pathscan akt signaling antibody array kit  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc pathscan akt signaling antibody array kit
    Pathscan Akt Signaling Antibody Array Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    pathscan akt signaling antibody array kit  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc pathscan akt signaling antibody array kit
    Pathscan Akt Signaling Antibody Array Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    thr308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc thr308
    Thr308, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    phospho akt thr308  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt thr308
    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt <t>(Thr308)</t> and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.
    Phospho Akt Thr308, supplied by Cell Signaling Technology Inc, 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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    Average 94 stars, based on 1 article reviews
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    Images

    1) Product Images from "Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis"

    Article Title: Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0035685

    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.
    Figure Legend Snippet: Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Techniques Used:

    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), MCP-1 or MCP-1 + PI 3-Kγ inhibitor for 24 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.
    Figure Legend Snippet: Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), MCP-1 or MCP-1 + PI 3-Kγ inhibitor for 24 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Techniques Used:

    Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), conditioned media (CM) or ERK 1/2 inhibitor for 6 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.
    Figure Legend Snippet: Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), conditioned media (CM) or ERK 1/2 inhibitor for 6 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Techniques Used:

    p pkb  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p pkb
    Used antibodies in Western blot experiments.
    P Pkb, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/p pkb/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    p pkb - by Bioz Stars, 2023-03
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    1) Product Images from "Regenerative and fibrotic pathways in canine hepatic portosystemic shunt and portal vein hypoplasia, new models for clinical hepatocyte growth factor treatment"

    Article Title: Regenerative and fibrotic pathways in canine hepatic portosystemic shunt and portal vein hypoplasia, new models for clinical hepatocyte growth factor treatment

    Journal: Comparative Hepatology

    doi: 10.1186/1476-5926-4-7

    Used antibodies in Western blot experiments.
    Figure Legend Snippet: Used antibodies in Western blot experiments.

    Techniques Used: Western Blot

    phospho akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt
    (A) Western blotting demonstrated that levels of phospho-Erk1/2 <t>and</t> <t>phospho-p38</t> were both increased in cultured BMSCs from MT mice. There was, however, no change in <t>phospho-AKT.</t> (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    Phospho Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho akt/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    phospho akt - by Bioz Stars, 2023-03
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    1) Product Images from "A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation"

    Article Title: A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0087311

    (A) Western blotting demonstrated that levels of phospho-Erk1/2 and phospho-p38 were both increased in cultured BMSCs from MT mice. There was, however, no change in phospho-AKT. (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    Figure Legend Snippet: (A) Western blotting demonstrated that levels of phospho-Erk1/2 and phospho-p38 were both increased in cultured BMSCs from MT mice. There was, however, no change in phospho-AKT. (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)

    Techniques Used: Western Blot, Cell Culture, Expressing, Inhibition, Mutagenesis

    pi3k akt signaling  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc pi3k akt signaling
    Pi3k Akt Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pi3k akt signaling/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    98/100 stars

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    p13k akt signaling pathway  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p13k akt signaling pathway
    P13k Akt Signaling Pathway, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/p13k akt signaling pathway/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    98/100 stars

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    pi3k akt signaling pathway  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc pi3k akt signaling pathway
    Pi3k Akt Signaling Pathway, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/pi3k akt signaling pathway/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    phospho akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho akt
    Analysis of anti-tumor drug effects on the mTOR signaling pathway. Western blot results show the HIN1, mTOR, phosphorylation of mTOR (p-mTOR), Rictor, phosphorylation of Rictor (p-Rictor), <t>AKT,</t> phosphorylation of AKT (p-AKT) <t>(Thr308),</t> p-AKT (Ser473), and GAPDH in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001. The numbers in the immunoblot represent the relative folds of HIN-1, p-mTOR, p-Rictor, p-AKT (Thr308), and p-AKT (Ser473) in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001 compared to the control group in ES2 cells without treatment. The numbers in the immunoblot were calculated as target protein density/target protein+GAPDH density and set the control group in ES2 cells without treatment as 1.
    Phospho Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Everolimus combined with 5-aza-2-deoxycytidine generated potent anti-tumor effects on ovarian clear cell cancer stem-like/spheroid cells by inhibiting the COL6A3-AKT-mTOR pathway"

    Article Title: Everolimus combined with 5-aza-2-deoxycytidine generated potent anti-tumor effects on ovarian clear cell cancer stem-like/spheroid cells by inhibiting the COL6A3-AKT-mTOR pathway

    Journal: American Journal of Cancer Research

    doi:

    Analysis of anti-tumor drug effects on the mTOR signaling pathway. Western blot results show the HIN1, mTOR, phosphorylation of mTOR (p-mTOR), Rictor, phosphorylation of Rictor (p-Rictor), AKT, phosphorylation of AKT (p-AKT) (Thr308), p-AKT (Ser473), and GAPDH in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001. The numbers in the immunoblot represent the relative folds of HIN-1, p-mTOR, p-Rictor, p-AKT (Thr308), and p-AKT (Ser473) in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001 compared to the control group in ES2 cells without treatment. The numbers in the immunoblot were calculated as target protein density/target protein+GAPDH density and set the control group in ES2 cells without treatment as 1.
    Figure Legend Snippet: Analysis of anti-tumor drug effects on the mTOR signaling pathway. Western blot results show the HIN1, mTOR, phosphorylation of mTOR (p-mTOR), Rictor, phosphorylation of Rictor (p-Rictor), AKT, phosphorylation of AKT (p-AKT) (Thr308), p-AKT (Ser473), and GAPDH in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001. The numbers in the immunoblot represent the relative folds of HIN-1, p-mTOR, p-Rictor, p-AKT (Thr308), and p-AKT (Ser473) in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001 compared to the control group in ES2 cells without treatment. The numbers in the immunoblot were calculated as target protein density/target protein+GAPDH density and set the control group in ES2 cells without treatment as 1.

    Techniques Used: Western Blot

    Statistic analysis of anti-tumor drug effects on the mTOR signaling pathway. Statistic analysis results show the relative folds of HIN1, phosphorylation of mTOR (p-mTOR), phosphorylation of Rictor (p-Rictor), phosphorylation of AKT (p-AKT) (Thr308), and p-AKT (Ser473) in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001.
    Figure Legend Snippet: Statistic analysis of anti-tumor drug effects on the mTOR signaling pathway. Statistic analysis results show the relative folds of HIN1, phosphorylation of mTOR (p-mTOR), phosphorylation of Rictor (p-Rictor), phosphorylation of AKT (p-AKT) (Thr308), and p-AKT (Ser473) in ES2 cells, ES2 tumorspheres (TS), ES2TR160 cells, and ES2TR160 TS treated with 5-aza-dC, RAD001, or 5-aza-dC combined with RAD001.

    Techniques Used:

    Effects of anti-tumor drugs on phosphorylation of mTOR-pathway enzymes. Western blot analysis shows the COL6A3, mTOR, phosphorylation of mTOR (p-mTOR), Rictor, phosphorylation of Rictor (p-Rictor), AKT, phosphorylation of AKT (p-AKT) (Thr308), and p-AKT (Ser473) in COL6A3-silenced ES2 and ES2TR160 tumorspheres (TS), treated without (-) or with 5-Aza-dC, RAD001, or 5-Aza-dC combined with RAD001. The blots were cropped from the original blots. The numbers in the immunoblot represent the relative folds of COL6A3, p-mTOR, p-Rictor, p-AKT (Thr308), and p-AKT (Ser473) in COL6A3-silenced ES2 and ES2TR160 TS, treated without (-) or with 5-Aza-dC, RAD001, or 5-Aza-dC combined with RAD001 compared to ES2 and ES2TR160 TS. The numbers in the immunoblot were calculated as target protein density/target protein+GAPDH density and set the control group in ES2 and ES2TR160 TS without treatment as 1.
    Figure Legend Snippet: Effects of anti-tumor drugs on phosphorylation of mTOR-pathway enzymes. Western blot analysis shows the COL6A3, mTOR, phosphorylation of mTOR (p-mTOR), Rictor, phosphorylation of Rictor (p-Rictor), AKT, phosphorylation of AKT (p-AKT) (Thr308), and p-AKT (Ser473) in COL6A3-silenced ES2 and ES2TR160 tumorspheres (TS), treated without (-) or with 5-Aza-dC, RAD001, or 5-Aza-dC combined with RAD001. The blots were cropped from the original blots. The numbers in the immunoblot represent the relative folds of COL6A3, p-mTOR, p-Rictor, p-AKT (Thr308), and p-AKT (Ser473) in COL6A3-silenced ES2 and ES2TR160 TS, treated without (-) or with 5-Aza-dC, RAD001, or 5-Aza-dC combined with RAD001 compared to ES2 and ES2TR160 TS. The numbers in the immunoblot were calculated as target protein density/target protein+GAPDH density and set the control group in ES2 and ES2TR160 TS without treatment as 1.

    Techniques Used: Western Blot

    akt  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc akt

    Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/akt/product/Cell Signaling Technology Inc
    Average 98 stars, based on 1 article reviews
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    akt - by Bioz Stars, 2023-03
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    1) Product Images from "Betacellulin promotes tumor development and EGFR mutant lung cancer growth by stimulating the EGFR pathway and suppressing apoptosis"

    Article Title: Betacellulin promotes tumor development and EGFR mutant lung cancer growth by stimulating the EGFR pathway and suppressing apoptosis

    Journal: iScience

    doi: 10.1016/j.isci.2022.104211


    Figure Legend Snippet:

    Techniques Used: Neutralization, Microarray, Mutagenesis, Recombinant, Transfection, Staining, Plasmid Preparation, shRNA, Software

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    Cell Signaling Technology Inc pathscan akt signaling antibody array kit
    Pathscan Akt Signaling Antibody Array Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc phospho akt thr308
    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt <t>(Thr308)</t> and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.
    Phospho Akt Thr308, supplied by Cell Signaling Technology Inc, 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 p pkb
    Used antibodies in Western blot experiments.
    P Pkb, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc phospho akt
    (A) Western blotting demonstrated that levels of phospho-Erk1/2 <t>and</t> <t>phospho-p38</t> were both increased in cultured BMSCs from MT mice. There was, however, no change in <t>phospho-AKT.</t> (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    Phospho Akt, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc pi3k akt signaling
    (A) Western blotting demonstrated that levels of phospho-Erk1/2 <t>and</t> <t>phospho-p38</t> were both increased in cultured BMSCs from MT mice. There was, however, no change in <t>phospho-AKT.</t> (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    Pi3k Akt Signaling, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Western blotting demonstrated that levels of phospho-Erk1/2 <t>and</t> <t>phospho-p38</t> were both increased in cultured BMSCs from MT mice. There was, however, no change in <t>phospho-AKT.</t> (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    P13k Akt Signaling Pathway, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Western blotting demonstrated that levels of phospho-Erk1/2 <t>and</t> <t>phospho-p38</t> were both increased in cultured BMSCs from MT mice. There was, however, no change in <t>phospho-AKT.</t> (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)
    Pi3k Akt Signaling Pathway, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Journal: PLoS ONE

    Article Title: Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis

    doi: 10.1371/journal.pone.0035685

    Figure Lengend Snippet: Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes) or conditioned media (CM) for 24 hours under hypoxic conditions. Data calculated as a mean percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Article Snippet: An ELISA was used to detect changes in the levels of total-Bad, phospho-Bad (Ser112), total-Akt, phospho-Akt (Ser473), phospho-Akt (Thr308) and ERK 1/2 using PathScan Sandwich ELISA Kits (Cell Signaling Technology #7162, 7182, 7170, 7160, 7252) or a STAR ERK 1/2 ELISA kit (Upstate #17-463).

    Techniques:

    Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), MCP-1 or MCP-1 + PI 3-Kγ inhibitor for 24 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Journal: PLoS ONE

    Article Title: Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis

    doi: 10.1371/journal.pone.0035685

    Figure Lengend Snippet: Changes in caspase-3, phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), MCP-1 or MCP-1 + PI 3-Kγ inhibitor for 24 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Article Snippet: An ELISA was used to detect changes in the levels of total-Bad, phospho-Bad (Ser112), total-Akt, phospho-Akt (Ser473), phospho-Akt (Thr308) and ERK 1/2 using PathScan Sandwich ELISA Kits (Cell Signaling Technology #7162, 7182, 7170, 7160, 7252) or a STAR ERK 1/2 ELISA kit (Upstate #17-463).

    Techniques:

    Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), conditioned media (CM) or ERK 1/2 inhibitor for 6 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Journal: PLoS ONE

    Article Title: Mesenchymal Stem Cells Secrete Multiple Cytokines That Promote Angiogenesis and Have Contrasting Effects on Chemotaxis and Apoptosis

    doi: 10.1371/journal.pone.0035685

    Figure Lengend Snippet: Changes in phospho-Akt (Ser473), phospho-Akt (Thr308) and phospho-Bad (Ser112) in H9c2 cells treated with Mesencult (Mes), conditioned media (CM) or ERK 1/2 inhibitor for 6 hours under hypoxic conditions. Data calculated as a percent of Mesencult (control) treated cultures ± SE. a = p<0.05, b = p<0.01 compared to controls.

    Article Snippet: An ELISA was used to detect changes in the levels of total-Bad, phospho-Bad (Ser112), total-Akt, phospho-Akt (Ser473), phospho-Akt (Thr308) and ERK 1/2 using PathScan Sandwich ELISA Kits (Cell Signaling Technology #7162, 7182, 7170, 7160, 7252) or a STAR ERK 1/2 ELISA kit (Upstate #17-463).

    Techniques:

    Used antibodies in Western blot experiments.

    Journal: Comparative Hepatology

    Article Title: Regenerative and fibrotic pathways in canine hepatic portosystemic shunt and portal vein hypoplasia, new models for clinical hepatocyte growth factor treatment

    doi: 10.1186/1476-5926-4-7

    Figure Lengend Snippet: Used antibodies in Western blot experiments.

    Article Snippet: p-PKB (Thr 308) , 60 , 1:1,000 , Cell-Signaling , Anti-mouse HRP , 1:20,000.

    Techniques: Western Blot

    (A) Western blotting demonstrated that levels of phospho-Erk1/2 and phospho-p38 were both increased in cultured BMSCs from MT mice. There was, however, no change in phospho-AKT. (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)

    Journal: PLoS ONE

    Article Title: A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation

    doi: 10.1371/journal.pone.0087311

    Figure Lengend Snippet: (A) Western blotting demonstrated that levels of phospho-Erk1/2 and phospho-p38 were both increased in cultured BMSCs from MT mice. There was, however, no change in phospho-AKT. (B, C) The p38 and Erk1/2 pathways were inhibited by SB203580 and PD98059, respectively. (D–G) Relative expression of genes in BMSCs treated with SB203580 or PD98059 for 21 days. The expression levels of Col2 , Col10 , OC , and OP were significantly increased in both WT and MT BMSCs treated with SB203580; however, only OC and OP were increased after PD98059 treatment. (Student's t-test, * P <0.05, ** P <0.01 versus untreated BMSCs, # P <0.05 versus wild-type BMSCs.). (H) Inhibition of p38 and Erk1/2 pathway by SB203580 and PD98059 rescued the growth retardation in cultured mutant tibia bones. The white double-headed arrows represent the total length (TL) and ossified tissue length (OL). (I) Percentage increases in TL and OL of phalange bones after culture for 7 days. (Student's t-test, # P<0.05 versus wild-type *P<0.05 versus mutant type.)

    Article Snippet: Blotted protein was probed with antibodies specific to phospho-p38 and p38, phospho-Erk1/2 and Erk1/2, phospho-AKT, and AKT (Cell Signaling Technology, USA) as described previously .

    Techniques: Western Blot, Cell Culture, Expressing, Inhibition, Mutagenesis

    Journal: iScience

    Article Title: Betacellulin promotes tumor development and EGFR mutant lung cancer growth by stimulating the EGFR pathway and suppressing apoptosis

    doi: 10.1016/j.isci.2022.104211

    Figure Lengend Snippet:

    Article Snippet: Akt , Cell Signaling Technology , Cat# 9272S RRID: AB_329827.

    Techniques: Neutralization, Microarray, Mutagenesis, Recombinant, Transfection, Staining, Plasmid Preparation, shRNA, Software