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. Cryopreserved Diseased Bronchial Epithelial cells from Cystic Fibrosis Donors test negative for mycoplasma, bacteria, yeast, and fungi. HIV-1, hepatitis B and hepatitis C are not detected for all donors and/or cell lots. Certain lots are screened for specific genetic mutations. Contact our Scientific Support Team for additional information. A Certificate of Analysis is provided for each cell lot purchased.Benefits Test negative for mycoplasma, bacteria, yeast, and fungi HIV-1, Hepatitis B and Hepatitis C are not detected for all donors and/or cell lots A Certificate ofAnalysis is provided for each cell lot purchased Content & Storage Content 1 x Cryopreserved ampule of D-HBE-CF containing ≥500,000 cells
Endotoxin and Pyrogen Testing Products
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