For research use only
| Cat No. | ABC-TC3050 |
| Product Type | Mouse Primary Cells |
| Cell Type | Fibroblast |
| Species | B6129SF2/J Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Lung |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Mouse lung fibroblasts are isolated from tissue of pathogen-free laboratory mice.
B6129SF2/J Mouse Lung Fibroblasts are primary cells isolated from the lung tissue of B6129SF2/J mice, a hybrid strain widely used in respiratory disease research and fibroblast tissue research in B6129SF2/J mice. These fibroblasts play a vital role in maintaining extracellular matrix homeostasis and participate in wound healing, inflammation, and tissue remodeling. In vitro, they display a spindle-shaped morphology and adherent growth properties. Studies have demonstrated that lung fibroblasts contribute to the progression of pulmonary fibrosis by producing excessive collagen and fibronectin in response to profibrotic signals like TGF-β1. Expression of mesenchymal markers such as vimentin and α-smooth muscle actin is confirmed by immunocytochemistry under profibrotic conditions. They are cryopreserved at early passages to retain phenotypic fidelity Each lot undergoes rigorous screening and isolation procedures, and is rigorously tested to ensure it is free of contamination from Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | B6129SF2/J Mouse Lung Fibroblasts, B6129SF2J lung fibroblasts, Mouse lung fibroblasts B6129SF2/J |
| Species | B6129SF2/J Mouse |
| Cat.No | ABC-TC3050 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Fibroblast |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Lung |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Mouse Primary Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
B6129SF2/J Mouse Lung Fibroblasts provide a reliable in vitro model to investigate lung fibrosis, ECM regulation, and fibroblast-to-myofibroblast transition. These cells exhibit robust ECM production and myofibroblast differentiation in response to profibrotic stimuli, enabling detailed analysis of fibrosis progression and therapeutic screening. They are also valuable for studying the cellular mechanisms of idiopathic pulmonary fibrosis (IPF) and testing the efficacy of antifibrotic agents targeting TGF-β signaling or ECM turnover.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).