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Human Small Airway Epithelial Cells-CF
Cat.No.: CSC-C8083L
Species: Human
Source: Lung
Cell Type: Epithelial
- Specification
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- Customer Review
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.
Applications:
Gene ex
Phenotypic changes to compounds
Transfect diseased cells
Cystic Fibrosis
Airway remodeling studies
Cellular interactions
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HSMC are cryopreserved as secondary cells, e.g. cells are isolated from the stated tissue and expanded in culture vessels twice before cryopreservation.
HAoSMC are isolated from human aorta (ascending and/or descending).
HPASMC are isolated from human pulmonary artery.
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HBTSMC are isolated from the trachea and primary bronchi.
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HSMC are extensively tested to meet quality standards and exhibit optimal performance.
Creative Bioarray guarantees performance and quality.
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