Recombinant Human M-CSF (carrier-free)

Pricing & Availability
Regulatory Status
RUO
Other Names
CSF1, CSF-1, MCSF
M-CSF_Human_021512
M-NFS-60 cell proliferation induced by human M-CSF.
  • M-CSF_Human_021512
    M-NFS-60 cell proliferation induced by human M-CSF.
  • Recombinant_Human_MCSF_CF_012022
    Recombinant human M-CSF induces the proliferation of mouse M-NFS60 cell line in a dose dependent manner. BioLegend’s protein was compared side-by-side to the leading competitor’s equivalent product.
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574802 10 µg $112.00
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574804 25 µg $206.00
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574806 100 µg $645.00
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574808 500 µg $1758.00
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Description

M-CSF was first characterized as a glycoprotein that induces monocyte and macrophage colony formation from precursors in murine bone marrow cultures. M-CSF is constitutively present at biologically active concentrations in human serum. It binds CD14+ monocytes and promotes the survival/proliferation of human peripheral blood monocytes. In addition, M-CSF enhances inducible monocyte functions including phagocytic activity, microbial killing, cytotoxicity for tumor cells as well as synthesis of inflammatory cytokines such as IL-1, TNFα, and INFγ in monocytes. M-CSF induces RANKL production in mature human osteoclasts; consequently, M-CSF is a potent stimulator of mature osteoclast resorbing activity. Also, M-CSF induces VEGF in human monocytes in human tumors; high levels of M-CSF, mononuclear phagocytes, and VEGF are associated with poor prognosis in patients with cancer. High levels of M-CSF have been associated with different pathologies such as pulmonary fibrosis and atherosclerosis. M-CSF binds to its receptor M-CSFR, and this receptor is shared by a second ligand, IL-34. Human M-CSF and IL-34 exhibit cross-species specificity – both bind to human and mouse M-CSF receptors.

Technical data sheet

Product Details

Source
Human M-CSF, amino acids Glu33-Ser190 (Accession# NM_172212.2) was expressed in 293E cells.
Molecular Mass
The 179 amino acid recombinant protein has a predicted molecular mass of approximately 20.6 kD. The DTT-reduced and non-reduced protein migrate at approximately 25- 35 kD and 55-70 kD respectively by SDS-PAGE. The N-terminal contains a His9-(SGGG)2-IEGR-tag.
Purity
>98%, as determined by Coomassie stained SDS-PAGE.
Formulation
0.22 µm filtered protein solution is in PBS.
Endotoxin Level
Less than 0.01 ng per µg cytokine as determined by the LAL method.
Concentration
10 and 25 µg sizes are bottled at 200 µg/mL. 100 µg size and larger sizes are lot-specific and bottled at the concentration indicated on the vial. To obtain lot-specific concentration and expiration, please enter the lot number in our Certificate of Analysis online tool.
Storage & Handling
Unopened vial can be stored between 2°C and 8°C for up to 2 weeks, at -20°C for up to six months, or at -70°C or colder until the expiration date. For maximum results, quick spin vial prior to opening. The protein can be aliquoted and stored at -20°C or colder. Stock solutions can also be prepared at 50 - 100 µg/mL in appropriate sterile buffer, carrier protein such as 0.2 - 1% BSA or HSA can be added when preparing the stock solution. Aliquots can be stored between 2°C and 8°C for up to one week and stored at -20°C or colder for up to 3 months. Avoid repeated freeze/thaw cycles.
Activity
ED50 =0.5 - 2 ng/ml, corresponding to a specific activity of 0.5 - 2 x 106 units/mg, as determined by M-NFS60 cell proliferation induced by human M-CSF in a dose dependent manner.
Application

Bioassay

Application Notes

BioLegend carrier-free recombinant proteins provided in liquid format are shipped on blue-ice. Our comparison testing data indicates that when handled and stored as recommended, the liquid format has equal or better stability and shelf-life compared to commercially available lyophilized proteins after reconstitution. Our liquid proteins are verified in-house to maintain activity after shipping on blue ice and are backed by our 100% satisfaction guarantee. If you have any concerns, contact us at tech@biolegend.com.

Application References

(PubMed link indicates BioLegend citation)
  1. Lou J, et al. 2014. J Cell Sci. 127:5228. PubMed
Product Citations
  1. Xiang J, et al. 2022. J Virol. 96:e0005722. PubMed
  2. Mirji G, et al. 2022. Sci Immunol. 7:eabn0704. PubMed
  3. Hong Y, et al. 2023. iScience. 26:106267. PubMed
  4. Nilsson A, et al. 2022. Nat Commun. 13:3069. PubMed
  5. Tsuchiya N, et al. 2020. Cell Reports. 29(1):162-175.e9.. PubMed
  6. Goel PN, et al. 2019. Biochem Biophys Res Commun. 515:538. PubMed
  7. Nenasheva T, et al. 2020. Front Immunol. 1.163888889. PubMed
  8. Sandstrom TS, et al. 2021. J Virol. 95:. PubMed
  9. Chen X, et al. 2021. Theranostics. 11:3392. PubMed
  10. Cordido A, et al. 2021. J Am Soc Nephrol. 32:1913. PubMed
  11. Walter F, et al. 2020. PLoS One. 15:e0239369. PubMed
  12. Trapecar M, et al. 2021. Sci Adv. 7:00. PubMed
  13. Cassetta L et al. 2019. Cancer Cell. 35(4):588-602 . PubMed
  14. Anantpadma M, et al. 2016. Antimicrob Agents Chemother. 60: 4471 - 4481. PubMed
  15. Zhai K, et al. 2021. Nat Cancer. 2:1136. PubMed
  16. Lin H, et al. 2020. Small. 16:e2002194. PubMed
  17. Yamada KJ, et al. 2020. PLoS Pathog. 16:e1008354. PubMed
  18. Thi Tran U, et al. 2019. Commun Biol. 2:2. PubMed
  19. Heath O, et al. 2021. Cancer Immunol Res. 9:665. PubMed
  20. Yamaguchi Y, et al. 2022. J Immunother Cancer. 10:. PubMed
  21. Dahal S, et al. 2022. Retrovirology. 19:18. PubMed
  22. Stephens WZ, et al. 2021. Cell Rep. 37:109916. PubMed
  23. Heim CE, et al. 2020. Nature Microbiology. 5(10):1271-1284. PubMed
  24. Brasil da Costa FH, et al. 2020. PLoS One. 15:e0230354. PubMed
  25. Lu Y, et al. 2020. Immunity. 52:782. PubMed
  26. Miyamoto T, et al. 2021. Cancer Immunol Res. Online ahead of print. PubMed
  27. Virtakoivu R, et al. 2021. Clin Cancer Res. 27:4205. PubMed
  28. Lou J, et al. 2014. J Cell Sci. 127:5228. PubMed
  29. Rexach JE, et al. 2020. Cell Rep. 33:108398. PubMed
  30. Kuniholm J, et al. 2021. PLoS Pathog. 17:e1009982. PubMed
  31. Nijaguna M, et al. 2015. J Biol Chem. 290: 23401-23415. PubMed
  32. Lecker LSM, et al. 2021. Cancer Res. 81:5706. PubMed
  33. Yang F, et al. 2021. Nat Commun. 12:3424. PubMed

Antigen Details

Structure
Disulfide-linked glycosylated homodimer
Interaction
Monocytes, macrophages, mononuclear phagocyte precursors, microglia, proliferating smooth muscle cells, umbilical vein endothelial cells, and breast cancer cell lines.
Ligand/Receptor
M-CSFR or CSF1R (CD115)
Cell Type
Embryonic Stem Cells, Hematopoietic stem and progenitors
Biology Area
Cell Biology, Cell Proliferation and Viability, Immunology, Stem Cells
Molecular Family
Cytokines/Chemokines, Growth Factors
Antigen References

1. Kawasaki ES, et al. 1985. Science 230:291.
2. Wei S, et al. 2010. J. Leukoc. Biol. 88:495.
3. Hodge JM, et al. 2011. PloS One 6:e21462.
4. Morandi A, et al. 2011. PloS One 6:e27450.
5. Erblich B, et al. 2011. PloS One 6:e26317.
6. MacDonald KP, et al. 2010. Blood 116:3955.

Gene ID
1435 View all products for this Gene ID
UniProt
View information about M-CSF on UniProt.org
Go To Top Version: 5    Revision Date: 09/27/2017

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