Idiopathic pulmonary fibrosis is a chronic, progressIVe lung disease that results in scarring (fibrosis) of the lungs. Clinical data may include: Medication (current and historical), Disease severity, Lung function test results (FEV1, FEVC, PEF).
Categories
Primary Cells
Species
Human
Applications
For research use only
Shipping
Dry Ice
Storage
Liquid Nitrogen
Quality Control
All cells test negatIVe for mycoplasma, bacteria, yeast, and fungi.
Reviews of Human Idiopathic Pulmonary Fibrosis (IPF) Peripheral Blood Mononuclear Cells