Recombinant Cynomolgus Monkey IL-3R alpha Fc Protein, CF

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When Recombinant Cynomolgus Monkey IL-3R alpha Fc Chimera (Catalog #10597-R3) is present at 1 µg/mL (100 µg/mL), the concentration of Recombinant Human IL-3 Protein (203-IL) that produces 50% optimal binding response ...read more
2 μg/lane of Recombinant Cynomolgus Monkey IL-3R alpha Fc Chimera (Catalog # 10597-R3) was resolved with SDS-PAGE under reducing (R) and non-reducing (NR) conditions and visualized by Coomassie® Blue staining, ...read more

Product Details

Summary
Reactivity Pm-CmSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Cynomolgus Monkey IL-3R alpha Fc Protein, CF Summary

Details of Functionality
Measured by its binding ability in a functional ELISA. When Recombinant Cynomolgus Monkey IL-3R alpha Fc Chimera prootein (Catalog #10597-R3) is represent at 1 µg/mL (100 µg/mL), The concentration of Recombinant Human IL-3 Protein (Catalog # 203-IL) that produces 50% optimal binding response is found to be 8-40 ng/mL.
Source
Chinese Hamster Ovary cell line, CHO-derived cynomolgus monkey IL-3R alpha protein
Cynomolgus Monkey IL-3R alpha
(Arg18-Arg305)
Accession # EHH61867.1
IEGRMD Human IgG1
(Pro100-Lys330)
N-terminusC-terminus
Accession #
N-terminal Sequence
Arg18
Structure / Form
Disulfide-linked homodimer
Protein/Peptide Type
Recombinant Proteins
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Note
<0.10 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
60 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
85-100 kDa, under reducing conditions

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in PBS.
Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Reconstitution Instructions
Reconstitute at 200μg/mL in PBS.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Cynomolgus Monkey IL-3R alpha Fc Protein, CF

  • 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

Background

IL-3 receptor chain alpha (IL‑3Ra) also known as CD123, is a member of the type 1 cytokine receptor family of proteins expressed mainly by activated T cells or mast cells (1-3). IL-3Ra is a 60-70 kDa receptor component that binds IL-3 with low affinity and forms one-half of the IL-3 receptor complex. IL-3Ra associates with the 130-140 kDa non-ligand binding IL-3Rb for high-affinity binding to IL-3 to form the heterodimeric receptor complex (4). IL-3Ra consists of an extracellular domain (ECD) with an N-terminal Ig-like C2-type domain and a cytokine-binding domain containing two fibronectin type-III domains with a WSXWS motif, a helical transmembrane segment and a cytoplasmic domain (3). Within the mature ECD, cynomolgus IL-3Ra shares 85% amino acid sequence identity with human IL-3Ra. An isoform lacking the N-terminal domain of ECD has been identified in mouse and human (5, 6). IL‑3 stimulates the proliferation and differentiation of hemopoietic cells including the pluripotent hematopoietic stem cells as well as various lineage‑committed cells (7). IL-3Ra is expressed on multiple cell types, including endothelial cells, monocytes, eosinophils, basophils plus mast cells, and plasmacytoid CD4+ T cells (8). IL-3Ra is over-expressed by Acute myeloid leukemia and this is associated with a poor prognosis in AML (9).
  1. Broughton, S.E. et al. (2012) Immunol. Rev. 250:277.
  2. Langer, J.A. et al. (2004) Cytokine Growth Factor Rev. 15:33.
  3. Broughton, S.E. et al. (2014) Acta Crystallogr F Struc Biol Commun. 70:358.
  4. Broughton, S.E. et al. (2014) Cell Reports. 8:410.
  5. Chen, J. et al. (2009) J. Biol. Chem. 284:5763.
  6. Hamming, O.J. et al. (2012) J Biol Chem. 287:9454.
  7. Ogorochi, T. and A. Miyajima (1994) in Guidebook to Cytokines and Their Receptors, N.A. Nicola, ed. Oxford University, New York p. 40.
  8. Michalska, A. et al. (2020) Postepy Dermatol Alergol. 37:299.
  9. Testa, U. et al. (2002) Blood 100:2980.

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