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Diseased Human Lung Fibroblasts, Idiopathic Pulmonary Fibrosis

Product Name

Diseased Human Lung Fibroblasts, Idiopathic Pulmonary Fibrosis

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Product Code

DHLF-IPF

Cat.No

ABC-TC5520

Species

Human

Size/Quantity

1 vial

Shipping Info

Dry Ice

Storage

Liquid Nitrogen

Description

Lung fibroblasts are considered as the key effector cells in Idiopathic Pulmonary Fibrosis (IPF), an interstitial lung disease that commonly seen in elderly with unclear etiology. Characterized by excessive fibroproliferation and extracellular matrix accumulation, IPF is associated with progressive decline in lung function, poor diagnosis, and limited treatment option. Studies have suggested that transforming growth factor (TGF)-β induced alveolar epithelial cells (AEC) can undergo epithelial-mesenchymal transition (EMT) and serve as a source of fibroblast or myofibroblast in fibrosis. Aging is also a main contributor to IPF where senescence fibroblasts show abnormal metabolism and senescence-associated secretory phenotypes.
Why Choose Diseased Human Lung Fibroblasts, Idiopathic Pulmonary Fibrosis from AcceGen?
AcceGen Human lung fibroblasts IPF are derived from patients with idiopathic pulmonary fibrosis. IPF lung fibroblasts are isolated by enzymatic digestion and cryopreserved at passage 2. Each vial contains > 5×10^5 cells in 1 ml volume. Human primary IPF lung fibroblasts are characterized with spindle-shaped morphology and tested negative for von Willebrand factor VIII, cytokeratin 14, 18 and 19, and α-smooth muscle actin. All cells 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.

Citation Guide

When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).

Application

For research use only
Human primary IPF lung fibroblasts provide an excellent in vitro model for studying pathogenesis, etiology and regulation of IPF and other lung diseases that best resemble in vivo conditions. Lung fibroblasts from patients with idiopathic pulmonary fibrosis, differ from lung cells in several aspects, such as proliferation, apoptosis, DNA methylation and miRNA expression.

Key Features

-Backed by AcceGen advanced technology
-Cryopreserved for highest viability and plating efficiency
-Quality-tested for accurate results

Product Type

Pulmonary Cells

Product Image AcceGen Frozen Cells & Cell Lines 1 vial
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