Human IL-3R alpha/CD123 PerCP-conjugated Antibody

Catalog # Availability Size / Price Qty
FAB301C
Detection of IL‑3 R alpha /CD123 in Human Blood Lymphocytes by Flow Cytometry.
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Product Details
Citations (8)
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Human IL-3R alpha/CD123 PerCP-conjugated Antibody Summary

Species Reactivity
Human
Specificity
Detects human IL‑3 R alpha /CD123 in direct ELISAs and Western blots.
Source
Monoclonal Mouse IgG1 Clone # 32703
Purification
Protein A or G purified from hybridoma culture supernatant
Immunogen
S. frugiperda insect ovarian cell line Sf 21-derived recombinant human IL‑3 R alpha /CD123
Lys20-Arg305, predicted
Accession # P26951
Formulation
Supplied in a saline solution containing BSA and Sodium Azide.
Label
PerCP (Peridinin-chlorophyll Protein Complex) (Excitation= 482 and 564 nm, Emission= 675 nm)

Applications

Recommended Concentration
Sample
Flow Cytometry
10 µL/106 cells
THP-1 cells

Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.

Scientific Data

Flow Cytometry Detection of IL‑3 Ra/CD123 antibody in Human Blood Lymphocytes antibody by Flow Cytometry. View Larger

Detection of IL‑3 R alpha /CD123 in Human Blood Lymphocytes by Flow Cytometry. Human peripheral blood lymphocytes were stained with Mouse Anti-Human HLA-DR PE-conjugated Monoclonal Antibody (FAB4869P) and either (A) Mouse Anti-Human IL-3 Ra/CD123 PerCP-conjugated Monoclonal Antibody (Catalog # FAB301C) or (B) Mouse IgG1PerCP Isotype Control (IC002C). View our protocol for Staining Membrane-associated Proteins.

Flow Cytometry View Larger

Detection of IL-3R alpha/CD123 in THP-1 cells by Flow Cytometry THP-1 cells were stained with Mouse Anti-Human IL-3R alpha/CD123 PerCP‑conjugated Monoclonal Antibody (Catalog # FAB301C, filled histogram) or isotype control antibody (Catalog # IC002C, open histogram). View our protocol for Staining Membrane-associated Proteins.

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Preparation and Storage

Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Protect from light. Do not freeze.
  • 12 months from date of receipt, 2 to 8 °C as supplied.

Background: IL-3R alpha

IL-3 is a pleiotropic cytokine that can stimulate proliferation and differentiation of pluripotent hematopoietic stem cells as well as various lineage committed progenitors (1, 2). IL-3 exerts its activity through binding to a specific cell surface receptor known as IL-3 R. IL-3 R is a heterodimeric structure composed of a 70 kDa IL-3 R alpha subunit (CD123) and a 120-140 kDa IL-3 R beta subunit (CD131) (3, 4). IL-3 R alpha binds IL-3 with relatively low affinity. In the presence of IL-3 R beta, however, IL-3 R alpha has a much higher affinity for IL-3. It is not clear how signal transduction occurs following IL-3 binding. The IL-3 R alpha chain has a very short intracellular domain while the IL‑3 R beta chain has a very large cytoplasmic domain. The IL‑3 R beta chain is also shared by the receptors for IL-5 and GM-CSF. Cells known to express IL-3 receptors include hematopoietic progenitors, epithelial cells, double negative T cells, mast cells, basophils and blood monocytes (5).

References
  1. Moore, M.A.S. et al. (1991) Blood 72:944.
  2. Warren, D.J. et al. (1988) J. Immunol. 140:94.
  3. Plant M. et al. (1989) Nature 339:150.
  4. Budel, L.M. et al. (1990) Blood 75:1439.
  5. Schrader, J.W. et al. (1988) In Interleukin-3: The Panspecific hemopoietin (ed. J.W. Schrader), Academic Press, San Diego, CA.
Long Name
Interleukin 3 Receptor alpha
Entrez Gene IDs
3563 (Human); 16188 (Mouse); 102138639 (Cynomolgus Monkey)
Alternate Names
CD123 antigen; CD123; hIL3Ra; hIL-3Ra; IL-3 R alpha; IL-3 receptor subunit alpha; IL3R alpha; IL-3R alpha; IL-3R subunit alpha; IL3R; IL3RA; IL-3Ra; IL-3R-alpha; IL3RAY; IL3RX; IL3RY; interleukin 3 receptor, alpha (low affinity); interleukin-3 receptor subunit alpha; MGC34174

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Citations for Human IL-3R alpha/CD123 PerCP-conjugated Antibody

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

8 Citations: Showing 1 - 8
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  1. Dengue virus co-opts innate type 2 pathways to escape early control of viral replication
    Authors: Fonseka CL, Hardman CS, Woo J et al.
    Communications biology
  2. IL-6 effector function of group 2 innate lymphoid cells (ILC2) is NOD2 dependent
    Authors: Hardman CS, Chen YL, Salimi M et al.
    Science Immunology
  3. IL-6 effector function of group 2 innate lymphoid cells (ILC2) is NOD2 dependent
    Authors: Hardman CS, Chen YL, Salimi M et al.
    Science Immunology
  4. A role for IL-25 and IL-33-driven type-2 innate lymphoid cells in atopic dermatitis.
    Authors: Salimi M, Barlow J, Saunders S, Xue L, Gutowska-Owsiak D, Wang X, Huang L, Johnson D, Scanlon S, McKenzie A, Fallon P, Ogg G
    J Exp Med, 2013-12-09;210(13):2939-50.
    Species: Human
    Sample Types: Whole Cells
    Applications: Flow Cytometry
  5. Spontaneous atopic dermatitis is mediated by innate immunity, with the secondary lung inflammation of the atopic march requiring adaptive immunity
    Authors: Sean P. Saunders, Tara Moran, Achilleas Floudas, Felicity Wurlod, Agnieszka Kaszlikowska, Maryam Salimi et al.
    Journal of Allergy and Clinical Immunology
  6. Prostaglandin D2 activates group 2 innate lymphoid cells through chemoattractant receptor-homologous molecule expressed on TH2 cells.
    Authors: Xue L, Salimi M, Panse I, Mjosberg J, McKenzie A, Spits H, Klenerman P, Ogg G
    J Allergy Clin Immunol, 2013-12-31;133(4):1184-94.
  7. CD1a presentation of endogenous antigens by group 2 innate lymphoid cells
    Authors: Clare S. Hardman, Yi-Ling Chen, Maryam Salimi, Rachael Jarrett, David Johnson, Valtteri J. Järvinen et al.
    Science Immunology
  8. Group 2 innate lymphoid cells express functional NKp30 receptor inducing type 2 cytokine production1
    Authors: Maryam Salimi, Luzheng Xue, Helen Jolin, Clare Hardman, David J. Cousins, Andrew N. J. McKenzie et al.
    The Journal of Immunology

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