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apc anti mouse cd206 mmr antibody  (Elabscience Biotechnology)


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    Elabscience Biotechnology apc anti mouse cd206 mmr antibody
    Apc Anti Mouse Cd206 Mmr Antibody, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 80 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/apc+anti+mouse+cd206+mmr+antibody/APC+Anti-Mouse+CD206%2FMMR+Antibody/pm41961300-97-47-51
    Average 95 stars, based on 80 article reviews
    apc anti mouse cd206 mmr antibody - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    other:

    Article Title: Selenium-albumin corona rinse ameliorates diabetic periodontitis by inhibiting inflammation, anti-bacterial and improving osteogenesis via activating TrxR1/ROS/β-catenin anti-oxidation cascade.
    Article Snippet: Diabetes mellitus (DM) aggravates periodontitis due to disordered glucose metabolism, leading to accelerated bone destruction and increasing dental plaque reproduction to induce local inflammation.. The hyperglycemic state of DM leads to reactive oxygen species (ROS) overproduction that inhibits osteogenic differentiation in periodontal.. These make a great challenge for the treatment of diabetic periodontitis.

    Modification:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    Protease Inhibitor:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    SDS Page:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    Bicinchoninic Acid Protein Assay:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    Polyacrylamide Gel Electrophoresis:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    Marker:

    Article Title: Advancing the Identification of Bioactive Molecules and the Construction of a Synergistic Drug Delivery System in Combating Lung Injury.
    Article Snippet: .. Materials: Glabridin (GLA, ≥ 98%, Herbpurify, China), puerarin (PUE, ≥ 98%, Aladdin, China), Dulbecco’s Modified Eagle’s Medium (DMEM, Keygen BioTECN, China), Roswell Park Memorial Institute 1640 Medium (RPMI-1640, Keygen BioTECN, China), Fetal Bovine Serum (FBS, Sigma, Germany), H2DCFDA (Biosharp, China), confocal dishes (Biosharp, China), LPS (Solarbio, China), IL-4 (Novoprotein, China), PMA (Solarbio, China), DPPH (Macklin, China), Triton X-100 (Sangon Biotech, China), H2O2 (Nanjing Chemical Reagent, China), IL-1 beta Polyclonal antibody (Proteintech, China), HMGB1 Polyclonal antibody (Proteintech, China), GADD153 Polyclonal antibody (CHOP, Proteintech, China), calreticulin Polyclonal antibody (Proteintech, China), CoraLite647-conjugated Mouse Anti-Heavy Chain of Rabbit IgG (Proteintech, China), PE Anti-Mouse CD86 Antibody (Elabscience, China), APC Anti-Mouse CD206/MMR Antibody (Elabscience, China), Protease Inhibitor (Beyotime, China), SDS-PAGE Protein Sample Loading Buffer (5×) (Beyotime, China), Micro BCA Protein Assay Kit (Beyotime, China), MeilunGel Precast PAGE Gel (Meilun, China), Colour Mixed Protein Marker (Meilun, China). ..

    Staining:

    Article Title: A mitochondria-targeted nanomedicine for myocardial ischemia/reperfusion injury with synergistic antioxidant and anti-inflammatory properties
    Article Snippet: .. PE Anti-Mouse CD86 Antibody (Elabscience) or APC Anti-Mouse CD206/MMR Antibody (Elabscience) was used for staining, and the cells were detected by flow cytometry. .. C57BL/6 C mice (6–8 weeks, male) were obtained from Charles River Laboratories (Beijing, China) and were bred in a specific pathogen-free (SPF) environment.

    Article Title: A mitochondria-targeted nanomedicine for myocardial ischemia/reperfusion injury with synergistic antioxidant and anti-inflammatory properties.
    Article Snippet: .. PE Anti-Mouse CD86 Antibody (Elabscience) or APC Anti-Mouse CD206/ MMR Antibody (Elabscience) was used for staining, and the cells were detected by flow cytometry. .. Myocardial infarction injury model in mouse C57BL/6 C mice (6–8 weeks, male) were obtained from Charles River Laboratories (Beijing, China) and were bred in a specific pathogen-free (SPF) environment.

    Article Title: Suppression of Nr1d1/Bnip3-dependent mitophagy by notch signaling aggravates inflammatory response in RSV-infected mice lungs.
    Article Snippet: 1 Department of Pediatrics, Women and Children’s Hospital, Zhongnan Hospital of Wuhan University, 169# Donghu Road, Wuhan 430062, Hubei, China 2 Jingmen Central Hospital, Central Hospital affiliated to Jingchu University of Technology, Jingmen, China 3 Children’s Digital Health and Data Center, Wuhan University, Wuhan 430062, Hubei, China Abstract Background Alveolar macrophages (AMs) are crucial for defending against respiratory syncytial virus (RSV) and regulating lung inflammation.. Notch signaling is essential for macrophage polarization and its functional diversity.However, the role of macrophages Notch1 in RSV-induced lung injury and its underlying mechanisms remain incompletely understood.. Methods This study used macrophage-specific Notch1 knockout (MKO) mice to investigate the lung lesions and inflammation in RSV-infected mice.

    Flow Cytometry:

    Article Title: A mitochondria-targeted nanomedicine for myocardial ischemia/reperfusion injury with synergistic antioxidant and anti-inflammatory properties
    Article Snippet: .. PE Anti-Mouse CD86 Antibody (Elabscience) or APC Anti-Mouse CD206/MMR Antibody (Elabscience) was used for staining, and the cells were detected by flow cytometry. .. C57BL/6 C mice (6–8 weeks, male) were obtained from Charles River Laboratories (Beijing, China) and were bred in a specific pathogen-free (SPF) environment.

    Article Title: A mitochondria-targeted nanomedicine for myocardial ischemia/reperfusion injury with synergistic antioxidant and anti-inflammatory properties.
    Article Snippet: .. PE Anti-Mouse CD86 Antibody (Elabscience) or APC Anti-Mouse CD206/ MMR Antibody (Elabscience) was used for staining, and the cells were detected by flow cytometry. .. Myocardial infarction injury model in mouse C57BL/6 C mice (6–8 weeks, male) were obtained from Charles River Laboratories (Beijing, China) and were bred in a specific pathogen-free (SPF) environment.

    Article Title: PRSS23 functions downstream of ZEB1 to promote esophageal squamous cell carcinoma progression by driving M2 polarization of tumor associated macrophages.
    Article Snippet: factors were considered to be associated with the development of EC, such as smoking, alcohol abuse, obesity [5].. EC incudes two main histological subtypes: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) [4].. ESCC most frequently originates in the middle to upper esophagus and accounts for 90% of EC cases in Asia [3, 6, 7].

    Incubation:

    Article Title: PRSS23 functions downstream of ZEB1 to promote esophageal squamous cell carcinoma progression by driving M2 polarization of tumor associated macrophages.
    Article Snippet: factors were considered to be associated with the development of EC, such as smoking, alcohol abuse, obesity [5].. EC incudes two main histological subtypes: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC) [4].. ESCC most frequently originates in the middle to upper esophagus and accounts for 90% of EC cases in Asia [3, 6, 7].



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    Elabscience Biotechnology cd206
    MM cell-derived ETV1 fosters M2 polarization of TAMs. ( A ) THP-1 cells were incubated with 350 nM PMA for 24 h to induce M0 macrophage differentiation. The morphology of M0 macrophages was photographed with a microscope. ( B ) The proportion of CD68 + cells in M0 macrophages were detected by flow cytometry. ( C ) M2 polarization of TAMs was measured by Transwell co-culture system. M0 macrophages were seeded into the lower chamber, and MM cells were seeded into the upper chamber. ( D ) The levels of CCL2 in MM cells was tested by qPCR and ELISA. ( E ) After 48 h of co-culture, the expression of CD163, Arg-1 and <t>CD206</t> in M0 macrophages was determined by qPCR. ( F ) The proportion of CD206 + cells and MFI in M0 macrophages were examined by flow cytometry. Data are mean ± SD. #, p < 0.05; ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001
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    Image Search Results


    MM cell-derived ETV1 fosters M2 polarization of TAMs. ( A ) THP-1 cells were incubated with 350 nM PMA for 24 h to induce M0 macrophage differentiation. The morphology of M0 macrophages was photographed with a microscope. ( B ) The proportion of CD68 + cells in M0 macrophages were detected by flow cytometry. ( C ) M2 polarization of TAMs was measured by Transwell co-culture system. M0 macrophages were seeded into the lower chamber, and MM cells were seeded into the upper chamber. ( D ) The levels of CCL2 in MM cells was tested by qPCR and ELISA. ( E ) After 48 h of co-culture, the expression of CD163, Arg-1 and CD206 in M0 macrophages was determined by qPCR. ( F ) The proportion of CD206 + cells and MFI in M0 macrophages were examined by flow cytometry. Data are mean ± SD. #, p < 0.05; ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Journal: Journal of Translational Medicine

    Article Title: m6A methylation-modified ETV1 drives multiple myeloma progression and M2 polarization of tumor-associated macrophage through transcriptional activation of RBMS1

    doi: 10.1186/s12967-026-07799-7

    Figure Lengend Snippet: MM cell-derived ETV1 fosters M2 polarization of TAMs. ( A ) THP-1 cells were incubated with 350 nM PMA for 24 h to induce M0 macrophage differentiation. The morphology of M0 macrophages was photographed with a microscope. ( B ) The proportion of CD68 + cells in M0 macrophages were detected by flow cytometry. ( C ) M2 polarization of TAMs was measured by Transwell co-culture system. M0 macrophages were seeded into the lower chamber, and MM cells were seeded into the upper chamber. ( D ) The levels of CCL2 in MM cells was tested by qPCR and ELISA. ( E ) After 48 h of co-culture, the expression of CD163, Arg-1 and CD206 in M0 macrophages was determined by qPCR. ( F ) The proportion of CD206 + cells and MFI in M0 macrophages were examined by flow cytometry. Data are mean ± SD. #, p < 0.05; ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Article Snippet: For detection of CD11b+F4/80 + CD206+, cells were collected by centrifugation, and 5 μl mouse CD11b antibody (E-AB-F1081D, Elabscience, Wuhan, China), 5 μl mouse F4/80 antibody (E-AB-F0995J, Elabscience), and 5 μl mouse CD206 antibody (E-AB-F1135E, Elabscience) were added and incubated in the dark for 30 min.

    Techniques: Derivative Assay, Incubation, Microscopy, Flow Cytometry, Co-Culture Assay, Enzyme-linked Immunosorbent Assay, Expressing

    ETV1 facilitates tumor growth and M2 polarization of macrophages in vivo. ( A ) The development of tumors was determined by the in vivo fluorescence imaging system. ( B ) H&E staining was used to detect tumor formation in bone tissues of mice. (Scale bar = 100 μm). ( C ) Immunohistochemical staining was used to examine the expression of human ETV1 in bone marrow tissues. (Scale bar = 50 μm). ( D ) Flow cytometry was used to test the proportion of mouse-derived M2 phenotypic macrophages (F4/80 + CD206+/F4/80+) in M0 macrophages (F4/80+) in bone marrow tissues. ( E ) The expression of human CCL2 in bone marrow tissues was detected by western blot. Data are mean ± SD. ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Journal: Journal of Translational Medicine

    Article Title: m6A methylation-modified ETV1 drives multiple myeloma progression and M2 polarization of tumor-associated macrophage through transcriptional activation of RBMS1

    doi: 10.1186/s12967-026-07799-7

    Figure Lengend Snippet: ETV1 facilitates tumor growth and M2 polarization of macrophages in vivo. ( A ) The development of tumors was determined by the in vivo fluorescence imaging system. ( B ) H&E staining was used to detect tumor formation in bone tissues of mice. (Scale bar = 100 μm). ( C ) Immunohistochemical staining was used to examine the expression of human ETV1 in bone marrow tissues. (Scale bar = 50 μm). ( D ) Flow cytometry was used to test the proportion of mouse-derived M2 phenotypic macrophages (F4/80 + CD206+/F4/80+) in M0 macrophages (F4/80+) in bone marrow tissues. ( E ) The expression of human CCL2 in bone marrow tissues was detected by western blot. Data are mean ± SD. ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Article Snippet: For detection of CD11b+F4/80 + CD206+, cells were collected by centrifugation, and 5 μl mouse CD11b antibody (E-AB-F1081D, Elabscience, Wuhan, China), 5 μl mouse F4/80 antibody (E-AB-F0995J, Elabscience), and 5 μl mouse CD206 antibody (E-AB-F1135E, Elabscience) were added and incubated in the dark for 30 min.

    Techniques: In Vivo, Fluorescence, Imaging, Staining, Immunohistochemical staining, Expressing, Flow Cytometry, Derivative Assay, Western Blot

    RBMS1 knockdown counteracts the effect of ETV1 overexpression on MM cell proliferation and M2 polarization of TAMs. ( A ) siRNAs targeting RBMS1 were transfected into RPMI8226 cells. After 48 h, the knockdown efficiency of RBMS1 in cells was verified by qPCR. ( B ) Cell viability was measured by CCK-8 assay. ( C ) Cell cycle distribution was detected by flow cytometry. ( D ) The expression of cyclinD1 in cells was detected by western blot. ( E ) The levels of CCL2 in the cell supernatant were determined by ELISA. ( F ) M2 polarization of TAMs was tested by Transwell co-culture system. M0 macrophages were seeded into the lower chamber, and MM cells were seeded into the upper chamber. After 48 h of co-culture, the expression of CD163 and CD206 in M0 macrophages were determined by qPCR. ( G ) The proportion of CD206 + cells and MFI in M0 macrophages were examined by flow cytometry. Data are mean ± SD. #, p < 0.05; ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Journal: Journal of Translational Medicine

    Article Title: m6A methylation-modified ETV1 drives multiple myeloma progression and M2 polarization of tumor-associated macrophage through transcriptional activation of RBMS1

    doi: 10.1186/s12967-026-07799-7

    Figure Lengend Snippet: RBMS1 knockdown counteracts the effect of ETV1 overexpression on MM cell proliferation and M2 polarization of TAMs. ( A ) siRNAs targeting RBMS1 were transfected into RPMI8226 cells. After 48 h, the knockdown efficiency of RBMS1 in cells was verified by qPCR. ( B ) Cell viability was measured by CCK-8 assay. ( C ) Cell cycle distribution was detected by flow cytometry. ( D ) The expression of cyclinD1 in cells was detected by western blot. ( E ) The levels of CCL2 in the cell supernatant were determined by ELISA. ( F ) M2 polarization of TAMs was tested by Transwell co-culture system. M0 macrophages were seeded into the lower chamber, and MM cells were seeded into the upper chamber. After 48 h of co-culture, the expression of CD163 and CD206 in M0 macrophages were determined by qPCR. ( G ) The proportion of CD206 + cells and MFI in M0 macrophages were examined by flow cytometry. Data are mean ± SD. #, p < 0.05; ##, p < 0.01; ###, p < 0.001; ####, p < 0.0001

    Article Snippet: For detection of CD11b+F4/80 + CD206+, cells were collected by centrifugation, and 5 μl mouse CD11b antibody (E-AB-F1081D, Elabscience, Wuhan, China), 5 μl mouse F4/80 antibody (E-AB-F0995J, Elabscience), and 5 μl mouse CD206 antibody (E-AB-F1135E, Elabscience) were added and incubated in the dark for 30 min.

    Techniques: Knockdown, Over Expression, Transfection, CCK-8 Assay, Flow Cytometry, Expressing, Western Blot, Enzyme-linked Immunosorbent Assay, Co-Culture Assay