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mouse monoclonal antibody against stat6  (Proteintech)


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    Structured Review

    Proteintech mouse monoclonal antibody against stat6
    KLF4 is associated with sleep deprivation-induced ADRB2 modulation of macrophage prompting on proliferation, migration, and invasion of LLC-LUC cells (A) Differentially expressed Top20 genes in metastatic lung tissues of NC group and sleep deprivation group. (B) The expression of top 5 upregulated genes in tumor tissues was analyzed by qRT-PCR. (C) KLF4 expression was detected by ADRB2-specific agonist ISO and ADRB2 antagonist ICI118,551 in macrophages treated with IL-4 in vitro . (D) The effect of ADRB2 agonist on CD206 expression in IL-4-induced KLF4-knockdown macrophages. (E) EdU assays showed the proliferation of tumor cells in the coculture system with 30% CM. CM derived from IL-4 and IL-4 + ISO induced supernatant of macrophages with KLF4 low and high expression. (F) The migration ability of tumor cells was determined by wound healing assays in the indicated coculture medium. (G) Transwell assays demonstrated invasion of tumor cells in the indicated coculture system. (H) Representative IHC images of p-JAK1 and <t>p-STAT6</t> in xenograft tumors. (I) The phosphorylation of JAK1 and STAT6 expression in RAW264.7 treated with ADRB2 agonist or antagonist via Western blotting. (J) Immunoblotting of KLF4 in RAW264.7 treated with different conditions. Data represented as mean ± SD. Statistical analysis was performed using Student’s t test or Mann-Whitney U test. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.
    Mouse Monoclonal Antibody Against Stat6, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 72 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+monoclonal+antibody+against+stat6/STAT6+Antibody/pmc12018092-458-34-39
    Average 95 stars, based on 72 article reviews
    mouse monoclonal antibody against stat6 - by Bioz Stars, 2026-10
    95/100 stars

    Images

    1) Product Images from "Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis"

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis

    Journal: iScience

    doi: 10.1016/j.isci.2025.112321

    KLF4 is associated with sleep deprivation-induced ADRB2 modulation of macrophage prompting on proliferation, migration, and invasion of LLC-LUC cells (A) Differentially expressed Top20 genes in metastatic lung tissues of NC group and sleep deprivation group. (B) The expression of top 5 upregulated genes in tumor tissues was analyzed by qRT-PCR. (C) KLF4 expression was detected by ADRB2-specific agonist ISO and ADRB2 antagonist ICI118,551 in macrophages treated with IL-4 in vitro . (D) The effect of ADRB2 agonist on CD206 expression in IL-4-induced KLF4-knockdown macrophages. (E) EdU assays showed the proliferation of tumor cells in the coculture system with 30% CM. CM derived from IL-4 and IL-4 + ISO induced supernatant of macrophages with KLF4 low and high expression. (F) The migration ability of tumor cells was determined by wound healing assays in the indicated coculture medium. (G) Transwell assays demonstrated invasion of tumor cells in the indicated coculture system. (H) Representative IHC images of p-JAK1 and p-STAT6 in xenograft tumors. (I) The phosphorylation of JAK1 and STAT6 expression in RAW264.7 treated with ADRB2 agonist or antagonist via Western blotting. (J) Immunoblotting of KLF4 in RAW264.7 treated with different conditions. Data represented as mean ± SD. Statistical analysis was performed using Student’s t test or Mann-Whitney U test. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.
    Figure Legend Snippet: KLF4 is associated with sleep deprivation-induced ADRB2 modulation of macrophage prompting on proliferation, migration, and invasion of LLC-LUC cells (A) Differentially expressed Top20 genes in metastatic lung tissues of NC group and sleep deprivation group. (B) The expression of top 5 upregulated genes in tumor tissues was analyzed by qRT-PCR. (C) KLF4 expression was detected by ADRB2-specific agonist ISO and ADRB2 antagonist ICI118,551 in macrophages treated with IL-4 in vitro . (D) The effect of ADRB2 agonist on CD206 expression in IL-4-induced KLF4-knockdown macrophages. (E) EdU assays showed the proliferation of tumor cells in the coculture system with 30% CM. CM derived from IL-4 and IL-4 + ISO induced supernatant of macrophages with KLF4 low and high expression. (F) The migration ability of tumor cells was determined by wound healing assays in the indicated coculture medium. (G) Transwell assays demonstrated invasion of tumor cells in the indicated coculture system. (H) Representative IHC images of p-JAK1 and p-STAT6 in xenograft tumors. (I) The phosphorylation of JAK1 and STAT6 expression in RAW264.7 treated with ADRB2 agonist or antagonist via Western blotting. (J) Immunoblotting of KLF4 in RAW264.7 treated with different conditions. Data represented as mean ± SD. Statistical analysis was performed using Student’s t test or Mann-Whitney U test. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.

    Techniques Used: Migration, Expressing, Quantitative RT-PCR, In Vitro, Knockdown, Derivative Assay, Phospho-proteomics, Western Blot, MANN-WHITNEY

    NE level is elevated in NSCLC patients with sleep deprivation and is associated with a poor prognosis (A) The concentration of NE in serum of the NSCLC patients, determined by ELISA assay. (B) Representative IHC images and quantitative analysis of ADRB2 in the NSCLC patients. (C) Representative IHC images and quantitative analysis of KLF4 in the NSCLC patients. (D) Investigation into the association between ADRB2 expression and immune cell infiltration in patients diagnosed with LUAD. (E) Analysis of the correlation between KLF4 and immune cell infiltration in LUAD patients. (F–H) Correlation analysis between ADRB2, KLF4, JAK1, and STAT6 expression. (I and J) Correlation analysis between KLF4, JAK1, and STAT6 expression. (K and L) Correlation analysis between JAK1, STAT6, and pro-tumoral macrophages. Data represented as mean ± SD. Statistical analysis was evaluated using Student’s t test. ∗∗ p < 0.01 and ∗∗∗ p < 0.001.
    Figure Legend Snippet: NE level is elevated in NSCLC patients with sleep deprivation and is associated with a poor prognosis (A) The concentration of NE in serum of the NSCLC patients, determined by ELISA assay. (B) Representative IHC images and quantitative analysis of ADRB2 in the NSCLC patients. (C) Representative IHC images and quantitative analysis of KLF4 in the NSCLC patients. (D) Investigation into the association between ADRB2 expression and immune cell infiltration in patients diagnosed with LUAD. (E) Analysis of the correlation between KLF4 and immune cell infiltration in LUAD patients. (F–H) Correlation analysis between ADRB2, KLF4, JAK1, and STAT6 expression. (I and J) Correlation analysis between KLF4, JAK1, and STAT6 expression. (K and L) Correlation analysis between JAK1, STAT6, and pro-tumoral macrophages. Data represented as mean ± SD. Statistical analysis was evaluated using Student’s t test. ∗∗ p < 0.01 and ∗∗∗ p < 0.001.

    Techniques Used: Concentration Assay, Enzyme-linked Immunosorbent Assay, Expressing


    Figure Legend Snippet:

    Techniques Used: Recombinant, Transfection, Enzyme-linked Immunosorbent Assay, Phagocytosis Assay, Sequencing, Software

    Related Articles

    Blocking Assay:

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis
    Article Snippet: .. After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies. ..

    Incubation:

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis
    Article Snippet: .. After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies. ..

    Saline:

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis
    Article Snippet: .. After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies. ..



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    Image Search Results


    KLF4 is associated with sleep deprivation-induced ADRB2 modulation of macrophage prompting on proliferation, migration, and invasion of LLC-LUC cells (A) Differentially expressed Top20 genes in metastatic lung tissues of NC group and sleep deprivation group. (B) The expression of top 5 upregulated genes in tumor tissues was analyzed by qRT-PCR. (C) KLF4 expression was detected by ADRB2-specific agonist ISO and ADRB2 antagonist ICI118,551 in macrophages treated with IL-4 in vitro . (D) The effect of ADRB2 agonist on CD206 expression in IL-4-induced KLF4-knockdown macrophages. (E) EdU assays showed the proliferation of tumor cells in the coculture system with 30% CM. CM derived from IL-4 and IL-4 + ISO induced supernatant of macrophages with KLF4 low and high expression. (F) The migration ability of tumor cells was determined by wound healing assays in the indicated coculture medium. (G) Transwell assays demonstrated invasion of tumor cells in the indicated coculture system. (H) Representative IHC images of p-JAK1 and p-STAT6 in xenograft tumors. (I) The phosphorylation of JAK1 and STAT6 expression in RAW264.7 treated with ADRB2 agonist or antagonist via Western blotting. (J) Immunoblotting of KLF4 in RAW264.7 treated with different conditions. Data represented as mean ± SD. Statistical analysis was performed using Student’s t test or Mann-Whitney U test. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.

    Journal: iScience

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis

    doi: 10.1016/j.isci.2025.112321

    Figure Lengend Snippet: KLF4 is associated with sleep deprivation-induced ADRB2 modulation of macrophage prompting on proliferation, migration, and invasion of LLC-LUC cells (A) Differentially expressed Top20 genes in metastatic lung tissues of NC group and sleep deprivation group. (B) The expression of top 5 upregulated genes in tumor tissues was analyzed by qRT-PCR. (C) KLF4 expression was detected by ADRB2-specific agonist ISO and ADRB2 antagonist ICI118,551 in macrophages treated with IL-4 in vitro . (D) The effect of ADRB2 agonist on CD206 expression in IL-4-induced KLF4-knockdown macrophages. (E) EdU assays showed the proliferation of tumor cells in the coculture system with 30% CM. CM derived from IL-4 and IL-4 + ISO induced supernatant of macrophages with KLF4 low and high expression. (F) The migration ability of tumor cells was determined by wound healing assays in the indicated coculture medium. (G) Transwell assays demonstrated invasion of tumor cells in the indicated coculture system. (H) Representative IHC images of p-JAK1 and p-STAT6 in xenograft tumors. (I) The phosphorylation of JAK1 and STAT6 expression in RAW264.7 treated with ADRB2 agonist or antagonist via Western blotting. (J) Immunoblotting of KLF4 in RAW264.7 treated with different conditions. Data represented as mean ± SD. Statistical analysis was performed using Student’s t test or Mann-Whitney U test. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.

    Article Snippet: After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies.

    Techniques: Migration, Expressing, Quantitative RT-PCR, In Vitro, Knockdown, Derivative Assay, Phospho-proteomics, Western Blot, MANN-WHITNEY

    NE level is elevated in NSCLC patients with sleep deprivation and is associated with a poor prognosis (A) The concentration of NE in serum of the NSCLC patients, determined by ELISA assay. (B) Representative IHC images and quantitative analysis of ADRB2 in the NSCLC patients. (C) Representative IHC images and quantitative analysis of KLF4 in the NSCLC patients. (D) Investigation into the association between ADRB2 expression and immune cell infiltration in patients diagnosed with LUAD. (E) Analysis of the correlation between KLF4 and immune cell infiltration in LUAD patients. (F–H) Correlation analysis between ADRB2, KLF4, JAK1, and STAT6 expression. (I and J) Correlation analysis between KLF4, JAK1, and STAT6 expression. (K and L) Correlation analysis between JAK1, STAT6, and pro-tumoral macrophages. Data represented as mean ± SD. Statistical analysis was evaluated using Student’s t test. ∗∗ p < 0.01 and ∗∗∗ p < 0.001.

    Journal: iScience

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis

    doi: 10.1016/j.isci.2025.112321

    Figure Lengend Snippet: NE level is elevated in NSCLC patients with sleep deprivation and is associated with a poor prognosis (A) The concentration of NE in serum of the NSCLC patients, determined by ELISA assay. (B) Representative IHC images and quantitative analysis of ADRB2 in the NSCLC patients. (C) Representative IHC images and quantitative analysis of KLF4 in the NSCLC patients. (D) Investigation into the association between ADRB2 expression and immune cell infiltration in patients diagnosed with LUAD. (E) Analysis of the correlation between KLF4 and immune cell infiltration in LUAD patients. (F–H) Correlation analysis between ADRB2, KLF4, JAK1, and STAT6 expression. (I and J) Correlation analysis between KLF4, JAK1, and STAT6 expression. (K and L) Correlation analysis between JAK1, STAT6, and pro-tumoral macrophages. Data represented as mean ± SD. Statistical analysis was evaluated using Student’s t test. ∗∗ p < 0.01 and ∗∗∗ p < 0.001.

    Article Snippet: After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies.

    Techniques: Concentration Assay, Enzyme-linked Immunosorbent Assay, Expressing

    Journal: iScience

    Article Title: Sleep deprivation-induced sympathetic activation promotes pro-tumoral macrophage phenotype via the ADRB2/KLF4 pathway to facilitate NSCLC metastasis

    doi: 10.1016/j.isci.2025.112321

    Figure Lengend Snippet:

    Article Snippet: After blocking the membranes with 5% BSA for 1 h, they were incubated with primary antibodies against KLF4 (Proteintech, Wuhan, China), mouse monoclonal antibody against JAK1 (Proteintech), rabbit polyclonal antibody against p-JAK1 (ImmunoWay, USA), mouse monoclonal antibody against STAT6 (Proteintech) and rabbit polyclonal antibody against p-STAT6 (ImmunoWay) for 2 h, followed by three washes with Tris-buffered saline containing Tween-20 (TBST), and then incubated with appropriate secondary antibodies.

    Techniques: Recombinant, Transfection, Enzyme-linked Immunosorbent Assay, Phagocytosis Assay, Sequencing, Software

    AT-RvD1 downregulates the NF- κ B (a) and STAT6 (b) pathways in bronchial epithelial cells stimulated with IL-4. BEAS-2B cells were stimulated with IL-4 (25 ng/mL) for 15 min in the presence or absence of AT-RvD1 (100 nM). The results are expressed as the arithmetic mean plus SEM from three independent experiments ( n = 4). ∗ P < 0.05 versus control group; # P < 0.05 versus IL-4-treated group.

    Journal: BioMed Research International

    Article Title: AT-RvD1 Modulates CCL-2 and CXCL-8 Production and NF- κ B, STAT-6, SOCS1, and SOCS3 Expression on Bronchial Epithelial Cells Stimulated with IL-4

    doi: 10.1155/2015/178369

    Figure Lengend Snippet: AT-RvD1 downregulates the NF- κ B (a) and STAT6 (b) pathways in bronchial epithelial cells stimulated with IL-4. BEAS-2B cells were stimulated with IL-4 (25 ng/mL) for 15 min in the presence or absence of AT-RvD1 (100 nM). The results are expressed as the arithmetic mean plus SEM from three independent experiments ( n = 4). ∗ P < 0.05 versus control group; # P < 0.05 versus IL-4-treated group.

    Article Snippet: After centrifugation, the cells were permeabilized in ice-cold methanol for 30 min and then stained with mouse monoclonal antibodies against anti-NF- κ B (BD Biosciences Pharmingen, Phosflow, USA), anti-STAT6 (BD Biosciences Pharmingen, Phosflow, USA), or their corresponding mouse IgG2b isotype (BD Biosciences Pharmingen, Phosflow, USA) for 60 min followed by an FITC- or PE-conjugated goat anti-mouse IgG2b secondary antibody for another 45 min at 10°C in the dark.

    Techniques:

    Immunocytochemical findings. STAT6 is diffusely expressed (magnification, ×400). STAT6, signal transducer and activator of transcription 6.

    Journal: Molecular and Clinical Oncology

    Article Title: Cytological characteristics of meningeal solitary fibrous tumor metastatic to the lung: A case report with immunocytochemical analysis

    doi: 10.3892/mco.2018.1625

    Figure Lengend Snippet: Immunocytochemical findings. STAT6 is diffusely expressed (magnification, ×400). STAT6, signal transducer and activator of transcription 6.

    Article Snippet: The primary antibodies used in this report were mouse monoclonal antibody against B-cell lymphoma 2 (Bcl-2; 124), mouse monoclonal antibody against CD34 (QBEnd10), mouse monoclonal antibody against Ki-67 (MIB1) (all from DAKO) and mouse monoclonal antibody against STAT6 (D-1, Santa Cruz Biotechnology, Dallas, TX, USA).

    Techniques:

    Immunohistochemical characteristics of the lung nodule. (A) STAT6, (B) Bcl-2 and (C) CD34 are diffusely expressed (magnification, ×400). STAT6, signal transducer and activator of transcription 6; Bcl-2, B-cell lymphoma 2.

    Journal: Molecular and Clinical Oncology

    Article Title: Cytological characteristics of meningeal solitary fibrous tumor metastatic to the lung: A case report with immunocytochemical analysis

    doi: 10.3892/mco.2018.1625

    Figure Lengend Snippet: Immunohistochemical characteristics of the lung nodule. (A) STAT6, (B) Bcl-2 and (C) CD34 are diffusely expressed (magnification, ×400). STAT6, signal transducer and activator of transcription 6; Bcl-2, B-cell lymphoma 2.

    Article Snippet: The primary antibodies used in this report were mouse monoclonal antibody against B-cell lymphoma 2 (Bcl-2; 124), mouse monoclonal antibody against CD34 (QBEnd10), mouse monoclonal antibody against Ki-67 (MIB1) (all from DAKO) and mouse monoclonal antibody against STAT6 (D-1, Santa Cruz Biotechnology, Dallas, TX, USA).

    Techniques: Immunohistochemical staining