Date published: 2026-4-24

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GALR Activators

Santa Cruz Biotechnology now offers a broad range of GALR Activators for use in various applications. Galanin receptors (GALRs) are a family of G-protein coupled receptors that play a pivotal role in regulating a wide array of physiological processes, including modulation of neurotransmission, hormone release, and appetite control. These receptors, which include subtypes GALR1, GALR2, and GALR3, are activated by the neuropeptide galanin, influencing several key functions within the central and peripheral nervous systems. GALR Activators are essential tools in scientific research, allowing researchers to study the specific roles of these receptors in various biological contexts. By activating GALRs, scientists can explore how these receptors contribute to the regulation of mood, pain perception, and neuroendocrine functions, as well as their involvement in more complex processes like neuroprotection and neuroplasticity. These activators are widely used in neurobiological research, behavioral studies, and pharmacological experiments to investigate the mechanisms of galanin signaling and its implications for conditions such as mood disorders, neurodegenerative diseases, and metabolic dysfunctions. Additionally, GALR Activators are valuable for exploring the potential of modulating galanin receptor activity to address various neurological and physiological disorders. The availability of these activators has significantly advanced research in fields such as neuroscience and endocrinology, offering crucial insights into the intricate dynamics of galanin signaling pathways. View detailed information on our available GALR Activators by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Galanin (1-30) (human)

119418-04-1sc-391141
sc-391141A
sc-391141B
sc-391141C
500 µg
1 mg
2.5 mg
5 mg
$219.00
$346.00
$575.00
$832.00
(0)

Galanin (1-30) is a neuropeptide that selectively activates galanin receptors, influencing various signaling pathways. Its unique sequence allows for specific binding interactions, modulating intracellular calcium levels and cyclic AMP production. The peptide's conformational flexibility enhances its ability to engage with receptor sites, leading to distinct physiological responses. Additionally, its stability in physiological conditions supports prolonged signaling, making it a key player in neuroendocrine regulation.