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phospho stat3  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc phospho stat3
    KPF ameliorates placental pathological changes and oxidative stress in GDM rats. (A) HE staining was performed to evaluate pathological alterations in placental tissues. Magnification: 100×; scale bar: 200 μm. (B) PAS staining was performed to assess glycogen distribution and deposition in placental tissues. Magnification: 100×; scale bar: 200 μm. (C, D) DHE staining was performed to evaluate ROS accumulation in placental tissues. Magnification: 200×; scale bar: 20 μm. (E–I) Western blot analysis was performed to determine the protein expression levels of AIM2, <t>p-STAT3,</t> GPX4, and SLC7A11 in placental tissues. N = 3, * P < 0.05, ** P < 0.01, *** P < 0.001.
    Phospho Stat3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 6135 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+phospho+stat3+antibody/Phospho-Stat3+(Tyr705)+XP+Rabbit+mAb/pmc13640141-140-39-43
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    Images

    1) Product Images from "Kaempferol ameliorates gestational diabetes mellitus by regulating STAT3-associated AIM2 inflammasome activation and ferroptotic injury in trophoblasts"

    Article Title: Kaempferol ameliorates gestational diabetes mellitus by regulating STAT3-associated AIM2 inflammasome activation and ferroptotic injury in trophoblasts

    Journal: Frontiers in Physiology

    doi: 10.3389/fphys.2026.1857741

    KPF ameliorates placental pathological changes and oxidative stress in GDM rats. (A) HE staining was performed to evaluate pathological alterations in placental tissues. Magnification: 100×; scale bar: 200 μm. (B) PAS staining was performed to assess glycogen distribution and deposition in placental tissues. Magnification: 100×; scale bar: 200 μm. (C, D) DHE staining was performed to evaluate ROS accumulation in placental tissues. Magnification: 200×; scale bar: 20 μm. (E–I) Western blot analysis was performed to determine the protein expression levels of AIM2, p-STAT3, GPX4, and SLC7A11 in placental tissues. N = 3, * P < 0.05, ** P < 0.01, *** P < 0.001.
    Figure Legend Snippet: KPF ameliorates placental pathological changes and oxidative stress in GDM rats. (A) HE staining was performed to evaluate pathological alterations in placental tissues. Magnification: 100×; scale bar: 200 μm. (B) PAS staining was performed to assess glycogen distribution and deposition in placental tissues. Magnification: 100×; scale bar: 200 μm. (C, D) DHE staining was performed to evaluate ROS accumulation in placental tissues. Magnification: 200×; scale bar: 20 μm. (E–I) Western blot analysis was performed to determine the protein expression levels of AIM2, p-STAT3, GPX4, and SLC7A11 in placental tissues. N = 3, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Techniques Used: H&E Stain, Staining, Western Blot, Analysis, Expressing

    KPF modulates trophoblast inflammatory responses and ferroptosis-related alterations through STAT3-associated signaling regulation. (A) Molecular docking analysis showing the potential interaction between KPF and STAT3 protein. (B, C) RT-qPCR analysis of STAT3 mRNA expression and transfection efficiency in HTR-8/SVneo cells. (D) CCK-8 assay was used to evaluate cell viability. (E, F) ELISA quantification of inflammatory cytokines IL-18 and TNF-α in cell supernatants. (G–L) Western blot analysis of AIM2, IL-1β, pro-IL-1β, GPX4, SLC7A11, cleaved caspase-1, and pro-caspase-1 protein expression in cells subjected to various treatments. (M–P) Western blot analysis of STAT3-associated changes in STAT3, GPX4, and SLC7A11 protein expression in cells subjected to various treatments. N = 3, not significant, * P < 0.05, ** P < 0.01, *** P < 0.001.
    Figure Legend Snippet: KPF modulates trophoblast inflammatory responses and ferroptosis-related alterations through STAT3-associated signaling regulation. (A) Molecular docking analysis showing the potential interaction between KPF and STAT3 protein. (B, C) RT-qPCR analysis of STAT3 mRNA expression and transfection efficiency in HTR-8/SVneo cells. (D) CCK-8 assay was used to evaluate cell viability. (E, F) ELISA quantification of inflammatory cytokines IL-18 and TNF-α in cell supernatants. (G–L) Western blot analysis of AIM2, IL-1β, pro-IL-1β, GPX4, SLC7A11, cleaved caspase-1, and pro-caspase-1 protein expression in cells subjected to various treatments. (M–P) Western blot analysis of STAT3-associated changes in STAT3, GPX4, and SLC7A11 protein expression in cells subjected to various treatments. N = 3, not significant, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Techniques Used: Docking Assay, Analysis, Quantitative RT-PCR, Expressing, Transfection, CCK-8 Assay, Enzyme-linked Immunosorbent Assay, Western Blot

    STAT3-associated changes in STAT1/IRF1 signaling and AIM2 expression in HG-stimulated trophoblast cells. (A, B) RT-qPCR was performed to assess STAT3 knockdown efficiency and AIM2 mRNA expression changes in HTR-8/SVneo cells subjected to different treatments. (C–F) Western blot analysis was performed to evaluate the expression levels of p-STAT1, STAT1, IRF1, and AIM2 proteins under different experimental conditions. N = 3, not significant, ** P <0.01, *** P <0.001.
    Figure Legend Snippet: STAT3-associated changes in STAT1/IRF1 signaling and AIM2 expression in HG-stimulated trophoblast cells. (A, B) RT-qPCR was performed to assess STAT3 knockdown efficiency and AIM2 mRNA expression changes in HTR-8/SVneo cells subjected to different treatments. (C–F) Western blot analysis was performed to evaluate the expression levels of p-STAT1, STAT1, IRF1, and AIM2 proteins under different experimental conditions. N = 3, not significant, ** P <0.01, *** P <0.001.

    Techniques Used: Expressing, Quantitative RT-PCR, Knockdown, Western Blot, Analysis

    Related Articles

    other:

    Article Title: Co-targeting CDK4/6 enhances anti-cancer activity and alleviates immune-related adverse events of anti-PD-1 antibody for breast cancer
    Article Snippet: Anti-Phospho-Stat3 antibody , Cell Signaling , #9145; RRID: AB_2491009.

    SDS Page:

    Article Title: Peptides inhibiting gamma-c-cytokine activity and methods of use
    Article Snippet: .. The extracted cytoplasmic proteins were resolved using a standard SDS-PAGE (Sodium Dodecyl-Sulfate PolyAcrylamide Gel Electrophoresis) and the phosphorylation status was confirmed by an anti-phospho-STAT5 antibody (Cell Signaling Technology, Catalog #9354, Danvers MA) or an anti-phospho-STAT3 antibody (Cell Signaling Technology, Catalog #9145, Danvers MA) using immunoblotting (See FIG. ..

    Article Title: STAT3 regulates NK and NKT cell differentiation through C-X3-C motif chemokine receptor 1  (CX3CR1) in hyper-IgE syndrome
    Article Snippet: .. Proteins were separated using 8% SDS-PAGE and then incubated with anti-STAT3 antibody (Cat#A22264, CST) and anti-Phospho-STAT3 antibody (Cat#9145S, CST). ..

    Polyacrylamide Gel Electrophoresis:

    Article Title: Peptides inhibiting gamma-c-cytokine activity and methods of use
    Article Snippet: .. The extracted cytoplasmic proteins were resolved using a standard SDS-PAGE (Sodium Dodecyl-Sulfate PolyAcrylamide Gel Electrophoresis) and the phosphorylation status was confirmed by an anti-phospho-STAT5 antibody (Cell Signaling Technology, Catalog #9354, Danvers MA) or an anti-phospho-STAT3 antibody (Cell Signaling Technology, Catalog #9145, Danvers MA) using immunoblotting (See FIG. ..

    Phospho-proteomics:

    Article Title: Peptides inhibiting gamma-c-cytokine activity and methods of use
    Article Snippet: .. The extracted cytoplasmic proteins were resolved using a standard SDS-PAGE (Sodium Dodecyl-Sulfate PolyAcrylamide Gel Electrophoresis) and the phosphorylation status was confirmed by an anti-phospho-STAT5 antibody (Cell Signaling Technology, Catalog #9354, Danvers MA) or an anti-phospho-STAT3 antibody (Cell Signaling Technology, Catalog #9145, Danvers MA) using immunoblotting (See FIG. ..

    Article Title: Apigenin regulates CCR5/JAK1/STAT1/MMPs signaling to alleviate secondary brain injury after intracerebral hemorrhage and its enhanced delivery via targeted nanoparticles
    Article Snippet: Different concentrations of apigenin (10 μM and 20 μM; Cat# A800500, Macklin, China) were added to the reaction system, which was maintained at 30 °C for 30 min. .. Reactions were terminated by adding 1× Laemmli buffer (Cat# 1610747, Bio-Rad, USA) and boiling at 95 °C for 5 min. Western blotting was performed using an anti-phospho-STAT3 antibody (Cat# 9145, Cell Signaling Technology, USA) to detect JAK2-mediated phosphorylation of STAT3 at Tyr705 [ ]. ..

    Article Title: Apigenin regulates CCR5/JAK1/STAT1/MMPs signaling to alleviate secondary brain injury after intracerebral hemorrhage and its enhanced delivery via targeted nanoparticles.
    Article Snippet: Different concentrations of apigenin (10 μM and 20 μM; Cat# A800500, Macklin, China) were added to the reaction system, which was maintained at 30 °C for 30 min. .. Reactions were terminated by adding 1× Laemmli buffer (Cat# 1610747, Bio-Rad, USA) and boiling at 95 °C for 5 min. Western blotting was performed using an anti-phospho-STAT3 antibody (Cat# 9145, Cell Signaling Technology, USA) to detect JAK2mediated phosphorylation of STAT3 at Tyr705 [29]. ..

    Western Blot:

    Article Title: Peptides inhibiting gamma-c-cytokine activity and methods of use
    Article Snippet: .. The extracted cytoplasmic proteins were resolved using a standard SDS-PAGE (Sodium Dodecyl-Sulfate PolyAcrylamide Gel Electrophoresis) and the phosphorylation status was confirmed by an anti-phospho-STAT5 antibody (Cell Signaling Technology, Catalog #9354, Danvers MA) or an anti-phospho-STAT3 antibody (Cell Signaling Technology, Catalog #9145, Danvers MA) using immunoblotting (See FIG. ..

    Article Title: Apigenin regulates CCR5/JAK1/STAT1/MMPs signaling to alleviate secondary brain injury after intracerebral hemorrhage and its enhanced delivery via targeted nanoparticles
    Article Snippet: Different concentrations of apigenin (10 μM and 20 μM; Cat# A800500, Macklin, China) were added to the reaction system, which was maintained at 30 °C for 30 min. .. Reactions were terminated by adding 1× Laemmli buffer (Cat# 1610747, Bio-Rad, USA) and boiling at 95 °C for 5 min. Western blotting was performed using an anti-phospho-STAT3 antibody (Cat# 9145, Cell Signaling Technology, USA) to detect JAK2-mediated phosphorylation of STAT3 at Tyr705 [ ]. ..

    Article Title: Apigenin regulates CCR5/JAK1/STAT1/MMPs signaling to alleviate secondary brain injury after intracerebral hemorrhage and its enhanced delivery via targeted nanoparticles.
    Article Snippet: Different concentrations of apigenin (10 μM and 20 μM; Cat# A800500, Macklin, China) were added to the reaction system, which was maintained at 30 °C for 30 min. .. Reactions were terminated by adding 1× Laemmli buffer (Cat# 1610747, Bio-Rad, USA) and boiling at 95 °C for 5 min. Western blotting was performed using an anti-phospho-STAT3 antibody (Cat# 9145, Cell Signaling Technology, USA) to detect JAK2mediated phosphorylation of STAT3 at Tyr705 [29]. ..

    Incubation:

    Article Title: Investigation of the pharmacological mechanisms of Denglao Qingguan decoction in inhibiting viral pneumonia through network pharmacology and in vitro laboratory validation
    Article Snippet: .. The primary antibodies including anti-Stat3 antibody (Stat3, cat# 4904S, CST, United States), anti-phospho-Stat3 antibody (p-Stat3, cat# 9145, CST, United States), anti-Akt antibody (Akt, cat# 4685, CST, United States), anti-phospho-Akt antibody (p-Akt, cat# 9217, CST, United States), anti-phospho-p44/42 MAPK antibody (p-Erk1/2, cat# 4370, CST, United States), anti-p44/42 MAPK antibody (Erk1/2, cat# 9120, CST, United States) or anti-β-Actin antibody (cat# 8457, CST, United States) were incubated overnight at 4°C, followed by the incubation with corresponding secondary antibodies (anti-rabbit IgG, cat# SA00001-2, proteintech, United States or anti-mouse IgG cat# SA00001-1, proteintech, United States) for 1 h. .. Statistical analysis was performed using Prism GraphPad 8 software.

    Article Title: STAT3 regulates NK and NKT cell differentiation through C-X3-C motif chemokine receptor 1  (CX3CR1) in hyper-IgE syndrome
    Article Snippet: .. Proteins were separated using 8% SDS-PAGE and then incubated with anti-STAT3 antibody (Cat#A22264, CST) and anti-Phospho-STAT3 antibody (Cat#9145S, CST). ..



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    Image Search Results


    Ovarian AGE–RAGE/STAT3/AKT1‐related protein expression and phosphorylation. (A) Representative Western blot bands for AGE, RAGE, STAT3, AKT1, phospho‐STAT3 (Ser727), phospho‐AKT (Ser473), and GAPDH in the Control, Model, HLWDD‐L, HLWDD‐M, HLWDD‐H, and Metformin groups. (B) Relative densitometric analysis of AGE/GAPDH, RAGE/GAPDH, STAT3/GAPDH, AKT1/GAPDH, p‐STAT3/STAT3, and p‐AKT/AKT1. ** p < 0.01 vs. Control; ## p < 0.01 vs. Model. Densitometric comparisons were based on independent biological replicates and analyzed as described in Methods.

    Journal: Chemistry & Biodiversity

    Article Title: Network Pharmacology and In Vivo Evaluation of Modified Huanglian Wendan Decoction in Polycystic Ovary Syndrome With Insulin Resistance: Association With AGE–RAGE‐Related Signaling

    doi: 10.1002/cbdv.71737

    Figure Lengend Snippet: Ovarian AGE–RAGE/STAT3/AKT1‐related protein expression and phosphorylation. (A) Representative Western blot bands for AGE, RAGE, STAT3, AKT1, phospho‐STAT3 (Ser727), phospho‐AKT (Ser473), and GAPDH in the Control, Model, HLWDD‐L, HLWDD‐M, HLWDD‐H, and Metformin groups. (B) Relative densitometric analysis of AGE/GAPDH, RAGE/GAPDH, STAT3/GAPDH, AKT1/GAPDH, p‐STAT3/STAT3, and p‐AKT/AKT1. ** p < 0.01 vs. Control; ## p < 0.01 vs. Model. Densitometric comparisons were based on independent biological replicates and analyzed as described in Methods.

    Article Snippet: Primary antibodies included AGE (A16422, ABclonal; 1:2000), RAGE (66833‐1‐Ig, Proteintech; 1:2000), STAT3 (60199‐1‐Ig, Proteintech; 1:1000), AKT1 (10176‐2‐AP, Proteintech; 1:2000), phospho‐STAT3 (Ser727; AP0715, ABclonal; 1:2000), phospho‐AKT (Ser473; 80455‐1‐RR, Proteintech; 1:1000), and GAPDH (60004‐1‐Ig, Proteintech; 1:20000).

    Techniques: Expressing, Phospho-proteomics, Western Blot, Control, Analysis

    KPF ameliorates placental pathological changes and oxidative stress in GDM rats. (A) HE staining was performed to evaluate pathological alterations in placental tissues. Magnification: 100×; scale bar: 200 μm. (B) PAS staining was performed to assess glycogen distribution and deposition in placental tissues. Magnification: 100×; scale bar: 200 μm. (C, D) DHE staining was performed to evaluate ROS accumulation in placental tissues. Magnification: 200×; scale bar: 20 μm. (E–I) Western blot analysis was performed to determine the protein expression levels of AIM2, p-STAT3, GPX4, and SLC7A11 in placental tissues. N = 3, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Physiology

    Article Title: Kaempferol ameliorates gestational diabetes mellitus by regulating STAT3-associated AIM2 inflammasome activation and ferroptotic injury in trophoblasts

    doi: 10.3389/fphys.2026.1857741

    Figure Lengend Snippet: KPF ameliorates placental pathological changes and oxidative stress in GDM rats. (A) HE staining was performed to evaluate pathological alterations in placental tissues. Magnification: 100×; scale bar: 200 μm. (B) PAS staining was performed to assess glycogen distribution and deposition in placental tissues. Magnification: 100×; scale bar: 200 μm. (C, D) DHE staining was performed to evaluate ROS accumulation in placental tissues. Magnification: 200×; scale bar: 20 μm. (E–I) Western blot analysis was performed to determine the protein expression levels of AIM2, p-STAT3, GPX4, and SLC7A11 in placental tissues. N = 3, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: Following blocking, the membranes were incubated overnight at 4°C with primary antibodies, including AIM2 (1:1000, catalog number ab93015, Abcam), Glutathione Peroxidase 4 (GPX4, 1:1000, 52455, Cell Signaling Technology, CST), solute carrier family 7 member 11 (SLC7A11, 1:1000, 23276, CST), phospho-STAT3 (p-STAT3, 1:1000, 9145, CST), STAT3 (1:1000, 12640, CST), pro-IL-1β (1:1000, 12703, CST), IL-1β (1:1000, ab283818, Abcam), cleaved caspase-1 (1:1000, 4199, CST), pro-caspase-1 (1:1000, 24232, CST), STAT1 (1:1000, 9172T, CST), phospho-STAT1 (p-STAT1, 1:1000, 9177S, CST), IRF1 (1:1000, 9172T, CST) and β-actin (1:1000, 4967S, CST).

    Techniques: H&E Stain, Staining, Western Blot, Analysis, Expressing

    KPF modulates trophoblast inflammatory responses and ferroptosis-related alterations through STAT3-associated signaling regulation. (A) Molecular docking analysis showing the potential interaction between KPF and STAT3 protein. (B, C) RT-qPCR analysis of STAT3 mRNA expression and transfection efficiency in HTR-8/SVneo cells. (D) CCK-8 assay was used to evaluate cell viability. (E, F) ELISA quantification of inflammatory cytokines IL-18 and TNF-α in cell supernatants. (G–L) Western blot analysis of AIM2, IL-1β, pro-IL-1β, GPX4, SLC7A11, cleaved caspase-1, and pro-caspase-1 protein expression in cells subjected to various treatments. (M–P) Western blot analysis of STAT3-associated changes in STAT3, GPX4, and SLC7A11 protein expression in cells subjected to various treatments. N = 3, not significant, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Physiology

    Article Title: Kaempferol ameliorates gestational diabetes mellitus by regulating STAT3-associated AIM2 inflammasome activation and ferroptotic injury in trophoblasts

    doi: 10.3389/fphys.2026.1857741

    Figure Lengend Snippet: KPF modulates trophoblast inflammatory responses and ferroptosis-related alterations through STAT3-associated signaling regulation. (A) Molecular docking analysis showing the potential interaction between KPF and STAT3 protein. (B, C) RT-qPCR analysis of STAT3 mRNA expression and transfection efficiency in HTR-8/SVneo cells. (D) CCK-8 assay was used to evaluate cell viability. (E, F) ELISA quantification of inflammatory cytokines IL-18 and TNF-α in cell supernatants. (G–L) Western blot analysis of AIM2, IL-1β, pro-IL-1β, GPX4, SLC7A11, cleaved caspase-1, and pro-caspase-1 protein expression in cells subjected to various treatments. (M–P) Western blot analysis of STAT3-associated changes in STAT3, GPX4, and SLC7A11 protein expression in cells subjected to various treatments. N = 3, not significant, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: Following blocking, the membranes were incubated overnight at 4°C with primary antibodies, including AIM2 (1:1000, catalog number ab93015, Abcam), Glutathione Peroxidase 4 (GPX4, 1:1000, 52455, Cell Signaling Technology, CST), solute carrier family 7 member 11 (SLC7A11, 1:1000, 23276, CST), phospho-STAT3 (p-STAT3, 1:1000, 9145, CST), STAT3 (1:1000, 12640, CST), pro-IL-1β (1:1000, 12703, CST), IL-1β (1:1000, ab283818, Abcam), cleaved caspase-1 (1:1000, 4199, CST), pro-caspase-1 (1:1000, 24232, CST), STAT1 (1:1000, 9172T, CST), phospho-STAT1 (p-STAT1, 1:1000, 9177S, CST), IRF1 (1:1000, 9172T, CST) and β-actin (1:1000, 4967S, CST).

    Techniques: Docking Assay, Analysis, Quantitative RT-PCR, Expressing, Transfection, CCK-8 Assay, Enzyme-linked Immunosorbent Assay, Western Blot

    STAT3-associated changes in STAT1/IRF1 signaling and AIM2 expression in HG-stimulated trophoblast cells. (A, B) RT-qPCR was performed to assess STAT3 knockdown efficiency and AIM2 mRNA expression changes in HTR-8/SVneo cells subjected to different treatments. (C–F) Western blot analysis was performed to evaluate the expression levels of p-STAT1, STAT1, IRF1, and AIM2 proteins under different experimental conditions. N = 3, not significant, ** P <0.01, *** P <0.001.

    Journal: Frontiers in Physiology

    Article Title: Kaempferol ameliorates gestational diabetes mellitus by regulating STAT3-associated AIM2 inflammasome activation and ferroptotic injury in trophoblasts

    doi: 10.3389/fphys.2026.1857741

    Figure Lengend Snippet: STAT3-associated changes in STAT1/IRF1 signaling and AIM2 expression in HG-stimulated trophoblast cells. (A, B) RT-qPCR was performed to assess STAT3 knockdown efficiency and AIM2 mRNA expression changes in HTR-8/SVneo cells subjected to different treatments. (C–F) Western blot analysis was performed to evaluate the expression levels of p-STAT1, STAT1, IRF1, and AIM2 proteins under different experimental conditions. N = 3, not significant, ** P <0.01, *** P <0.001.

    Article Snippet: Following blocking, the membranes were incubated overnight at 4°C with primary antibodies, including AIM2 (1:1000, catalog number ab93015, Abcam), Glutathione Peroxidase 4 (GPX4, 1:1000, 52455, Cell Signaling Technology, CST), solute carrier family 7 member 11 (SLC7A11, 1:1000, 23276, CST), phospho-STAT3 (p-STAT3, 1:1000, 9145, CST), STAT3 (1:1000, 12640, CST), pro-IL-1β (1:1000, 12703, CST), IL-1β (1:1000, ab283818, Abcam), cleaved caspase-1 (1:1000, 4199, CST), pro-caspase-1 (1:1000, 24232, CST), STAT1 (1:1000, 9172T, CST), phospho-STAT1 (p-STAT1, 1:1000, 9177S, CST), IRF1 (1:1000, 9172T, CST) and β-actin (1:1000, 4967S, CST).

    Techniques: Expressing, Quantitative RT-PCR, Knockdown, Western Blot, Analysis

    Journal: Cell Reports Medicine

    Article Title: A biomimetic hybrid membrane vesicle nanoplatform attenuates tendinopathy through neuroinflammation modulation and tendon regeneration

    doi: 10.1016/j.xcrm.2026.102937

    Figure Lengend Snippet:

    Article Snippet: Rabbit Polyclonal anti-p-STAT3 , ABclonal , Cat# AP0705; RRID: AB_2863810.

    Techniques: Recombinant, Lysis, Hydroxyproline Assay, Enzyme-linked Immunosorbent Assay, Isolation, SYBR Green Assay, Bicinchoninic Acid Protein Assay, Staining, Software