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- Order number: 7TM0080A
- Content: 100 µl
- Host: Rabbit
Serine350/Threonine352 (S350/T352) is major phosphorylation site of the Atypical Chemokine Receptor 3 (ACKR3, previously called CXCR7). The pS350/pT352-ACKR3 antibody detects phosphorylation in response to agonists and after PKC activation. S350/T352 phosphorylation is required for efficient ligand sequestration by ACKR3.
Alternative Names | ACKR3, CXCR7, Atypical Chemokine Receptor 3, CXC Chemokine Receptor 7 |
IUPHAR Target ID | 80 |
UniProt ID | P25106 (human) P56485 (mouse) |
Western Blot (WB) | 1:1000 |
Species Reactivity | Human, Mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Immunogen | A synthetic phosphopeptide derived from human ACKR3 around the phosphorylation site of Ser350/Thr352 |
Form | Liquid |
Purification | Antigen affinity chromatography |
Storage buffer | Dulbecco's PBS, pH 7.4, with 150 mM NaCl, 0.02% sodium azide |
Storage conditions | short-term 4°C, long-term -20°C |
Figure 1. Agonist-induced Serine350/Threonine352 phosphorylation of the Atypical Chemokine Receptor 3/CXC Chemokine Receptor 7. Upper panel, HEK293 cells stably expressing the Atypical Chemokine Receptor 3/CXC Chemokine Receptor 7 (ACKR3/CXCR7) were either not exposed or exposed to 100 nM CXCL12 or 0.1 μM PMA (Phorbol 12-Myristate 13-Acetate) for 30 minutes. Cells were lysed and immunoblotted with the anti-pS350/pT352-ACKR3/CXCR7 antibody (7TM0080A) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-ACKR3/CXCR7 antibody (7TM0080N-WB) at a dilution of 1:1000 to confirm equal loading of the gel.
Figure 2. Analysis of dose-dependent Atypical Chemokine Receptor 3/CXC Chemokine Receptor 7 phosphorylation. Upper panel, HEK293 cells stably expressing the Atypical Chemokine Receptor 3/CXC Chemokine Receptor 7 (ACKR3/CXCR7) were either not exposed or exposed to increasing concentrations of CXCL12 ranging from 5 to 250 nM for 30 minutes. Cells were lysed and immunoblotted with the anti-pS350/pT352-ACKR3/CXCR7 antibody (7TM0080A) at a dilution of 1:1000. Lower panel, blot was stripped and reprobed with the phosphorylation-independent anti-ACKR3/CXCR7 antibody (7TM0080N-WB) at a dilution of 1:1000 to confirm equal loading of the gel.
Saaber F, Schütz D, Miess E, Abe P, Desikan S, Ashok Kumar P, Balk S, Huang K, Beaulieu JM, Schulz S, Stumm R. ACKR3 Regulation of Neuronal Migration Requires ACKR3 Phosphorylation, but Not β-Arrestin. Cell Rep. 2019 Feb 5;26(6):1473-1488.e9. doi: 10.1016/j.celrep.2019.01.049. PubMed PMID: 30726732.