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CXC Chemokine Receptor 6 Antibodies

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CXCR6 (non-phospho), CXCR6 Chemokine Receptor Antibody
CXCR6 (non-phospho), CXCR6 Chemokine Receptor...
The non-phospho-CXCR6 receptor antibody is directed against the distal end of the carboxyl-terminal tail of human CXCR6. It can be used to detect total CXCR6 receptors in Western blots independent of phosphorylation.
$ 375.00 *
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Agonist-induced Serine320/Serine321 phosphorylation of the CXC Chemokine Receptor 6
pS320/pS321-CXCR6 (phospho-CXC Chemokine...
Serine320/Serine321 (S320/S321) is a major phosphorylation site of the CXCR6 receptor. The pS320/pS321-CXCR6 antibody detects phosphorylation in response to high- and low-efficacy agonists but not after PKC activation. S320/S321...
$ 375.00 *
NEW
 Agonist-induced Serine325/Threonine327 phosphorylation of the CXC Chemokine Receptor 6
pS325/pT327-CXCR6 (phospho-CXC Chemokine...
Serine325/Threonine327 (S325/T327) is a major phosphorylation site of the CXCR6 receptor. The pS325/pT327-CXCR6 antibody detects phosphorylation in response to high- and low-efficacy agonists but not after PKC activation. S325/T327...
$ 375.00 *
NEW
Agonist-induced Serine329/Serine331 phosphorylation of the CXC Chemokine Receptor 6
pS329/pS331-CXCR6 (phospho-CXC Chemokine...
Serine329/Serine331 (S329/S331) is a major phosphorylation site of the CXCR6 receptor. The pS329/pS331-CXCR6 antibody detects phosphorylation in response to high- and low-efficacy agonists and after PKC activation. S329/S331...
$ 375.00 *

CXCR6

C-X-C chemokine receptor 6 (CXCR6, formerly CXCR6/Bonzo or STRL33) is a class A G protein-coupled receptor whose only known endogenous ligand is CXCL16. CXCL16 is synthesized as a transmembrane protein that can support adhesion of CXCR6-expressing cells. Proteolytic shedding, mediated principally by ADAM10, releases soluble CXCL16, which acts as a chemoattractant. CXCR6 is expressed on subsets of activated and memory T cells, including tissue-resident CD8⁺ T cells, as well as on natural killer T cells and some natural killer cells. The CXCL16–CXCR6 axis helps position and retain lymphocytes in tissues such as the liver, lung, and skin and can support antitumor T-cell responses. Inflammatory cytokines can increase CXCL16 expression, thereby regulating the availability of the ligand in inflamed tissues. Soluble CXCL16 can induce CXCR6 internalization, followed by recycling of the receptor to the cell surface. Selective small-molecule antagonists such as ML339 have been developed as preclinical research tools. No selective CXCR6 agonist or antagonist has been reported to enter clinical trials or receive approval for therapeutic use. CXCR6 desensitization, β-arrestin recruitment and internalization are regulated by phosphorylation of carboxyl-terminal serine320/serine321 (pS320/pS321-CXCR6), serine325/threonine327 (pS325/pT327-CXCR6) and serine329/serine331 (pS329/pS331-CXCR6) residues. This nomenclature refers to the human CXCR6. This phosphorylation motif is highly conserved across species and is also present in mice and rats. For more information on CXCR6 pharmacology please refer to the IUPHAR database. For further reading refer to:

Bachelerie F, Ben-Baruch A, Burkhardt AM, Combadiere C, Farber JM, Graham GJ, Horuk R, Sparre-Ulrich AH, Locati M, Luster AD, Mantovani A, Matsushima K, Murphy PM, Nibbs R, Nomiyama H, Power CA, Proudfoot AE, Rosenkilde MM, Rot A, Sozzani S, Thelen M, Yoshie O, Zlotnik A. International Union of Basic and Clinical Pharmacology. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors. Pharmacol Rev. 2013 Nov 11;66(1):1-79. doi: 10.1124/pr.113.007724. Print 2014. Review. Erratum in: Pharmacol Rev. 2014 Apr;66(2):467. PubMed PMID: 24218476; PubMed Central PMCID: PMC3880466.

C-X-C chemokine receptor 6 (CXCR6, formerly CXCR6/Bonzo or STRL33) is a class A G protein-coupled receptor whose only known endogenous ligand is CXCL16. CXCL16 is synthesized as a... read more »
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CXC Chemokine Receptor 6 Antibodies

CXCR6

C-X-C chemokine receptor 6 (CXCR6, formerly CXCR6/Bonzo or STRL33) is a class A G protein-coupled receptor whose only known endogenous ligand is CXCL16. CXCL16 is synthesized as a transmembrane protein that can support adhesion of CXCR6-expressing cells. Proteolytic shedding, mediated principally by ADAM10, releases soluble CXCL16, which acts as a chemoattractant. CXCR6 is expressed on subsets of activated and memory T cells, including tissue-resident CD8⁺ T cells, as well as on natural killer T cells and some natural killer cells. The CXCL16–CXCR6 axis helps position and retain lymphocytes in tissues such as the liver, lung, and skin and can support antitumor T-cell responses. Inflammatory cytokines can increase CXCL16 expression, thereby regulating the availability of the ligand in inflamed tissues. Soluble CXCL16 can induce CXCR6 internalization, followed by recycling of the receptor to the cell surface. Selective small-molecule antagonists such as ML339 have been developed as preclinical research tools. No selective CXCR6 agonist or antagonist has been reported to enter clinical trials or receive approval for therapeutic use. CXCR6 desensitization, β-arrestin recruitment and internalization are regulated by phosphorylation of carboxyl-terminal serine320/serine321 (pS320/pS321-CXCR6), serine325/threonine327 (pS325/pT327-CXCR6) and serine329/serine331 (pS329/pS331-CXCR6) residues. This nomenclature refers to the human CXCR6. This phosphorylation motif is highly conserved across species and is also present in mice and rats. For more information on CXCR6 pharmacology please refer to the IUPHAR database. For further reading refer to:

Bachelerie F, Ben-Baruch A, Burkhardt AM, Combadiere C, Farber JM, Graham GJ, Horuk R, Sparre-Ulrich AH, Locati M, Luster AD, Mantovani A, Matsushima K, Murphy PM, Nibbs R, Nomiyama H, Power CA, Proudfoot AE, Rosenkilde MM, Rot A, Sozzani S, Thelen M, Yoshie O, Zlotnik A. International Union of Basic and Clinical Pharmacology. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors. Pharmacol Rev. 2013 Nov 11;66(1):1-79. doi: 10.1124/pr.113.007724. Print 2014. Review. Erratum in: Pharmacol Rev. 2014 Apr;66(2):467. PubMed PMID: 24218476; PubMed Central PMCID: PMC3880466.

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