For research use only
| Cat No. | ABC-TC3512 |
| Product Type | Bladder Cells |
| Cell Type | Fibroblast |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Bladder |
| Disease | Normal |
| Storage | Liquid Nitrogen |
Special edition cells are isolated from the tissue types described.
Human Bladder Fibroblasts, Secondary are primary cells isolated from human bladder tissue. They are typically obtained from non-diseased bladder samples and cryopreserved at a secondary passage to retain characteristic functions. They exhibit spindle-shaped morphology and adherent growth in a monolayer. Functionally, they contribute to the synthesis and maintenance of the bladder’s extracellular matrix for structural support, and serve as a valuable in vitro model for studying fibroblast involvement in bladder cancer, while their dysregulation is linked to bladder fibrosis and other bladder-related connective tissue disorders. These fibroblasts express vimentin. They can be passaged multiple times under appropriate cell-culture conditions. 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 Fibroblasts Secondary Culture, Secondary Bladder Fibroblasts Human, Bladder Fibroblasts Passage Cells, Human Bladder Stromal Fibroblasts Secondary, HBF-Secondary |
| Species | Human |
| Cat.No | ABC-TC3512 |
| 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 | 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 Fibroblasts, Secondary can be employed as an in vitro cell model to study the pathogenesis of bladder-related disorders such as bladder fibrosis and interstitial cystitis. Their preserved extracellular matrix regulatory functions enable investigation of TGF-β-mediated fibrotic pathways, abnormal collagen deposition, and the characteristics of matrix metalloproteinase activity. Researchers can utilize this system to get a better understanding of the normal physiological functions of bladder fibroblasts and their pathological alterations.
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