M-CSF receptor, the product of the c-fms proto-oncogene, is a member of the type III subfamily of receptor tyrosine kinases that also includes receptors for SCF and PDGF. These receptors each contain five immunoglobulin-like domains in their extracellular domain (ECD) and a split kinase domain in their intracellular region (1-4). M-CSF receptor is expressed primarily on cells of the monocyte/macrophage lineage, dendritic cells, stem cells and in the developing placenta (1). Human M-CSF receptor cDNA encodes a 972 amino acid (aa) type I membrane protein with a 19 aa signal peptide, a 493 aa extracellular region containing the ligand-binding domain, a 25 aa transmembrane domain, and a 435 aa cytoplasmic domain. The human M-CSF R ECD shares 60%, 64%, 72%, 75%, 75%, and 76% aa identity with mouse, rat, bovine, canine, feline, and equine M-CSF R, respectively. Activators of protein kinase C induce TACE/ADAM17 cleavage of the M-CSF receptor, releasing the functional ligand-binding extracellular domain (5). M-CSF binding induces receptor homodimerization, resulting in transphosphorylation of specific cytoplasmic tyrosine residues and signal transduction (6). The intracellular domain of activated M-CSF R binds more than 150 proteins that affect cell proliferation, survival, differentiation and cytoskeletal reorganization. Among these, PI3Kinase, P42/44 ERK and c-Cbl are key transducers of M-CSF R signals (3, 4). M-CSF R engagement is continuously required for macrophage survival and regulates lineage decisions and maturation of monocytes, macrophages, osteoclasts and DC (3, 4). M-CSF R and integrin alpha v beta 3 share signaling pathways during osteoclastogenesis and deletion of either causes osteopetrosis (7, 8). In the brain, microglia expressing increased
M‑CSF R are concentrated with Alzheimers a beta peptide, but their role in pathogenesis is unclear (9, 10).
Human M-CSF R/CD115 Antibody
R&D Systems | Catalog # AF329
Scientific images may be resized, cropped, or adjusted for brightness or contrast for presentation purposes. These updates are limited to presentation and do not affect the underlying scientific interpretation of the data. Where available, additional source data may be provided upon request.
Key Product Details
Species Reactivity
Validated:
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Applications
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Label
Antibody Source
Product Specifications
Immunogen
Ile20-Glu512
Accession # CAA27300
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human M-CSF R/CD115 Antibody
Detection of M-CSF R/CD115 in THP-1 cells by Flow Cytometry
THP-1 cells were stained with Goat Anti-Human M-CSF R/CD115 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF329, filled histogram) or isotype control antibody (Catalog # AB-108-C, open histogram) followed by Allophycocyanin-conjugated Anti-Goat IgG Secondary Antibody (Catalog # F0108). View our protocol for Staining Membrane-associated Proteins.Detection of M-CSF R/CD115 by Western Blot
MTX modulates the expression of MAF, MAFB, and CSF1R in M-MØ. a Schematic representation of the experiment. Monocytes were differentiated to macrophages in the presence of M-CSF for 7 days. Five micromolar MTX was added once on monocytes [MTX-M-MØ], or on 2 days (MTX-M-MØ [d2]) or 5 days (MTX-M-MØ [d5]) after the beginning of the differentiation process with M-CSF. RNA or protein levels were determined at day 7. b Relative mRNA expression levels of the indicated genes as determined by qRT-PCR on M-MØ, MTX-M-MØ, MTX-M-MØ (d2), and MTX-M-MØ (d5). Mean ± SEM of three independent donors are shown. Groups were compared by applying one-way ANOVA (with Tukey's post hoc test, *p < 0.05). c Scatter plot of RNAseq results showing upregulated expression gene changes in MTX-M-MØ versus MTX-M-MØ (d5). d Venn diagram comparing the genes differentially expressed by MTX in MTX-M-MØ with the genes significantly altered by MTX in and MTX-M-MØ (d5). e Allogeneic CD3+ T-lymphocyte proliferation promoted by M-MØ and MTX-M-MØ (d5). Shown are two experiments using independent preparations of M-MØ. Mean ± SEM of six replicates performed in each experiment are shown (**p < 0.01). f Immunoblot analysis of CSF1R, MAFB, and MAF by M-MØ and MTX-M-MØ (d5). GAPDH protein levels were determined as protein loading control. g Immunoblot analysis of CSF1R and MAFB by M-MØ, MTX-M-MØ (d5), or MTX-M-MØ (d5) exposed to FA. Tubulin protein levels were determined as protein loading control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36380627), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of M-CSF R/CD115 by Western Blot
MTX modulates the expression of MAF, MAFB, and CSF1R in M-MØ. a Schematic representation of the experiment. Monocytes were differentiated to macrophages in the presence of M-CSF for 7 days. Five micromolar MTX was added once on monocytes [MTX-M-MØ], or on 2 days (MTX-M-MØ [d2]) or 5 days (MTX-M-MØ [d5]) after the beginning of the differentiation process with M-CSF. RNA or protein levels were determined at day 7. b Relative mRNA expression levels of the indicated genes as determined by qRT-PCR on M-MØ, MTX-M-MØ, MTX-M-MØ (d2), and MTX-M-MØ (d5). Mean ± SEM of three independent donors are shown. Groups were compared by applying one-way ANOVA (with Tukey's post hoc test, *p < 0.05). c Scatter plot of RNAseq results showing upregulated expression gene changes in MTX-M-MØ versus MTX-M-MØ (d5). d Venn diagram comparing the genes differentially expressed by MTX in MTX-M-MØ with the genes significantly altered by MTX in and MTX-M-MØ (d5). e Allogeneic CD3+ T-lymphocyte proliferation promoted by M-MØ and MTX-M-MØ (d5). Shown are two experiments using independent preparations of M-MØ. Mean ± SEM of six replicates performed in each experiment are shown (**p < 0.01). f Immunoblot analysis of CSF1R, MAFB, and MAF by M-MØ and MTX-M-MØ (d5). GAPDH protein levels were determined as protein loading control. g Immunoblot analysis of CSF1R and MAFB by M-MØ, MTX-M-MØ (d5), or MTX-M-MØ (d5) exposed to FA. Tubulin protein levels were determined as protein loading control. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/36380627), licensed under a CC-BY license. Not internally tested by R&D Systems.Human M-CSF R / CD115 ELISA Standard Curve
Recombinant Human M-CSF R/CD115 Fc Chimera (Catalog # 329-MR) was serially diluted and captured by Mouse Anti-Human M-CSF R/CD115 Monoclonal Antibody (Catalog # MAB3292) coated on a Clear Polystyrene Microplate (Catalog # DY990). Goat Anti-Human M-CSF R/CD115 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF329) was biotinylated and incubated with the protein captured on the plate. Detection of the standard curve was achieved by incubating Streptavidin-HRP (Catalog # DY998)Applications for Human M-CSF R/CD115 Antibody
CyTOF-ready
Flow Cytometry
Sample: THP-1 human acute monocytic leukemia cell line
Western Blot
Sample: Recombinant Human M-CSF R/CD115 Fc Chimera (Catalog # 329-MR)
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: M-CSF R/CD115
References
- deParseval, N. et al. (1993) Nucleic Acids Res. 21:750.
- Rothwell, V.M. and L.R. Rohrschneider (1987) Oncogene Res. 1:311.
- Chitu, V. and E.R. Stanley (2006) Curr. Opin. Immunol. 18:39.
- Ross, F.P. and S.L. Teitelbaum (2005) Immunol. Rev. 208:88.
- Rovida, E. et al. (2001) J. Immunol. 166:1583.
- Yeung, Y. et al. (1998) J. Biol. Chem. 273:17128.
- Dai, X. et al. (2002) Blood 99:111.
- Faccio, R. et al. (2003) J. Clin. Invest. 111:749.
- Li, M. et al. (2004) J. Neurochem. 91:623.
- Mitrasinovic, O.M. et al. (2005) J. Neurosci. 25:4442.
Long Name
Alternate Names
Gene Symbol
UniProt
Additional M-CSF R/CD115 Products
Product Documents for Human M-CSF R/CD115 Antibody
Certificate of Analysis
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Product Specific Notices for Human M-CSF R/CD115 Antibody
For research use only
Citations for Human M-CSF R/CD115 Antibody
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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- Western Blot Conditions
- Western Blot Protocol
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- Western Blot Troubleshooting Guide
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