For research use only
| Cat No. | ABC-TC3515 |
| Product Type | Bladder Cells |
| Cell Type | Stromal Fibroblast |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Bladder |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Fibroblasts are mesenchymal cells derived from the embryonic mesoderm.
Human Bladder Stromal Fibroblasts are primary cells isolated from the healthy human urinary bladder tissue, cryopreserved to retain their native biological properties. They exhibit spindle-shaped morphology and adherent growth in a monolayer. Functionally, they contribute to normal bladder tissue homeostasis synthesizing and organizing the bladder stroma’s extracellular matrix (ECM). Their abnormalities have been shown to be associated with bladder diseases like interstitial cystitis and fibrosis. These fibroblasts express vimentin. They can be passaged multiple times under proper culture conditions. For optimal performance, repeated freezing and thawing should be avoided during culture. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | Human Bladder Stromal Fibroblasts, Bladder Stromal Cells Human, Human Bladder Connective Tissue Fibroblasts, HBSFs, Bladder Fibroblasts Stromal |
| Species | Human |
| Cat.No | ABC-TC3515 |
| Product Category | Primary Cells |
| Size/Quantity | 1 vial |
| Cell Type | Stromal Fibroblast |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Bladder |
| Disease | Normal |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Bladder Cells |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
Human Bladder Stromal Fibroblasts can be used as an in vitro cell model to study the pathogenesis of bladder-associated disorders such as interstitial cystitis and bladder fibrosis. Their preserved extracellular matrix regulatory functions enable investigation of critical pathological mechanisms including abnormal extracellular matrix remodeling (activation of matrix-metalloproteinases and their inhibitors), excessive collagen deposition, and TGF-β-mediated fibrotic signaling pathways. This model provides a better understanding of the normal physiological functions of these fibroblasts and the pathological changes occurring in disease states.
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