F4/80, Mouse Antibody from MILTENYI BIOTEC B.V. & Co. KG

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Antigenic SpecificityF4/80, Mouse
CloneREA126
Host SpeciesRecombinant Human
Reactive Speciesmouse
IsotypeIgG1
FormatPE-Vio 770 conjugate
Size150 µg in 1 mL
Concentration1:50
ApplicationsFlow cytometry
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DescriptionF4/80 Antibody, anti-mouse, PE-Vio® 770, REAfinity™. Clone REA126 recognizes F4/80, a member of epidermal growth factor (EGF)-transmembrane 7 (TM7) family. F4/80 is considered as one of the most specific cell-surface markers for murine macrophages. F4/80 is a seven-span transmembrane molecule with a large extracellular, multiple EGF module-containing domain. Constitutive and high expression of F4/80 is found on most resident tissue macrophages, including the spleen, microglia in the brain, Kupffer's cells in the liver, and Langerhans cells in the skin. In addition, the expression of F4/80 can also be regulated depending on the physiological status of the cell. F4/80 molecule is required for the differentiation of antigen-specific CD8+ Tregs and is involved in inducing peripheral immune tolerance. No specific ligand for F4/80 has been reported so far. | Additional information: Clone REA126 displays negligible binding to Fc receptors. |
Immunogenn/a
Other NamesADGRE1, DD7A5-7, EGF-TM7, EMR1, Gpf480, Ly71, TM7LN3
Gene, Accession #Gene ID: 13733
Catalog #130-118-320
Price$450
Order / More InfoF4/80, Mouse Antibody from MILTENYI BIOTEC B.V. & Co. KG
Product Specific ReferencesLin, H.-H. et al. (2005) The macrophage F4/80 receptor is required for the induction of antigen-specific efferent regulatory T cells in peripheral tolerance. J. Exp. Med. 201: 1615-1625. | Gordon, S. et al. (2011) F4/80 and the related adhesion-GPCRs. Eur. J. Immunol. 41 (9): 2472-2476. | Kortlever, R. M. et al. (2017) Myc Cooperates with Ras by Programming Inflammation and Immune Suppression. Cell 171 (6): 1301-1315. | Hume, D. A. et al. (1984) The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80: macrophages of bone and associated connective tissue. J. Cell. Sci. 66: 189-194. | Gu, C. et al. (2018) EcoHIV infection of mice establishes latent viral reservoirs in T cells and active viral reservoirs in macrophages that are sufficient for induction of neurocognitive impairment. PLoS Pathog. 14 (6): . | Siegmund, D. et al. (2016) Activation of TNFR2 sensitizes macrophages for TNFR1-mediated necroptosis. Cell Death Dis 7 (9): e2375. | Siegmund, D. et al. (2018) TNFR2 unlocks a RIPK1 kinase activity-dependent mode of proinflammatory TNFR1 signaling. Cell Death Dis 9 (9): . | Lee, H. et al. (2017) Kinetics of corneal antigen presenting cells in experimental dry eye disease. BMJ Open Ophthalmol 1 (1): . | Jia, J. et al. (2018) Cholesterol metabolism promotes B-cell positioning during immune pathogenesis of chronic obstructive pulmonary disease. EMBO Mol. Med. 10 (5): .
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
Friedrich-Ebert-Straße 68
51429 Bergisch Gladbach GERMANY
P: +49 2204 8306-0
F: +49 2204 85197

macs@miltenyibiotec.de

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