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Cell Signaling Technology Inc phospho pi3k p85 tyr458
ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, <t>PI3K/AKT</t> signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.
Phospho Pi3k P85 Tyr458, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc p pi3k
ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, <t>PI3K/AKT</t> signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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MedChemExpress rabbit anti p pi3k
ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, <t>PI3K/AKT</t> signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.
Rabbit Anti P Pi3k, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc anti phospho pi3k p85
ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, <t>PI3K/AKT</t> signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.
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MedChemExpress rabbit p pi3k
Tryptophanol treatment alleviated POF symptoms by inhibiting <t>PI3K/AKT</t> and MAPK pathways. A Experimental scheme. B Estrus status of mice ( n = 8). C Body weights of mice ( n = 8). D Ovary weights of mice ( n = 8). E Representative Ovary from the Control, the POF and the NCG groups mice with H&E and IHC staining. H&E scale bar = 200 μm; IHC scale bar = 100 μm. F Quantification of primordial, primary, secondary, antral follicles, corpora lutea and corpora atretica per ovary. n = 3 ovaries per each condition. Levels of FSH ( G ), LH ( H ), E 2 ( I ) in mouse serum ( n = 6). Levels of ROS ( J ), MDA ( K ), SOD ( L ), GSH-Px ( M ) in mouse ovaries ( n = 3–4). N Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). O Litter sizes of mice ( n = 3). Data presented as the mean ± SD, statistical significance was determined using one-way or two-way ANOVA. * p < 0.05, ** p < 0.01. *** p < 0.001. Different lowercase letters indicate significant differences ( p < 0.05)
Rabbit P Pi3k, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/phospho+pi3k+p85/Phospho-PI3+Kinase+p85%2Fp55+(Tyr467%2FTyr199)+Antibody/pmc13459312-125-74-76
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Cell Signaling Technology Inc phospho pi3k p85 tyr458 p55 tyr199
Tryptophanol treatment alleviated POF symptoms by inhibiting <t>PI3K/AKT</t> and MAPK pathways. A Experimental scheme. B Estrus status of mice ( n = 8). C Body weights of mice ( n = 8). D Ovary weights of mice ( n = 8). E Representative Ovary from the Control, the POF and the NCG groups mice with H&E and IHC staining. H&E scale bar = 200 μm; IHC scale bar = 100 μm. F Quantification of primordial, primary, secondary, antral follicles, corpora lutea and corpora atretica per ovary. n = 3 ovaries per each condition. Levels of FSH ( G ), LH ( H ), E 2 ( I ) in mouse serum ( n = 6). Levels of ROS ( J ), MDA ( K ), SOD ( L ), GSH-Px ( M ) in mouse ovaries ( n = 3–4). N Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). O Litter sizes of mice ( n = 3). Data presented as the mean ± SD, statistical significance was determined using one-way or two-way ANOVA. * p < 0.05, ** p < 0.01. *** p < 0.001. Different lowercase letters indicate significant differences ( p < 0.05)
Phospho Pi3k P85 Tyr458 P55 Tyr199, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, PI3K/AKT signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.

Journal: Cancer Biology & Therapy

Article Title: ARHGAP40 suppresses clear cell renal cell carcinoma progression and is associated with altered glutamine-related metabolism and redox balance

doi: 10.1080/15384047.2026.2746137

Figure Lengend Snippet: ARHGAP40 associates with RhoA and is accompanied by reduced RhoA activity, PI3K/AKT signaling, and altered glutamine-related/redox measures. (A) Flag-based co-immunoprecipitation showing association of ARHGAP40 with RhoA. (B) Endogenous immunoprecipitation of RhoA followed by immunoblotting for ARHGAP40. (C) RhoA activity assay using a conformation-specific anti-RhoA-GTP antibody, with representative GTP-RhoA and total RhoA blots and quantification of the GTP-RhoA/total RhoA ratio. (D) Representative western blots and densitometric analyzes of p -AKT/AKT and p -PI3K/PI3K. (E) Intracellular glutamate levels. (F) Intracellular glutamine levels. (G) GSH/GSSG ratios. (H) Representative ROS flow-cytometry histograms and mean fluorescence intensity. Quantitative analyzes used n = 3 independent biological replicates and are shown as mean ± SEM. Two-group comparisons were performed using two-tailed Student's t-test. * P < 0.05, ** P < 0.01, *** P < 0.001.

Article Snippet: Membranes were blocked with 5% non-fat milk in TBST and incubated overnight at 4 °C with primary antibodies: β -actin (CST, 4970, 1:1000), ARHGAP40 (MyBioSource, MBS9215052, 1:1000), AKT (CST, 9272, 1:2000), phospho-AKT Ser473 (CST, 4060, 1:1000), PI3K p85 (CST, 4257, 1:1000), phospho-PI3K p85 Tyr458 (CST, 4228, 1:1000), RhoA (CST, 2117, 1:2000), E-cadherin (CST, 3195, 1:2000), N -cadherin (CST, 4061, 1:2000), and vimentin (CST, 5741, 1:2000).

Techniques: Activity Assay, Co-Immunoprecipitation Assay, Immunoprecipitation, Western Blot, Flow Cytometry, Fluorescence, Two Tailed Test

Tryptophanol treatment alleviated POF symptoms by inhibiting PI3K/AKT and MAPK pathways. A Experimental scheme. B Estrus status of mice ( n = 8). C Body weights of mice ( n = 8). D Ovary weights of mice ( n = 8). E Representative Ovary from the Control, the POF and the NCG groups mice with H&E and IHC staining. H&E scale bar = 200 μm; IHC scale bar = 100 μm. F Quantification of primordial, primary, secondary, antral follicles, corpora lutea and corpora atretica per ovary. n = 3 ovaries per each condition. Levels of FSH ( G ), LH ( H ), E 2 ( I ) in mouse serum ( n = 6). Levels of ROS ( J ), MDA ( K ), SOD ( L ), GSH-Px ( M ) in mouse ovaries ( n = 3–4). N Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). O Litter sizes of mice ( n = 3). Data presented as the mean ± SD, statistical significance was determined using one-way or two-way ANOVA. * p < 0.05, ** p < 0.01. *** p < 0.001. Different lowercase letters indicate significant differences ( p < 0.05)

Journal: Journal of Ovarian Research

Article Title: Gut microbiota-derived Tryptophanol driven by N-Carbamylglutamate alleviates premature ovarian failure through inhibiting oxidative stress

doi: 10.1186/s13048-026-02152-4

Figure Lengend Snippet: Tryptophanol treatment alleviated POF symptoms by inhibiting PI3K/AKT and MAPK pathways. A Experimental scheme. B Estrus status of mice ( n = 8). C Body weights of mice ( n = 8). D Ovary weights of mice ( n = 8). E Representative Ovary from the Control, the POF and the NCG groups mice with H&E and IHC staining. H&E scale bar = 200 μm; IHC scale bar = 100 μm. F Quantification of primordial, primary, secondary, antral follicles, corpora lutea and corpora atretica per ovary. n = 3 ovaries per each condition. Levels of FSH ( G ), LH ( H ), E 2 ( I ) in mouse serum ( n = 6). Levels of ROS ( J ), MDA ( K ), SOD ( L ), GSH-Px ( M ) in mouse ovaries ( n = 3–4). N Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). O Litter sizes of mice ( n = 3). Data presented as the mean ± SD, statistical significance was determined using one-way or two-way ANOVA. * p < 0.05, ** p < 0.01. *** p < 0.001. Different lowercase letters indicate significant differences ( p < 0.05)

Article Snippet: The membrane was blocked with 5% bovine serum albumin (BSA; Sigma) for 1 h at room temperature, followed by overnight incubation at 4 °C with the primary antibodies: rabbit Cleaved caspase 3 (MCE, HY- P80623 , 1:800), rabbit BAX (Bioworld, BS61098, 1:800), rabbit BCL2 (Bioworld, BS1511, 1:800), rabbit ERK1/2 (Bioworld, BS90472, 1:1,000), rabbit p-ERK1/2 (Bioworld, BS4621P, 1:1,000), rabbit p38 (Bioworld, BS4635, 1:1,000), rabbit p-p38 (Bioworld, BS4766, 1:1,000), rabbit PI3K (MCE, HY- P80867 , 1:1,000); rabbit p-PI3K (MCE, HY- P80846 , 1:1,000), rabbit AKT (Bioworld, MB3288 1:1,000); rabbit p-AKT (Bioworld, BS4007 1:1,000); rabbit IL-6 (Abclonal, A0286, 1:800), rabbit IL-1β (MCE, HY- P80720 , 1:1,000), rabbit Occludin (Abclonal, A2601, 1:1,000); rabbit ZO-1 (Bioworld, BS71522, 1:1,000); rabbit GPX4 (MCE, HY- P80450 , 1:1,000); mouse GAPDH (Bioworld, MB001, 1:1,000); rabbit SOD2 (Bioworld, BS6734, 1:1,000).

Techniques: Control, Immunohistochemistry, Western Blot

Tryptophanol treatment alleviated POF by inhibiting PI3K/AKT and MAPK pathways in vitro . A Experimental scheme. B Different concentrations of Cy on GCs viability was assessed by CCK8 assay. C and E Different concentrations of Trp on GCs viability was assessed by CCK8 assay. D The effect of Trp on GCs cell viability following Cy treatment. The control and treatment groups were stained with DCFH-DA, the cells were washed and examined by fluorescence microscopy. Scale bar = 50 μm. F The fluorescence intensity of ROS in mouse GCs. G The level of MDA in mouse GCs. H Flow cytometry apoptosis analysis graph and cell death rate in different groups. The level of SOD ( I ), GSH-Px ( J ), and E 2 ( K ) in mouse GCs. ( L ) Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). All values are presented as the mean ± SD ( n = 3). Different lowercase letters indicate significant differences compared to the control group ( p < 0.05)

Journal: Journal of Ovarian Research

Article Title: Gut microbiota-derived Tryptophanol driven by N-Carbamylglutamate alleviates premature ovarian failure through inhibiting oxidative stress

doi: 10.1186/s13048-026-02152-4

Figure Lengend Snippet: Tryptophanol treatment alleviated POF by inhibiting PI3K/AKT and MAPK pathways in vitro . A Experimental scheme. B Different concentrations of Cy on GCs viability was assessed by CCK8 assay. C and E Different concentrations of Trp on GCs viability was assessed by CCK8 assay. D The effect of Trp on GCs cell viability following Cy treatment. The control and treatment groups were stained with DCFH-DA, the cells were washed and examined by fluorescence microscopy. Scale bar = 50 μm. F The fluorescence intensity of ROS in mouse GCs. G The level of MDA in mouse GCs. H Flow cytometry apoptosis analysis graph and cell death rate in different groups. The level of SOD ( I ), GSH-Px ( J ), and E 2 ( K ) in mouse GCs. ( L ) Western blotting ( a ) and quantitative ( b ) analysis of proteins ( n = 3). All values are presented as the mean ± SD ( n = 3). Different lowercase letters indicate significant differences compared to the control group ( p < 0.05)

Article Snippet: The membrane was blocked with 5% bovine serum albumin (BSA; Sigma) for 1 h at room temperature, followed by overnight incubation at 4 °C with the primary antibodies: rabbit Cleaved caspase 3 (MCE, HY- P80623 , 1:800), rabbit BAX (Bioworld, BS61098, 1:800), rabbit BCL2 (Bioworld, BS1511, 1:800), rabbit ERK1/2 (Bioworld, BS90472, 1:1,000), rabbit p-ERK1/2 (Bioworld, BS4621P, 1:1,000), rabbit p38 (Bioworld, BS4635, 1:1,000), rabbit p-p38 (Bioworld, BS4766, 1:1,000), rabbit PI3K (MCE, HY- P80867 , 1:1,000); rabbit p-PI3K (MCE, HY- P80846 , 1:1,000), rabbit AKT (Bioworld, MB3288 1:1,000); rabbit p-AKT (Bioworld, BS4007 1:1,000); rabbit IL-6 (Abclonal, A0286, 1:800), rabbit IL-1β (MCE, HY- P80720 , 1:1,000), rabbit Occludin (Abclonal, A2601, 1:1,000); rabbit ZO-1 (Bioworld, BS71522, 1:1,000); rabbit GPX4 (MCE, HY- P80450 , 1:1,000); mouse GAPDH (Bioworld, MB001, 1:1,000); rabbit SOD2 (Bioworld, BS6734, 1:1,000).

Techniques: In Vitro, CCK-8 Assay, Control, Staining, Fluorescence, Microscopy, Flow Cytometry, Western Blot