ACKR3 ( non-phos, C-Term ), Atypical Chemokine Receptor 3 Polyclonal Antibody

ACKR3 ( non-phos, C-Term ), Atypical Chemokine Receptor 3 Polyclonal Antibody

Catalog Number:
A001455912TMA
Mfr. No.:
7TM0080N
Price:
$450
  • Size:
    100 µl
    Quantity:
    Add to Cart:
      • Overview
        • The non-phospho-ACKR3 receptor antibody is directed against the carboxyl-terminal tail of mouse, rat and human ACKR3/CXCR7. It can be used to detect total ACKR3 receptors in Western blots independent of phosphorylation. The non-phospho-ACKR3 antibody can also be used to isolate and enrich ACKR3 receptors from cell and tissue lysates.

          Please contact us at for specific academic pricing.

      • Properties
        • Host
          rabbit
          Antibody Type
          polyclonal
          Isotype
          IgG
          Reactivity
          human; mouse; rat
          Immunogen
          A synthetic peptide presents part of carboxyl-terminal tail which is identical in human, mouse and rat ACKR3
          Purification
          Antigen affinity chromatography
          Formulation
          Liquid
          Storage
          Short-term storage at 4°C and long-term storage at -20°C
          Antigen
          ACKR3, CXCR7, Atypical Chemokin Receptor 3, CXC Chemokin Receptor 7 (UniProt:P25106(human), P56485 (mouse), O89039 (rat))

          * This product is intended for research use only.

      • Applications
        • Application
          WB
        • Application Dilutions
          Western Blot (WB) 1:1000
      • Reference
        • 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.
          Sánchez-Alcañiz JA, Haege S, Mueller W, Pla R, Mackay F, Schulz S, López-Bendito G, Stumm R, Marín O. Cxcr7 controls neuronal migration by regulating chemokine responsiveness. Neuron. 2011 Jan 13;69(1):77-90. doi: 10.1016/j.neuron.2010.12.006.
          Hoffmann F, Müller W, Schütz D, Penfold ME, Wong YH, Schulz S, Stumm R. Rapid uptake and degradation of CXCL12 depend on CXCR7 carboxyl-terminal serine/threonine residues. J Biol Chem. 2012 Aug 17;287(34):28362-77. doi: 10.1074/jbc.M111.335679. Epub 2012 Jun 26. PubMed PMID: 22736769; PubMed Central PMCID: PMC3436560.

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