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D-HBE-CF – Diseased Human Bronchial/Tracheal Epithelial Cells – Cystic Fibrosis

D-HBE-CF – Diseased Human Bronchial/Tracheal Epithelial Cells – Cystic Fibrosis

Catalog #: 00196979
D-HBE-CF – Diseased Human Bronchial/Tracheal Epithelial Cells from donors having Cystis Fibrosis
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 3’087.00 CHF
AMP

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.

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.

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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

 

Storage and Content

1 x Cryopreserved ampule of D-HBE-CF containing ≥500,000 cells

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SDS, CoA, and Instructions

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.

  • Instructions - Airway Epithelial Cell Systems

    Instructions for Proper Use and Culture of Airway Epithelial Cells
  • TechSheet - Bronchial, Tracheal Epithelial Cell Systems

    Technical information sheet for Clonetics™ Bronchial and Tracheal cells
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