Creative Biolabs-Immuno-oncology

Fibrosis Biomarker Panel Screening Service

Our Fibrosis Biomarker Panel Screening Service offers a specialized platform for identifying biomarkers associated with fibrosis progression and evaluating potential therapeutic agents. Chronic damage can cause fibrosis, a pathological reaction that disrupts normal tissue architecture and causes an abnormal buildup of extracellular matrix (ECM) components. It is a prevalent characteristic of many chronic diseases, including idiopathic pulmonary fibrosis (IPF), chronic kidney disease (CKD), and liver cirrhosis. It can occur in the liver, lungs, kidneys, and heart, among other organs.

Fibrosis and Biomarkers: An Overview

Fibrosis is characterized by an abnormal wound-healing response, leading to the deposition of collagen and other ECM components in tissues. This process can result from chronic inflammation, oxidative stress, or mechanical injury, and is mediated by various signaling pathways such as TGF-β (transforming growth factor beta), Wnt/β-catenin, and PDGF (platelet-derived growth factor). The progressive deposition of ECM leads to tissue scarring, organ dysfunction, and eventually organ failure.

Fibrosis Biomarker Panel Screening Service at Creative Biolabs

This service provides an in-depth analysis of key biomarkers involved in the fibrotic process, helping researchers identify novel targets, validate biomarkers for clinical use, and evaluate therapeutic candidates in preclinical drug discovery models. Through a combination of high-throughput assays, cellular models, and advanced data analysis, our service accelerates the discovery of effective treatments for fibrosis.

Our panel covers a broad range of fibrosis-related biomarkers, including but not limited to:

Extracellular matrix (ECM) markers: Collagen types (I, III), fibronectin, elastin.

Fibrosis-related enzymes: MMPs, TIMPs, and lysyl oxidase (LOX).

Inflammatory cytokines and growth factors: TGF-β1, PDGF, IL-6, and TNF-α.

Fibroblast activation markers: α-SMA, vimentin.

Cellular stress markers: HSP70 (heat shock protein), PAI-1 (plasminogen activator inhibitor-1).

We use both primary and immortalized cell lines, such as human hepatic stellate cells (HSCs), lung fibroblasts, and kidney fibroblasts, to model the fibrotic process in vitro. These assays can evaluate:

Fibroblast activation: Monitoring markers like α-SMA and collagen deposition in response to profibrotic stimuli.

ECM production: Measuring collagen secretion and ECM remodeling by fibroblasts or other fibrogenic cells.

Inflammatory response: Assessing cytokine secretion or expression of inflammatory markers during fibrosis induction.

Fig.1 Process. (Creative Biolabs Original)

We offer the ability to screen large compound libraries to identify potential antifibrotic agents. The screening can include small molecules, biologics, or natural product extracts. Compounds are evaluated for their capacity to alter fibrosis-related biomarker expression or activity.

We can explore the underlying molecular mechanisms of candidate compounds, such as their effects on key fibrotic pathways (e.g., TGF-β/Smad, Wnt/β-catenin, Notch) and their ability to regulate fibroblast-to-myofibroblast differentiation.

Depending on the specific research requirements, we can tailor the biomarker panel to focus on fibrosis in specific organs or tissues (e.g., liver, kidney, lung), or to investigate particular fibrosis subtypes (e.g., idiopathic pulmonary fibrosis, liver cirrhosis).

Unique Features of Our Services

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If you're ready to explore novel fibrosis biomarkers or evaluate antifibrotic therapies, we invite you to get in touch with us. Our team is ready to discuss your research needs, provide a tailored quote, and offer detailed information on how our services can accelerate your drug discovery process.

For Research Use Only | Not For Clinical Use

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