Primary Cells

B6129SF2/J Mouse Lung Fibroblasts

  • 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.

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Description

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.

Application

  • 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.

Citation

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