Review

cd163 protein (Beyotime)

Beyotime manufactures this product

About

News

Press Release

Team

Advisors

Partners

Contact

Bioz Stars

Bioz vStars

Buy from Supplier

Structured Review

Beyotime cd163 protein

Compound A inhibited macrophages for polarized M2 phenotype in IL-4-stimulated RAW264.7 cells. ( a ) After treating with IL-4 (20 ng/mL) for 24 h, the expression and phosphorylation of PKC δ, ERK, and STAT6 were detected 0–60 min after compound A (10 μmol·L −1 ) treatment. Statistical significance was represented as follows: * p < 0.05, *** p < 0.001 versus 0 min group. ( b ) The expression and phosphorylation of STAT3 and STAT6 were detected 24 h after compound A treatment. Statistical significance was represented as follows: ### p < 0.001 versus C group; *** p < 0.001 versus IL-4 group. ( c ) The expression of TGF-β, <t>CD163,</t> CD206, ARG-1 was detected. ( d ) Representative images of immunofluorescence staining of CD206 (green) and DAPI (blue) of IL-4-induced RAW264.7 cells. Statistical significance was represented as follows: # p < 0.05, ## p < 0.01, ### p < 0.001 versus C group; ** p < 0.01, *** p < 0.001 versus IL-4 group.

Cd163 Protein, supplied by Beyotime, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd163 protein/product/Beyotime
Average 90 stars, based on 1 article reviews

cd163 protein - by Bioz Stars, 2026-03

90/100 stars

Images

1) Product Images from "An Ingenane-Type Diterpene from Euphorbia kansui Promoted Cell Apoptosis and Macrophage Polarization via the Regulation of PKC Signaling Pathways"

Article Title: An Ingenane-Type Diterpene from Euphorbia kansui Promoted Cell Apoptosis and Macrophage Polarization via the Regulation of PKC Signaling Pathways

Journal: International Journal of Molecular Sciences

doi: 10.3390/ijms251810123

Figure Legend Snippet: Compound A inhibited macrophages for polarized M2 phenotype in IL-4-stimulated RAW264.7 cells. ( a ) After treating with IL-4 (20 ng/mL) for 24 h, the expression and phosphorylation of PKC δ, ERK, and STAT6 were detected 0–60 min after compound A (10 μmol·L −1 ) treatment. Statistical significance was represented as follows: * p < 0.05, *** p < 0.001 versus 0 min group. ( b ) The expression and phosphorylation of STAT3 and STAT6 were detected 24 h after compound A treatment. Statistical significance was represented as follows: ### p < 0.001 versus C group; *** p < 0.001 versus IL-4 group. ( c ) The expression of TGF-β, CD163, CD206, ARG-1 was detected. ( d ) Representative images of immunofluorescence staining of CD206 (green) and DAPI (blue) of IL-4-induced RAW264.7 cells. Statistical significance was represented as follows: # p < 0.05, ## p < 0.01, ### p < 0.001 versus C group; ** p < 0.01, *** p < 0.001 versus IL-4 group.

Techniques Used: Expressing, Phospho-proteomics, Immunofluorescence, Staining

Image Search Results

Increased macrophages and elevated CD163 expression in macrophages in the ovary and uterus of PCOS mice. ( a ) Representative immunofluorescence images of CD163 and F4/80 in ovaries and uteri of control and PCOS mice (scale bar = 100 μm). ( b ) Quantification of CD163 + , F4/80 + , and F4/80 + CD163 + cell proportions in the ovaries and uteri of control and PCOS mice. * p < 0.05, ** p < 0.01, ns: p > 0.05.

Journal: Journal of Inflammation Research

Article Title: Increased CD163+ Macrophage Activation and High Expression of CD163 Promote Granulosa Cell Apoptosis in Polycystic Ovary Syndrome

doi: 10.2147/JIR.S532920

Figure Lengend Snippet: Increased macrophages and elevated CD163 expression in macrophages in the ovary and uterus of PCOS mice. ( a ) Representative immunofluorescence images of CD163 and F4/80 in ovaries and uteri of control and PCOS mice (scale bar = 100 μm). ( b ) Quantification of CD163 + , F4/80 + , and F4/80 + CD163 + cell proportions in the ovaries and uteri of control and PCOS mice. * p < 0.05, ** p < 0.01, ns: p > 0.05.

Article Snippet: CD163 protein was acquired from MedChemExpress (Monmouth Junction, NJ, USA).

Techniques: Expressing, Immunofluorescence, Control

Increased M1 and M2 macrophages and elevated CD163 expression in M1 and M2 macrophages in the ovary and uterus of PCOS mice. ( a ) Representative immunofluorescence images of CD163, F4/80, iNOS, and Arg1 in the ovaries of control and PCOS mice (scale bar = 50 μm). ( b ) Representative immunofluorescence images of CD163, F4/80, iNOS, and Arg1 in the uterus of control and PCOS mice (scale bar = 50 μm). ( c ) Quantification of F4/80 + iNOS + CD163 + and F4/80 + Arg1 + CD163 + cell proportions in the ovaries. ( d ) Quantification of F4/80 + iNOS + CD163 + and F4/80 + Arg1 + CD163 + cell proportions in the uterus. * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Journal of Inflammation Research

Article Title: Increased CD163+ Macrophage Activation and High Expression of CD163 Promote Granulosa Cell Apoptosis in Polycystic Ovary Syndrome

doi: 10.2147/JIR.S532920

Figure Lengend Snippet: Increased M1 and M2 macrophages and elevated CD163 expression in M1 and M2 macrophages in the ovary and uterus of PCOS mice. ( a ) Representative immunofluorescence images of CD163, F4/80, iNOS, and Arg1 in the ovaries of control and PCOS mice (scale bar = 50 μm). ( b ) Representative immunofluorescence images of CD163, F4/80, iNOS, and Arg1 in the uterus of control and PCOS mice (scale bar = 50 μm). ( c ) Quantification of F4/80 + iNOS + CD163 + and F4/80 + Arg1 + CD163 + cell proportions in the ovaries. ( d ) Quantification of F4/80 + iNOS + CD163 + and F4/80 + Arg1 + CD163 + cell proportions in the uterus. * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: CD163 protein was acquired from MedChemExpress (Monmouth Junction, NJ, USA).

Techniques: Expressing, Immunofluorescence, Control

Increased apoptosis in CD163 + ovarian cells from PCOS mice. ( a ) Representative images of TUNEL and CD163 in the ovaries of control and PCOS mice via immunofluorescence analysis (scale bar = 50 μm). ( b ) Quantification of TUNEL + and CD163 + TUNEL + cell proportions in the ovaries. ** p < 0.01, *** p < 0.001.

Journal: Journal of Inflammation Research

Article Title: Increased CD163+ Macrophage Activation and High Expression of CD163 Promote Granulosa Cell Apoptosis in Polycystic Ovary Syndrome

doi: 10.2147/JIR.S532920

Figure Lengend Snippet: Increased apoptosis in CD163 + ovarian cells from PCOS mice. ( a ) Representative images of TUNEL and CD163 in the ovaries of control and PCOS mice via immunofluorescence analysis (scale bar = 50 μm). ( b ) Quantification of TUNEL + and CD163 + TUNEL + cell proportions in the ovaries. ** p < 0.01, *** p < 0.001.

Article Snippet: CD163 protein was acquired from MedChemExpress (Monmouth Junction, NJ, USA).

Techniques: TUNEL Assay, Control, Immunofluorescence

Effects of n-6 PUFA on liver macrophage phenotype in rats with NASH induced by a choline-deficient diet. (A) M1-type Kupffer cells (KCs) identified by double staining: red arrows show CD11c-positive cells, green arrows show CD68-positive cells, and yellow arrows highlight CD11c and CD68 double-positive M1-type KCs (Scale bar – 50 μM). (B) M2-type KCs identified similarly, with red arrows indicating CD163-positive cells, green arrows showing CD68-positive cells, and yellow arrows marking CD163 and CD68 double-positive M2-type KCs (Scale bar – 50 μM). For (A,B) (see ) for full-size photomicrographs. (C) M1/M2 phenotype ratio (unitless), calculated as the proportion of CD68 + CD11c + to CD68 + CD163 + cells. (D) Relative PPAR-γ2 mRNA expression (fold change normalized to GAPDH) in the liver, which is linked to macrophage polarization and inflammation. Data are expressed as mean ±SEM; n = 6/group.

Journal: Frontiers in Nutrition

Article Title: High intake of n-6 polyunsaturated fatty acid exacerbates non-alcoholic steatohepatitis by the involvement of multiple metabolic pathways

doi: 10.3389/fnut.2025.1562509

Figure Lengend Snippet: Effects of n-6 PUFA on liver macrophage phenotype in rats with NASH induced by a choline-deficient diet. (A) M1-type Kupffer cells (KCs) identified by double staining: red arrows show CD11c-positive cells, green arrows show CD68-positive cells, and yellow arrows highlight CD11c and CD68 double-positive M1-type KCs (Scale bar – 50 μM). (B) M2-type KCs identified similarly, with red arrows indicating CD163-positive cells, green arrows showing CD68-positive cells, and yellow arrows marking CD163 and CD68 double-positive M2-type KCs (Scale bar – 50 μM). For (A,B) (see ) for full-size photomicrographs. (C) M1/M2 phenotype ratio (unitless), calculated as the proportion of CD68 + CD11c + to CD68 + CD163 + cells. (D) Relative PPAR-γ2 mRNA expression (fold change normalized to GAPDH) in the liver, which is linked to macrophage polarization and inflammation. Data are expressed as mean ±SEM; n = 6/group.

Article Snippet: BCA protein quantitation kit (Boster Bio, Cat # AR0146), RIPA lysis buffer (Boster Bio, Cat # 0105), protease inhibitor cocktails (Boster, Bio Cat # AR1182), phosphatase inhibitor (Boster Bio, Cat # AR1183), color pre-dyed protein marker (Boster Bio, Cat # AR1113), Western-specific primary and secondary antibody diluent (Boster Bio, Cat # AR1017), wash buffer TBS-T (Boster Bio, Cat # AR0195-10), ECL chemiluminescent reagent (Boster Bio, Cat # AR1196), BSA TBS buffer system blocking solution (Boster Bio, Cat # AR0189), NF-κB antibody (Boster Bio, Cat # A01228-1), GAPDH antibody (Boster Bio, Cat # M00227), HRP-conjugated goat anti-rabbit IgG (Boster Bio, Cat # BA1054), CD163 antibody (Boster Bio, Cat # A00812-2), CD11c antibody (Boster Bio, Cat # A00357-3), CD68 antibody (Boster Bio, Cat # BA3638), fluorescent (DyLight 488) labeled goat anti-rabbit IgG (Boster Bio, Cat # BA1127), fluorescent (DyLight 594) labeled goat anti-rabbit IgG (Boster Bio, Cat # BA1142), rat TNF-α ELISA kit (Jiangsu Enzyme Immunoassay Co., Ltd., Cat # MM-0180R1), rat IL-1β ELISA kit (Boster Bio, Cat # EK0393), rat IL-4 ELISA kit (Jiangsu Enzyme Immunoassay Co., Ltd., Cat # MM-0191R1), rat IL-10 ELISA kit (Boster Bio, Cat # EK0418), 25 VD3 assay kit (Roche Diagnostics, Cat # 07028148190), TAOC assay kit (Nanjing Jiancheng, Cat # A015-3-1), MDA assay kit (Nanjing Jiancheng, Cat # A003-1-2), and free fatty acid kit (Kunchuang Biotechnology, Xian, China, Cat # SK125-2).

Techniques: Double Staining, Expressing

PTTG1 can induce the positive proportion of CD206 and CD163 in THP-1 cells. Transfection with overexpression vectors and siRNA sequences in SK-OV-3 and A2780 cells and incubation for 48 h. Changes in the proportion of positive cells of CD206 and CD163 by flow cytometry. (Compared between the two groups, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001)

Journal: Discover Oncology

Article Title: PTTG1 promotes M2 macrophage polarization via the cGMP-PKG signaling pathway and facilitates EMT progression in human epithelial ovarian cancer cells

doi: 10.1007/s12672-025-02512-4

Figure Lengend Snippet: PTTG1 can induce the positive proportion of CD206 and CD163 in THP-1 cells. Transfection with overexpression vectors and siRNA sequences in SK-OV-3 and A2780 cells and incubation for 48 h. Changes in the proportion of positive cells of CD206 and CD163 by flow cytometry. (Compared between the two groups, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001)

Article Snippet: CD163 , BOSTER , A00812-2 , 1:2000.

Techniques: Transfection, Over Expression, Incubation, Flow Cytometry

PTTG1 can enhance the protein and mRNA expression levels of CD206 and CD163 in THP-1 cells. Transfection with overexpression vectors and siRNA sequences in SK-OV-3 and A2780 cells and incubation for 48 h. The relative expression levels of proteins and mRNA of CD206 and CD163 by Western blotting and RT-qPCR. (Compared between the two groups, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001)

Journal: Discover Oncology

Article Title: PTTG1 promotes M2 macrophage polarization via the cGMP-PKG signaling pathway and facilitates EMT progression in human epithelial ovarian cancer cells

doi: 10.1007/s12672-025-02512-4

Figure Lengend Snippet: PTTG1 can enhance the protein and mRNA expression levels of CD206 and CD163 in THP-1 cells. Transfection with overexpression vectors and siRNA sequences in SK-OV-3 and A2780 cells and incubation for 48 h. The relative expression levels of proteins and mRNA of CD206 and CD163 by Western blotting and RT-qPCR. (Compared between the two groups, *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001)

Article Snippet: CD163 , BOSTER , A00812-2 , 1:2000.

Techniques: Expressing, Transfection, Over Expression, Incubation, Western Blot, Quantitative RT-PCR

Fig. 6. Immunohistochemical and FACS validations of M2pep-uIONP targeting M2 TAMs. Confocal microscopic images of tumor tissues collected from mice at 24 h after i.v. injection of probes show (A) Cy7-M2pep-uIONP were highly co-localizing with CD68- and CD163-double positive M2 TAM, revealing the targeting specificity. In comparison, the non-targeted control probe Cy7-scM2pep-uIONP and Cy7-Ferumoxytol not only exhibited much less tumoral accumulation, but also were not co-localized with M2 TAM. Scale bars: 37 µm. (B) Flow cytometric zebra plots and (C) the corresponding quantification of CD68- and CD163-double positive M2 TAM targeted by FITC-M2pep-uIONP, FITC-scM2pep-uIONP, and FITC-Ferumoxytol. The gating strategy involves sorting CD163+ M2 TAM population in live cells dissociated from mouse cerebrums by gating on CD68+ pan-macrophage populations, followed by further gating to assess the FITC-labeled nanoparticles.

Journal: Acta biomaterialia

Article Title: A subtype specific probe for targeted magnetic resonance imaging of M2 tumor-associated macrophages in brain tumors.

doi: 10.1016/j.actbio.2025.01.003

Figure Lengend Snippet: Fig. 6. Immunohistochemical and FACS validations of M2pep-uIONP targeting M2 TAMs. Confocal microscopic images of tumor tissues collected from mice at 24 h after i.v. injection of probes show (A) Cy7-M2pep-uIONP were highly co-localizing with CD68- and CD163-double positive M2 TAM, revealing the targeting specificity. In comparison, the non-targeted control probe Cy7-scM2pep-uIONP and Cy7-Ferumoxytol not only exhibited much less tumoral accumulation, but also were not co-localized with M2 TAM. Scale bars: 37 µm. (B) Flow cytometric zebra plots and (C) the corresponding quantification of CD68- and CD163-double positive M2 TAM targeted by FITC-M2pep-uIONP, FITC-scM2pep-uIONP, and FITC-Ferumoxytol. The gating strategy involves sorting CD163+ M2 TAM population in live cells dissociated from mouse cerebrums by gating on CD68+ pan-macrophage populations, followed by further gating to assess the FITC-labeled nanoparticles.

Article Snippet: Rabbit polyclonal anti-CD163 antibody was purchased from Boster Biological Technology (Pleasanton, CA, USA).

Techniques: Immunohistochemical staining, Injection, Comparison, Control, Labeling

Journal: International Journal of Molecular Sciences

Article Title: An Ingenane-Type Diterpene from Euphorbia kansui Promoted Cell Apoptosis and Macrophage Polarization via the Regulation of PKC Signaling Pathways

doi: 10.3390/ijms251810123

Figure Lengend Snippet: Compound A inhibited macrophages for polarized M2 phenotype in IL-4-stimulated RAW264.7 cells. ( a ) After treating with IL-4 (20 ng/mL) for 24 h, the expression and phosphorylation of PKC δ, ERK, and STAT6 were detected 0–60 min after compound A (10 μmol·L −1 ) treatment. Statistical significance was represented as follows: * p < 0.05, *** p < 0.001 versus 0 min group. ( b ) The expression and phosphorylation of STAT3 and STAT6 were detected 24 h after compound A treatment. Statistical significance was represented as follows: ### p < 0.001 versus C group; *** p < 0.001 versus IL-4 group. ( c ) The expression of TGF-β, CD163, CD206, ARG-1 was detected. ( d ) Representative images of immunofluorescence staining of CD206 (green) and DAPI (blue) of IL-4-induced RAW264.7 cells. Statistical significance was represented as follows: # p < 0.05, ## p < 0.01, ### p < 0.001 versus C group; ** p < 0.01, *** p < 0.001 versus IL-4 group.

Article Snippet: Bcl-2, Bax, ERK, and phospho-ERK were bought from CST (Cell Signaling Technology, Danvers, MA, USA), β-actin (Servicebio, Wuhan, China), ARG-1, CD163 (Beyotime, Shanghai, China), CD206 (Invitrogen-Thermo Fisher, Carlsbad, CA, USA).

Techniques: Expressing, Phospho-proteomics, Immunofluorescence, Staining

Review

Structured Review

Images

1) Product Images from "An Ingenane-Type Diterpene from Euphorbia kansui Promoted Cell Apoptosis and Macrophage Polarization via the Regulation of PKC Signaling Pathways"

Similar Products

Image Search Results