Primary Cells

Human Bladder Fibroblasts, Secondary

  • 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.

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Description

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.

Application

  • 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.

Citation

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