Gain unprecedented insights into Idiopathic Pulmonary Fibrosis pathogenesis and progression by specifically targeting damaged collagen with Collagen Hybridizing Peptides (CHPs)
CHP staining intensity serves as a marker for the degree of collagen remodeling, which is a hallmark of fibrotic disease activity and progression
Researchers in Idiopathic Pulmonary Fibrosis face significant hurdles in accurately replicating the progressive nature of the human disease within preclinical models. Additionally, precisely quantifying the complex dynamics of collagen, particularly its turnover and crosslinking, remains a substantial challenge in advancing our understanding and treatment of this devastating condition.
Go beyond static measurements. Explore the power of CHPs to track collagen turnover and remodeling in real-time, providing a dynamic view of IPF progression. Download our application note to see how.
CHPs enable the precise measurement of inflammation and tissue damage in a number of conditions.
Our CHP products are conjugated with a variety of detection motifs for brightfield and fluorescence detection, and they can be customized to meet your unique needs. Visit our products page to learn more.
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