Media Reference Guide -
Primary Cells and Media Reference Guide
A comprehensive collection of Lonza primary cell and media products supporting many research areas. -
Primary Cells for Airway Research – Infographic
Infographic showing how Lonza primary cells can aide in your airway research
