Primary Cells

Human Bladder Stromal Fibroblasts

  • 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.

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Description

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.

Application

  • 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.

Citation

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High Viability
To succeed in cell culture
Precision and Reliability
To support a consistent result
Customization Options
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