For research use only
| Cat No. | ABC-TC3929 |
| Product Type | Mouse Primary Cells |
| Cell Type | Fibroblast |
| Species | Mouse |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Intestine |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Mouse intestinal fibroblasts, 2-week C57B mouse.
Mouse Intestinal Fibroblasts are primary cells isolated from the intestinal tissue of healthy mice. They exhibit a typical spindle-shaped morphology with adherent growth. Functionally, these specialized mesenchymal cells play a key role in maintaining intestinal barrier integrity, synthesizing extracellular matrix components, and regulating inflammatory responses. Dysregulation of these cells is linked to inflammatory bowel diseases (IBD) like Crohn’s disease and ulcerative colitis. The cells express vimentin. These cells have limited proliferative capacity in vitro. 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 | Mouse Intestinal Fibroblasts, Murine Gut Fibroblasts, Intestinal Stromal Cells (Mouse), Mouse Enteric Fibroblasts |
| Species | Mouse |
| Cat.No | ABC-TC3929 |
| 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 | Intestine |
| 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. |
Mouse Intestinal Fibroblasts serve as a relevant in vitro cellular model for investigating the pathophysiological processes of inflammatory bowel diseases (IBD), such as Crohn’s disease and ulcerative colitis. For example, by investigating their secretion of extracellular matrix proteins and pro-inflammatory cytokines in response to microbial or immune stimuli, researchers can explore molecular pathways underlying intestinal fibrosis and chronic inflammation. This supports discovery research and molecular target identification related to IBD and gastrointestinal fibrosis associated with dysregulated intestinal fibroblast function in tissue repair, excessive scarring and barrier dysfunction.
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