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Mouse M-CSF Quantikine ELISA Kit

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M-CSF is spiked at three known concentrations throughout the range of the assay and run to measure response of the spiked sample matrix. Plasma recovery is 103% compared to 84% for the top competitor. Cell culture ...read more

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Summary
Reactivity MuSpecies Glossary
Applications ELISA
Conjugate
HRP

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Mouse M-CSF Quantikine ELISA Kit Summary

Background
The Quantikine™ Mouse M-CSF Immunoassay is a 4.5 hour solid-phase ELISA designed to measure mouse M-CSF levels in cell culture supernates, serum, and plasma. It contains HEK293-expressed recombinant mouse M-CSF and antibodies raised against the recombinant factor. This immunoassay has been shown to accurately quantitate the recombinant mouse M-CSF. Results obtained using natural ...mouse M-CSF showed dose response curves that were parallel to the standard curves obtained using the Quantikine kit standards.  These results indicate that this kit can be used to determine relative mass values for natural mouse M-CSF.
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Specificity
Natural and recombinant mouse M-CSF.
Source
N/A
Inter-Assay
See PDF Datasheet for details
Intra-Assay
See PDF Datasheet for details
Spike Recovery
See PDF Datasheet for details
Sample Volume
See PDF Datasheet for details

Applications/Dilutions

Dilutions
  • ELISA
Application Notes
No significant interference observed with available related molecules.
Publications
Read Publications using MMC00B.

Packaging, Storage & Formulations

Storage
Store the unopened product at 2 - 8 °C. Do not use past expiration date.

Notes

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

Alternate Names for Mouse M-CSF Quantikine ELISA Kit

  • colony stimulating factor 1 (macrophage)
  • CSF1
  • CSF-1
  • Lanimostim
  • macrophage colony stimulating factor
  • macrophage colony-stimulating factor 1
  • MCSF
  • M-CSF
  • MCSFlanimostim
  • MGC31930

Background

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. M-CSF is also essential for the survival and proliferation of osteoclast progenitors. 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. M-CSF increases during pregnancy to support implantation and growth of the decidua and placenta. Sources of M-CSF include fibroblasts, activated macrophages, endometrial secretory epithelium, bone marrow stromal cells and activated endothelial cells. The M-CSF receptor (c-fms) transduces its pleotropic effects and mediates its endocytosis. M-CSF mRNAs of various sizes occur. Full length human M-CSF transcripts encode a 522 amino acid (aa) type I transmembrane (TM) protein with a 464 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. Shorter transcripts encode M-CSF that lack cleavage and PG sites and produce an N-glycosylated 68 kDa TM dimer and a slowly produced 44 kDa secreted dimer. 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. The first 223 aa of mature human M-CSF shares 88%, 86%, 81% and 74% aa identity with corresponding regions of dog, cow, mouse and rat M-CSF, respectively. Human M-CSF is active in the mouse, but mouse M-CSF is reported to be species-specific.

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Publications for M-CSF (MMC00B)(34)

We have publications tested in 1 confirmed species: Mouse.


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Mouse
(34)
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Showing Publications 1 - 10 of 34. Show All 34 Publications.
Publications using MMC00B Applications Species
Takacs, GP;Garcia, JS;Hodges, CA;Kreiger, CJ;Sherman, A;Harrison, JK; Glioma-derived M-CSF and IL-34 license M-MDSCs to suppress CD8+ T cells in a NOS-dependent manner bioRxiv : the preprint server for biology 2024-06-06 [PMID: 38895268] (Mouse) Mouse
Katoku-Kikyo, N;Lim, S;Yuan, C;Koroth, J;Nakagawa, Y;Bradley, EW;Kikyo, N; The circadian regulator PER1 promotes cell reprogramming by inhibiting inflammatory signaling from macrophages PLoS biology 2023-12-04 [PMID: 38048364] (Mouse) Mouse
YC Teh, MY Chooi, D Liu, I Kwok, GC Lai, L Ayub Ow Yo, M Ng, JLY Li, Y Tan, M Evrard, L Tan, KH Liong, K Leong, CC Goh, AYJ Chan, NB Shadan, CK Mantri, YY Hwang, H Cheng, T Cheng, W Yu, HL Tey, A Larbi, A St John, V Angeli, C Ruedl, B Lee, F Ginhoux, SL Chen, LG Ng, JL Ding, SZ Chong Transitional premonocytes emerge in the periphery for host defense against bacterial infections Science Advances, 2022-03-04;8(9):eabj4641. 2022-03-04 [PMID: 35245124] (Mouse) Mouse
JG Noel, SW Ramser, L Pitstick, JP Bonamer, B Mackenzie, KG Seu, TA Kalfa, JA Cancelas, JC Gardner M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling Scientific Reports, 2022-01-24;12(1):1235. 2022-01-24 [PMID: 35075211] (Mouse) Mouse
OJ Kwon, B Zhang, D Jia, L Zhang, X Wei, Z Zhou, D Liu, KT Huynh, K Zhang, Y Zhang, P Labhart, A Sboner, C Barbieri, MC Haffner, CJ Creighton, L Xin Elevated expression of the colony-stimulating factor 1 (CSF1) induces prostatic intraepithelial neoplasia dependent of epithelial-Gp130 Oncogene, 2022-01-08;0(0):. 2022-01-08 [PMID: 34999736] (Mouse) Mouse
W Li, X Zhang, C Zhang, J Yan, X Hou, S Du, C Zeng, W Zhao, B Deng, DW McComb, Y Zhang, DD Kang, J Li, WE Carson, Y Dong Biomimetic nanoparticles deliver mRNAs encoding costimulatory receptors and enhance T cell mediated cancer immunotherapy Nature Communications, 2021-12-14;12(1):7264. 2021-12-14 [PMID: 34907171] (Mouse) Mouse
AM La Rose, V Bazioti, JA Hoogerland, AF Svendsen, AG Groenen, M van Faasse, MGS Rutten, NJ Kloosterhu, B Dethmers-A, JH Nijland, G Mithieux, F Rajas, F Kuipers, MV Lukens, O Soehnlein, MH Oosterveer, M Westerterp Hepatocyte-specific glucose-6-phosphatase deficiency disturbs platelet aggregation and decreases blood monocytes upon fasting-induced hypoglycemia Molecular Metabolism, 2021-06-04;53(0):101265. 2021-06-04 [PMID: 34091064] (Mouse) Mouse
R Samain, A Brunel, T Douché, M Fanjul, S Cassant-So, J Rochotte, J Cros, C Neuzillet, J Raffenne, C Duluc, A Perraud, J Nigri, V Gigoux, I Bieche, M Ponzo, G Carpentier, I Cascone, R Tomasini, HA Schmid, M Mathonnet, R Nicolle, MP Bousquet, Y Martineau, S Pyronnet, C Jean, C Bousquet Pharmacological normalization of pancreatic cancer-associated fibroblast secretome impairs pro-metastatic cross-talk with macrophages: Stromal CSF-1 facilitates metastasis Cellular and Molecular Gastroenterology and Hepatology, 2021-01-20;0(0):. 2021-01-20 [PMID: 33482394] (Mouse) Mouse
M Song, OO Yeku, S Rafiq, T Purdon, X Dong, L Zhu, T Zhang, H Wang, Z Yu, J Mai, H Shen, B Nixon, M Li, RJ Brentjens, X Ma Tumor derived UBR5 promotes ovarian cancer growth and metastasis through inducing immunosuppressive macrophages Nature Communications, 2020-12-08;11(1):6298. 2020-12-08 [PMID: 33293516] (Mouse) Mouse
N Hagan, JL Kane, D Grover, L Woodworth, C Madore, J Saleh, J Sancho, J Liu, Y Li, J Proto, M Zelic, A Mahan, M Kothe, AA Scholte, M Fitzgerald, B Gisevius, A Haghikia, O Butovsky, D Ofengeim CSF1R signaling is a regulator of pathogenesis in progressive MS Cell Death Dis, 2020-10-23;11(10):904. 2020-10-23 [PMID: 33097690] (Mouse) Mouse
Show All 34 Publications.

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