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Substance P/NK1 Receptor Phosphorylation Assays

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OD signals in pS338/pT339-NK1 Phosphorylation Assay
pS338/pT339-NK1 Phosphorylation Assay Kit
The pS338/pT339-NK1 Phosphorylation Assay Kit allows determination of NK1 Phosphorylation in 96-well plates without the need for Western blot analysis.
CHF650.00 *
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OD signals in pT356/pT357-NK1 Phosphorylation Assay
pT356/pT357-NK1 Phosphorylation Assay Kit
The pT356/pT357-NK1 Phosphorylation Assay Kit allows determination of NK1 Phosphorylation in 96-well plates without the need for Western blot analysis.
CHF650.00 *
NEW
OD signals in pT344/pS347-NK1 Phosphorylation Assay
pT344/pS347-NK1 Phosphorylation Assay Kit
The pT344/pS347-NK1 Phosphorylation Assay Kit allows determination of NK1 Phosphorylation in 96-well plates without the need for Western blot analysis.
CHF650.00 *

NK1

Tachykinin 1 (NK1) receptor is a member of the tachykinin receptor family, which is characterized by the ability to bind tachykinin neuropeptides resulting in spasmodic contractions. Substance P (SP) is the most selective agonist towards NK1. The NK1 receptor is a 7TM receptor that associates with the G-protein q11. NK1 is widely distributed in both the central nervous system and peripheral tissues including the substantia nigra, the hypothalamus, the lateral habenula, the inferior colliculus the central amygdala, the frontal cortex and the sensorimotor cortex as well as the gastrointestinal tract. Antagonists such as aprepitant and fosaprepitant were approved for the prevention of nausea and vomiting associated with cancer chemotherapy. NK1 receptor desensitization, β-arrestin recruitment and internalization are regulated by phosphorylation of carboxyl-terminal threonine344/serine347 (pT344/pS347-NK1).This nomenclature refers to the human NK1 receptor. This phosphorylation motif is highly conserved across species but corresponds to pT344/pS346/pS347-NK1 in mice and rats. For more information on NK1 pharmacology please refer to the IUPHAR database. For further reading refer to:

Barrett J, Canning B, Coulson J, Dombrowsky E, Douglas SD, Fong TM, Heyward CY, Leeman SE, Remeshwar P. Tachykinin receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database. IUPHAR/BPS Guide to Pharmacology CITE. 2019; 2019(4).

Tachykinin 1 (NK1) receptor is a member of the tachykinin receptor family, which is characterized by the ability to bind tachykinin neuropeptides resulting in spasmodic contractions. Substance... read more »
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Substance P/NK1 Receptor Phosphorylation Assays

NK1

Tachykinin 1 (NK1) receptor is a member of the tachykinin receptor family, which is characterized by the ability to bind tachykinin neuropeptides resulting in spasmodic contractions. Substance P (SP) is the most selective agonist towards NK1. The NK1 receptor is a 7TM receptor that associates with the G-protein q11. NK1 is widely distributed in both the central nervous system and peripheral tissues including the substantia nigra, the hypothalamus, the lateral habenula, the inferior colliculus the central amygdala, the frontal cortex and the sensorimotor cortex as well as the gastrointestinal tract. Antagonists such as aprepitant and fosaprepitant were approved for the prevention of nausea and vomiting associated with cancer chemotherapy. NK1 receptor desensitization, β-arrestin recruitment and internalization are regulated by phosphorylation of carboxyl-terminal threonine344/serine347 (pT344/pS347-NK1).This nomenclature refers to the human NK1 receptor. This phosphorylation motif is highly conserved across species but corresponds to pT344/pS346/pS347-NK1 in mice and rats. For more information on NK1 pharmacology please refer to the IUPHAR database. For further reading refer to:

Barrett J, Canning B, Coulson J, Dombrowsky E, Douglas SD, Fong TM, Heyward CY, Leeman SE, Remeshwar P. Tachykinin receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database. IUPHAR/BPS Guide to Pharmacology CITE. 2019; 2019(4).

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