Date published: 2025-9-5

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delta ENaC Activators

Santa Cruz Biotechnology now offers a broad range of delta ENaC Activators for use in various applications. Delta epithelial sodium channels (delta ENaC) are a subtype of the ENaC family, which are critical in regulating sodium balance, fluid homeostasis, and epithelial cell function. Delta ENaC Activators are important tools in scientific research, enabling the study of the specific mechanisms by which these channels control sodium transport across epithelial tissues, such as those in the kidneys, lungs, and colon. By activating delta ENaC, researchers can explore how these channels contribute to the regulation of electrolyte balance, blood pressure, and fluid volume within the body. These activators are widely used in electrophysiological studies, where they help explain the role of delta ENaC in cellular signaling pathways, ion channel regulation, and the broader implications of their activity in physiological processes. Additionally, delta ENaC Activators are valuable in investigations aimed at understanding how these channels are modulated by various factors, including hormones, mechanical forces, and extracellular signals. The availability of these activators has significantly advanced research in fields such as physiology, cell biology, and biochemistry, providing essential tools for dissecting the complex regulatory networks that govern ion transport and epithelial function. By offering precise control over delta ENaC activity, these activators facilitate a deeper understanding of the channel's role in maintaining homeostasis and its potential impact on health and disease. View detailed information on our available delta ENaC Activators by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Capsazepine

138977-28-3sc-201098
sc-201098A
5 mg
25 mg
$145.00
$450.00
11
(1)

Capsazepine is a selective antagonist of the delta epithelial sodium channel (ENaC), known for its unique ability to disrupt ion transport mechanisms. Its structure allows for specific binding interactions that inhibit channel activity, influencing sodium ion permeability across cellular membranes. The compound exhibits distinct kinetic properties, with a rapid onset of action that alters the electrochemical gradients. This modulation of ion flow can significantly impact cellular excitability and signaling pathways.