Premium Phosphosite-Specific 7TM Antibodies
Novel Tools for Your GPCR Research
Select Your Country of Delivery below

GPR17 Receptor Antibodies

Close filters
No results were found for the filter!
NEW
pS351/pT356-GPR17 (phospho-GPR17 Antibody)
pS351/pT356-GPR17 (phospho-GPR17 Antibody)
Serine351/Threonine356 (S351/T356) is a major phosphorylation site of the human GPR17 receptor. The pS351/pT356-GPR17 antibody detects phosphorylation in response to high-efficacy agonists. S351/T356 phosphorylation is a key regulator of...
$ 350.00 *
NEW
Validation of the G Protein-coupled Receptor 17 in transfected HEK293 cells
GPR17 (non-phospho), G Protein-coupled Receptor...
The non-phospho-GPR17 receptor antibody is directed against the distal part of the carboxyl-terminal tail of human GPR17. It can be used to detect total GPR17 receptors in Western blots independent of phosphorylation. The...
$ 350.00 *

GPR17 is an orphan GPCR. The endogenous ligand for GPR17 remains to be discovered. GPR17 has previously been reported to be a dual specificity receptor for uracil nucleotides and cysteinyl leukotrienes (CysLTs). GPR17 may mediate brain damage by nucleotides and CysLTs following ischemia. In the central nervous system, GPR17 is expressed in a subset of (pre)-oligodendrocytes and in neurogenic areas. After spinal cord injury, or focal cerebral ischaemia, GPR17 expression is induced in a population of proliferating microglial cells in the lesioned area. GPR17 is regulated by phosphorylation of carboxyl-terminal serine351/threonine356 (pS351/pT356-GPR17). This nomenclature refers to the human GPR17 receptor and is identical in mice and rats in which it corresponds to pS323/pT328-GPR17. For more information on GPR17 pharmacology please refer to the IUPHAR database. For further reading refer to:

Davenport AP, Alexander SP, Sharman JL, Pawson AJ, Benson HE, Monaghan AE, Liew WC, Mpamhanga CP, Bonner TI, Neubig RR, Pin JP, Spedding M, Harmar AJ. International Union of Basic and Clinical Pharmacology. LXXXVIII. G protein-coupled receptor list: recommendations for new pairings with cognate ligands. Pharmacol Rev. 2013 May 17;65(3):967-86. doi: 10.1124/pr.112.007179. PMID: 23686350; PMCID: PMC3698937.

Alexander SP, Battey J, Benson HE, Benya RV, Bonner TI, Davenport AP, Dhanachandra Singh K, Eguchi S, Harmar A, Holliday N, Jensen RT, Karnik S, Kostenis E, Liew WC, Monaghan AE, Mpamhanga C, Neubig R, Pawson AJ, Pin JP, Sharman JL, Spedding M, Spindel E, Stoddart L, Storjohann L, Thomas WG, Tirupula K, Vanderheyden P. Class A Orphans in GtoPdb v.2023.1. IUPHAR/BPS Guide to Pharmacology CITE. 2023; 2023(1). Available from: https://doi.org/10.2218/gtopdb/F16/2023.1.

GPR17 is an orphan GPCR. The endogenous ligand for GPR17 remains to be discovered. GPR17 has previously been reported to be a dual specificity receptor for uracil nucleotides and cysteinyl... read more »
Close window
GPR17 Receptor Antibodies

GPR17 is an orphan GPCR. The endogenous ligand for GPR17 remains to be discovered. GPR17 has previously been reported to be a dual specificity receptor for uracil nucleotides and cysteinyl leukotrienes (CysLTs). GPR17 may mediate brain damage by nucleotides and CysLTs following ischemia. In the central nervous system, GPR17 is expressed in a subset of (pre)-oligodendrocytes and in neurogenic areas. After spinal cord injury, or focal cerebral ischaemia, GPR17 expression is induced in a population of proliferating microglial cells in the lesioned area. GPR17 is regulated by phosphorylation of carboxyl-terminal serine351/threonine356 (pS351/pT356-GPR17). This nomenclature refers to the human GPR17 receptor and is identical in mice and rats in which it corresponds to pS323/pT328-GPR17. For more information on GPR17 pharmacology please refer to the IUPHAR database. For further reading refer to:

Davenport AP, Alexander SP, Sharman JL, Pawson AJ, Benson HE, Monaghan AE, Liew WC, Mpamhanga CP, Bonner TI, Neubig RR, Pin JP, Spedding M, Harmar AJ. International Union of Basic and Clinical Pharmacology. LXXXVIII. G protein-coupled receptor list: recommendations for new pairings with cognate ligands. Pharmacol Rev. 2013 May 17;65(3):967-86. doi: 10.1124/pr.112.007179. PMID: 23686350; PMCID: PMC3698937.

Alexander SP, Battey J, Benson HE, Benya RV, Bonner TI, Davenport AP, Dhanachandra Singh K, Eguchi S, Harmar A, Holliday N, Jensen RT, Karnik S, Kostenis E, Liew WC, Monaghan AE, Mpamhanga C, Neubig R, Pawson AJ, Pin JP, Sharman JL, Spedding M, Spindel E, Stoddart L, Storjohann L, Thomas WG, Tirupula K, Vanderheyden P. Class A Orphans in GtoPdb v.2023.1. IUPHAR/BPS Guide to Pharmacology CITE. 2023; 2023(1). Available from: https://doi.org/10.2218/gtopdb/F16/2023.1.

Recently viewed