Date published: 2026-5-28

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Na+ CP type IV alpha Inhibitors

Santa Cruz Biotechnology now offers a broad range of Na+ CP type IV alpha Inhibitors for use in various applications. Sodium channels are integral membrane proteins that play a vital role in the generation and propagation of electrical signals in neurons, muscle cells, and other excitable tissues. The Na+ CP type IV alpha subunit is a specific isoform of voltage-gated sodium channels, which are critical in initiating action potentials and controlling the excitability of cells. Inhibitors targeting this sodium channel subtype are crucial tools in scientific research, particularly for studying the physiological and pathological roles of sodium channel activity. These inhibitors allow researchers to selectively block the Na+ CP type IV alpha channels, providing insights into their function in cellular signaling, their contribution to electrical excitability, and their involvement in various biological processes such as muscle contraction and neurotransmitter release. These inhibitors are widely used in research focused on understanding the molecular mechanisms underlying neurological disorders, cardiac arrhythmias, and other conditions where sodium channel function is disrupted. Additionally, Na+ CP type IV alpha Inhibitors are valuable in the development of new therapeutic strategies aimed at modulating sodium channel activity to treat conditions associated with aberrant electrical signaling. The availability of these inhibitors has significantly advanced research in neurobiology and cardiology, offering essential tools for exploring the complex dynamics of sodium channel regulation and its broader implications in health and disease. View detailed information on our available Na+ CP type IV alpha Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Tetracaine hydrochloride

136-47-0sc-251166
sc-251166A
5 g
25 g
$52.00
$95.00
(0)

Tetracaine hydrochloride functions as a potent sodium channel blocker, exhibiting a unique affinity for the inactivated state of the channel. Its molecular structure allows for effective binding within the channel's pore, stabilizing the inactivation gate and preventing ion flow. This interaction alters the kinetics of channel recovery, leading to prolonged effects on neuronal excitability. Additionally, the compound's hydrophilic nature enhances solubility, facilitating its diffusion across membranes.