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Primary antibody against cd206

Manufactured by Abcam
Sourced in United States

The primary antibody against CD206 is a laboratory reagent used for the detection and study of the CD206 protein, also known as the macrophage mannose receptor. CD206 is a type I transmembrane protein that functions as an endocytic receptor, playing a role in the immune system. This antibody can be used in various immunological techniques, such as flow cytometry and immunohistochemistry, to identify and analyze cells expressing CD206.

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2 protocols using primary antibody against cd206

1

Nanoparticle-based Macrophage Modulation

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Soybean phosphatidylcholine (S100) was purchased from Lipoid GmbH (Ludwigshafen, Germany). Cholesterol, 1,2-distearoyl-sn-glycero-3-phosphoethanolamine- N-[amino(polyethylene glycol)-2000] (DSPE-PEG2000) and DSPE-PEG2000-N-hydroxysuccinimide ester (NHS) were purchased from A.V.T. Pharmaceutical Co., Ltd. (Shanghai, China). 4-Aminophenyl α-D-mannopyranoside was obtained from J&K Scientific Ltd. (Beijing, China). Coumarin-6 was purchased from Sigma-Aldrich (Saint Louis, MO, USA). 4′,6-Diamidino-2-phenylindole (DAPI) and LysoTracker Red were purchased from Beyotime (Haimen, Jiangsu, China). APC-CD86 and PE-CD206 were supplied by BioLegend (San Diego, CA, USA). The primary antibody against CD206 was obtained from Abcam (Cambridge, MA, USA). The primers of Arg1, Mgl2, and Ym1 were obtained from Invitrogen (Carlsbad, CA, USA). Recombinant murine interleukin-4 (IL-4) was supplied by PeproTech (Rocky Hill, NJ, USA). Dulbecco’s Modified Eagle’s Medium (DMEM) and fetal bovine serum (FBS) were purchased from Thermo Fisher Scientific Inc. (Waltham, MA, USA). Temozolomide capsules were purchased from Jiangsu Tasly Diyi Pharmaceutical Co., Ltd. (Huai’an, Jiangsu, China). All other organic reagents were of analytical grade and purchased from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China).
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2

Immunofluorescence Assay for CD206 Expression

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Cells were fixed in 4% paraformaldehyde (Biosesang, Seongnam, Korea) after washing with PBS (Invitrogen) containing 0.1% bovine serum albumin (BSA, Sigma Chemical Co., St. Louis, MO, USA). After 20 min on ice, the cells were washed with PBS/0.1% BSA twice for 10 min. Next, permeabilization solution containing 0.3% Triton X-100 (Sigma) was added to the cells. After 5 min, primary antibody against CD206 (Abcam) was dispensed at dilution of 1 : 200. After incubating overnight at 4°C, the fluorescence-labeled anti-rabbit IgG (Invitrogen) at dilution of 1 : 400 was used as the secondary antibody for 40 min at RT. After washing twice for 10 min, the cells were costained with DAPI (Sigma) for 5 min. The number of CD206-stained cells was counted and fluorescence images were obtained using a fluorescence microscope (Olympus IX71, Tokyo, Japan). The data are expressed as the mean ± SD of three independent experiments.
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