Mouse M-CSF Antibody Summary
Lys33-Glu262 (predicted)
Accession # P07141
Applications
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
![Cell Proliferation Induced by M‑CSF and Neutralization by Mouse M‑CSF Antibody. Cell Proliferation Induced by M‑CSF and Neutralization by Mouse M‑CSF Antibody.](https://resources.rndsystems.com/images/datasheets/antibody/M-CSF_MAB4161_Block_Neutralize_2540.jpg)
Cell Proliferation Induced by M‑CSF and Neutralization by Mouse M‑CSF Antibody. Recombinant Mouse M-CSF (Catalog # 416-ML) stimulates proliferation in the M-NFS-60 mouse myelogenous luekemia lymphoblast cell line in a dose-dependent manner (orange line). Proliferation elicited by Recombinant Mouse M-CSF (10 ng/mL) is neutralized (green line) by increasing concentrations of Mouse M-CSF Monoclonal Antibody (Catalog # MAB4161). The ND50 is typically 3-12 µg/mL.
![Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence](https://resources.rndsystems.com/images/datasheets/mab4161_mouse-m-csf-mab-clone-131614-4120241252126.jpg)
Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence Injury-induced SSEA-1 positive cells were regulated by topical application of M-CSF or M-CSF neutralizing antibody.Skin wounds in mice were treated by either PBS control (top panels) or topical application of recombinant M-CSF protein (middle panels) or topical application of M-CSF neutralizing antibody for 6 days. This figure showed a representative skin section from 6 wounds in each group, stained with SSEA-1 (red color). DAPI (blue) was used for cell nucleus staining. Scale bars, 100 μm. Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/srep28979), licensed under a CC-BY license. Not internally tested by R&D Systems.
![Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence](https://resources.rndsystems.com/images/datasheets/mab4161_mouse-m-csf-mab-clone-131614-41202412511314.jpg)
Detection of Mouse M-CSF by Immunocytochemistry/Immunofluorescence SSEA-1 positive cells are also SSEA-3 positive and express M-CSF receptor.(A) Injured skin sections were stained with SSEA-1 (red color) and SSEA-3 (green color) antibodies. IgG was used for a negative staining control. DAPI (blue) was used for cell nucleus staining. Scale bars, 50 μm. (B) Injured skin sections were stained with SSEA-1 (green color) and M-CSF receptor (red color) antibodies. DAPI (blue) was used for cell nucleus staining. Scale bars, 50 μm. Image collected and cropped by CiteAb from the following publication (https://www.nature.com/articles/srep28979), licensed under a CC-BY license. Not internally tested by R&D Systems.
Preparation and 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.
Background: M-CSF
M-CSF, also known as CSF-1, is a four-alpha -helical-bundle cytokine that is the primary regulator of macrophage survival, proliferation and differentiation (1-3). M-CSF is also essential for the survival and proliferation of osteoclast progenitors (1, 4). M-CSF also primes and enhances macrophage killing of tumor cells and microorganisms, regulates the release of cytokines and other inflammatory modulators from macrophages, and stimulates pinocytosis (2, 3). M-CSF increases during pregnancy to support implantation and growth of the decidua and placenta (5). Sources of M-CSF include fibroblasts, activated macrophages, endometrial secretory epithelium, bone marrow stromal cells, and activated endothelial cells (1-5). The M-CSF receptor (c-fms) transduces its pleotropic effects and mediates its endocytosis. M-CSF mRNAs of various sizes occur (3-9). Full length mouse M-CSF transcripts encode a 520 amino acid (aa) type I transmembrane (TM) protein with a 462 aa extracellular region, a 21 aa TM domain, and a 37 aa cytoplasmic tail that forms a 140 kDa covalent dimer. Differential processing produces two proteolytically cleaved, secreted dimers. One is an N- and O-glycosylated 86 kDa dimer, while the other is modified by both glycosylation and chondroitin-sulfate proteoglycan (PG) to generate a 200 kDa subunit. Although PG-modified M-CSF can circulate, it may be immobilized by attachment to type V collagen (8). Shorter transcripts encode M-CSF that lacks cleavage and PG sites and produces an N-glycosylated 68 kDa TM dimer and a slowly produced 44 kDa secreted dimer (7). Although forms may vary in activity and half-life, all contain the N-terminal 150 aa portion that is necessary and sufficient for interaction with the M-CSF receptor (10, 11). The first 229 aa of mature mouse M-CSF shares 87%, 83%, 82%, and 81% aa identity with corresponding regions of rat, dog, cow, and human M-CSF, respectively (12, 13). Human M-CSF is active in the mouse, but mouse M-CSF is reported to be species-specific.
- Pixley, F.J. and E.R. Stanley (2004) Trends Cell Biol. 14:628.
- Chitu, V. and E.R. Stanley (2006) Curr. Opin. Immunol. 18:39.
- Fixe, P. and V. Praloran (1997) Eur. Cytokine Netw. 8:125.
- Ryan, G.R. et al. (2001) Blood 98:74.
- Makrigiannakis, A. et al. (2006) Trends Endocrinol. Metab. 17:178.
- Nandi, S. et al. (2006) Blood 107:786.
- Rettenmier, C.W. and M.F. Roussel (1988) Mol. Cell Biol. 8:5026.
- Suzu, S. et al. (1992) J. Biol. Chem. 267:16812.
- Manos, M.M. (1988) Mol. Cell. Biol. 8:5035.
- Koths, K. (1997) Mol. Reprod. Dev. 46:31.
- Jang, M-H. et al. (2006) J. Immunol. 177:4055.
- DeLamarter, J.F. et al. (1987) Nucleic Acids Res. 15:2389.
- Ladner, M.B. et al. (1988) Proc. Natl. Acad. Sci. USA 85:6706.
Product Datasheets
Citations for Mouse M-CSF 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.
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Citations: Showing 1 - 7
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Enteric Glia Modulate Macrophage Phenotype and Visceral Sensitivity following Inflammation
Authors: V Grubiši?, JL McClain, DE Fried, I Grants, P Rajasekhar, E Csizmadia, OA Ajijola, RE Watson, DP Poole, SC Robson, FL Christofi, BD Gulbransen
Cell Rep, 2020-09-08;32(10):108100.
Species: Mouse
Sample Types: In situ
Applications: Activation -
Bone-derived Nestin-positive mesenchymal stem cells improve cardiac function via recruiting cardiac endothelial cells after myocardial infarction
Authors: D Lu, Y Liao, SH Zhu, QC Chen, DM Xie, JJ Liao, X Feng, MH Jiang, W He
Stem Cell Res Ther, 2019-04-27;10(1):127.
Species: N/A
Sample Types: Recombinant Protein
Applications: Western Blot -
Interleukin-18 Amplifies Macrophage Polarization and Morphological Alteration, Leading to Excessive Angiogenesis
Authors: T Kobori, S Hamasaki, A Kitaura, Y Yamazaki, T Nishinaka, A Niwa, S Nakao, H Wake, S Mori, T Yoshino, M Nishibori, H Takahashi
Front Immunol, 2018-03-06;9(0):334.
Species: Mouse
Sample Types: Cell Lysates, Whole Cells
Applications: Neutralization, Western Blot -
An inflammatory gene signature distinguishes neurofibroma Schwann cells and macrophages from cells in the normal peripheral nervous system
Authors: K Choi, K Komurov, JS Fletcher, E Jousma, JA Cancelas, J Wu, N Ratner
Sci Rep, 2017-03-03;7(0):43315.
Species: Mouse
Sample Types: Whole Cells
Applications: Neutralization -
CSF-1 receptor-mediated differentiation of a new type of monocytic cell with B cell-stimulating activity: its selective dependence on IL-34.
Authors: Yamane F, Nishikawa Y, Matsui K, Asakura M, Iwasaki E, Watanabe K, Tanimoto H, Sano H, Fujiwara Y, Stanley E, Kanayama N, Mabbott N, Magari M, Ohmori H
J Leukoc Biol, 2013-09-19;95(1):19-31.
Species: Mouse
Sample Types: Cell Lysates
Applications: Western Blot -
Colony-stimulating factor 1 receptor (CSF1R) signaling in injured neurons facilitates protection and survival.
Authors: Luo, Jian, Elwood, Fiona, Britschgi, Markus, Villeda, Saul, Zhang, Hui, Ding, Zhaoqing, Zhu, Liyin, Alabsi, Haitham, Getachew, Ruth, Narasimhan, Ramya, Wabl, Rafael, Fainberg, Nina, James, Michelle, Wong, Gordon, Relton, Jane, Gambhir, Sanjiv S, Pollard, Jeffrey, Wyss-Coray, Tony
J Exp Med, 2013-01-07;210(1):157-72.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Osteoblasts support B-lymphocyte commitment and differentiation from hematopoietic stem cells.
Authors: Zhu J, Garrett R, Jung Y, Zhang Y, Kim N, Wang J, Joe GJ, Hexner E, Choi Y, Taichman RS, Emerson SG
Blood, 2007-01-16;109(9):3706-12.
Species: Mouse
Sample Types: Whole Cells
Applications: Neutralization
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