Date published: 2025-9-21

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cystatin 13 Activators

Cst13, identified as cystatin 13, emerges as a crucial player in cellular processes, leveraging its predicted function as an inhibitor of cysteine-type endopeptidases. Positioned upstream of negative regulation of peptidase activity, this gene exhibits a versatile functional role predicted to extend into both the cytoplasm and the extracellular region. The selective expression of Cst13 in the testis further emphasizes its specialization within reproductive tissues. Its orthologous relationship with human CST13P, a pseudogene, adds an intriguing layer to its evolutionary conservation, suggesting potential functional significance in maintaining cellular homeostasis and responding to environmental cues.

The activation of Cst13 involves intricate molecular mechanisms orchestrated by a diverse array of chemical activators. Direct activation pathways include histone deacetylase inhibition and DNA demethylation, fostering an open chromatin structure and demethylated gene promoter, respectively. These processes enhance Cst13 expression by creating a conducive environment for transcription. Additionally, indirect activation is achieved through inhibitors targeting critical signaling pathways such as TGF-β, MAPK/ERK, PI3K/AKT, NF-κB, STAT3, JAK/STAT, and Wnt. By blocking these pathways, negative regulation on Cst13 is alleviated, leading to increased gene expression and subsequent upregulation. This complex regulatory network underscores the adaptability of Cst13 in responding to a myriad of cellular signals, highlighting its pivotal role in maintaining cellular integrity and modulating essential cellular processes. Exploring the comprehensive landscape of Cst13 and its activation mechanisms not only advances our understanding of its function but also lays the groundwork for potential implications in broader biological contexts.

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