bad  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc bad
    Bad, 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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    bad  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc bad
    Bad, 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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    bad d24a9  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc bad d24a9
    Bad D24a9, 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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    phospho bad ser136  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho bad ser136
    Antibodies used in immunofluorescence and western blot.
    Phospho Bad Ser136, 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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    1) Product Images from "Post-Injury Treatment with 7,8-Dihydroxyflavone, a TrkB Receptor Agonist, Protects against Experimental Traumatic Brain Injury via PI3K/Akt Signaling"

    Article Title: Post-Injury Treatment with 7,8-Dihydroxyflavone, a TrkB Receptor Agonist, Protects against Experimental Traumatic Brain Injury via PI3K/Akt Signaling

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0113397

    Antibodies used in immunofluorescence and western blot.
    Figure Legend Snippet: Antibodies used in immunofluorescence and western blot.

    Techniques Used: Immunofluorescence, Western Blot

    bad  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc bad
    JNK activation is required for spautin-1-induced <t>BAD</t> expression. (A) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) for 24 hours. (B, C) Indicated cells were treated with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM), CC-401 (100 nM), SB203580 (1 uM), SB239063 (100 nM), SCH772984 (100 nM), and LY3214996 (50 nM) for 24 hours. Bad mRNA and cell viability were assayed (n = 3, *p < 0.05, unpaired t-test). (D) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM) or CC-401 (100 nM) for 24 hours. (E) Q-PCR analysis of Jun gene expression in indicated Jun knockdown cancer cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test). (F-I) Knockdown of Jun inhibited spautin-1-(10µM) induced Bad mRNA expression (F), cell death (G), Bad promoter activity (H), <t>and</t> <t>CASP3</t> activity (I) in indicated cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test).
    Bad, 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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    1) Product Images from "TFAM is a novel mediator of immunogenic cancer cell death"

    Article Title: TFAM is a novel mediator of immunogenic cancer cell death

    Journal: Oncoimmunology

    doi: 10.1080/2162402X.2018.1431086

    JNK activation is required for spautin-1-induced BAD expression. (A) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) for 24 hours. (B, C) Indicated cells were treated with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM), CC-401 (100 nM), SB203580 (1 uM), SB239063 (100 nM), SCH772984 (100 nM), and LY3214996 (50 nM) for 24 hours. Bad mRNA and cell viability were assayed (n = 3, *p < 0.05, unpaired t-test). (D) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM) or CC-401 (100 nM) for 24 hours. (E) Q-PCR analysis of Jun gene expression in indicated Jun knockdown cancer cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test). (F-I) Knockdown of Jun inhibited spautin-1-(10µM) induced Bad mRNA expression (F), cell death (G), Bad promoter activity (H), and CASP3 activity (I) in indicated cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test).
    Figure Legend Snippet: JNK activation is required for spautin-1-induced BAD expression. (A) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) for 24 hours. (B, C) Indicated cells were treated with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM), CC-401 (100 nM), SB203580 (1 uM), SB239063 (100 nM), SCH772984 (100 nM), and LY3214996 (50 nM) for 24 hours. Bad mRNA and cell viability were assayed (n = 3, *p < 0.05, unpaired t-test). (D) Western blot analysis of expression of indicated proteins in HCT116 and CT26 cells following treatment with spautin-1 (10 uM) in the absence or presence of SP600125 (500 nM) or CC-401 (100 nM) for 24 hours. (E) Q-PCR analysis of Jun gene expression in indicated Jun knockdown cancer cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test). (F-I) Knockdown of Jun inhibited spautin-1-(10µM) induced Bad mRNA expression (F), cell death (G), Bad promoter activity (H), and CASP3 activity (I) in indicated cells (n = 3, *p < 0.05 versus control shRNA group, unpaired t-test).

    Techniques Used: Activation Assay, Expressing, Western Blot, shRNA, Activity Assay

    p bad ser136  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p bad ser136
    ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of <t>p-Bad</t> and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).
    P Bad Ser136, 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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    1) Product Images from "Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury"

    Article Title: Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0045763

    ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of p-Bad and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).
    Figure Legend Snippet: ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of p-Bad and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).

    Techniques Used: Western Blot

    Representative immunoblots and densitometric analysis showed that (A, B, C, D) levels of cleaved caspase 3, p-Akt Ser473, p-Akt Thr308, (E, F, G) p-Bad and p-FOXO1 in ipsilateral hippocampal samples from injured animals at post-injury day 1 or 3 were not significantly different from those in sham-injured animals (n = 6 mice/group at each time point, repeated measures two-way ANOVA).
    Figure Legend Snippet: Representative immunoblots and densitometric analysis showed that (A, B, C, D) levels of cleaved caspase 3, p-Akt Ser473, p-Akt Thr308, (E, F, G) p-Bad and p-FOXO1 in ipsilateral hippocampal samples from injured animals at post-injury day 1 or 3 were not significantly different from those in sham-injured animals (n = 6 mice/group at each time point, repeated measures two-way ANOVA).

    Techniques Used: Western Blot

    ( A, B, C, D, E, F ) Representative immunoblots and densitometric analysis in the cortex from sham-injured mice or mice subject to cortical impact injury, infused intracerebroventricular (icv) with saline (vehicle) or LY294002. Mice received either icv pretreatment of LY294002 followed by 20 mg/kg salidroside (SALD 20) after injury (S20Y group) or icv pretreatment of saline followed by SALD 20 after CCI (S20V group). LY294002 did not affect Akt, Bad, or FOXO1 phosphorylation in sham-operated mice, but it significantly abolished SALD 20-induced preservation of p-Akt Thr308 and p-FOXO1 levels in the ipsilateral hemisphere at 1 day post-injury. The levels of p-Akt Ser473 and p-Bad were similar between the S20V and S20LY groups. Values are presented as mean ± SEM; * P <0.05, ** P <0.01 versus sham + vehicle (ShamV), and & P <0.05 versus sham + LY294002 (ShamLY), and # P <0.05 versus S20V group (n = 6 mice/group, one-way ANOVA). ( G ) Representative cresyl violet-stained brain sections of S20V and S20LY mice at 28 days post-injury. Scale bar is 1 mm. ( H ) Quantification analysis showed that there was a significant decrease in the residual cerebral tissue ratio in the S20LY group compared with the S20S group. Values are presented as mean ± SEM; * P <0.05 versus S20V group (n = 6 mice/group, Student’s t -test).
    Figure Legend Snippet: ( A, B, C, D, E, F ) Representative immunoblots and densitometric analysis in the cortex from sham-injured mice or mice subject to cortical impact injury, infused intracerebroventricular (icv) with saline (vehicle) or LY294002. Mice received either icv pretreatment of LY294002 followed by 20 mg/kg salidroside (SALD 20) after injury (S20Y group) or icv pretreatment of saline followed by SALD 20 after CCI (S20V group). LY294002 did not affect Akt, Bad, or FOXO1 phosphorylation in sham-operated mice, but it significantly abolished SALD 20-induced preservation of p-Akt Thr308 and p-FOXO1 levels in the ipsilateral hemisphere at 1 day post-injury. The levels of p-Akt Ser473 and p-Bad were similar between the S20V and S20LY groups. Values are presented as mean ± SEM; * P <0.05, ** P <0.01 versus sham + vehicle (ShamV), and & P <0.05 versus sham + LY294002 (ShamLY), and # P <0.05 versus S20V group (n = 6 mice/group, one-way ANOVA). ( G ) Representative cresyl violet-stained brain sections of S20V and S20LY mice at 28 days post-injury. Scale bar is 1 mm. ( H ) Quantification analysis showed that there was a significant decrease in the residual cerebral tissue ratio in the S20LY group compared with the S20S group. Values are presented as mean ± SEM; * P <0.05 versus S20V group (n = 6 mice/group, Student’s t -test).

    Techniques Used: Western Blot, Preserving, Staining

    Antibodies used in immunofluorescence and western blot.
    Figure Legend Snippet: Antibodies used in immunofluorescence and western blot.

    Techniques Used: Immunofluorescence, Western Blot

    anti bad ps136  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti bad ps136
    Anti Bad Ps136, 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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    polyclonal rabbit anti human bcl 2 associated death promoter bad antibody  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc polyclonal rabbit anti human bcl 2 associated death promoter bad antibody
    (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, <t>Bcl-2</t> and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.
    Polyclonal Rabbit Anti Human Bcl 2 Associated Death Promoter Bad Antibody, 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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    1) Product Images from "c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate"

    Article Title: c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0030143

    (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, Bcl-2 and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.
    Figure Legend Snippet: (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, Bcl-2 and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.

    Techniques Used: Western Blot, Expressing

    ser136  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc ser136
    Ser136, 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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    anti bad  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti bad
    Anti Bad, 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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    ser112  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc ser112
    All antibodies used for detection in this study.
    Ser112, 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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    1) Product Images from "Immunohistochemistry of Colorectal Cancer Biomarker Phosphorylation Requires Controlled Tissue Fixation"

    Article Title: Immunohistochemistry of Colorectal Cancer Biomarker Phosphorylation Requires Controlled Tissue Fixation

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0113608

    All antibodies used for detection in this study.
    Figure Legend Snippet: All antibodies used for detection in this study.

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    Bad, 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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    Antibodies used in immunofluorescence and western blot.
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    ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of <t>p-Bad</t> and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).
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    Cell Signaling Technology Inc anti bad ps136
    ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of <t>p-Bad</t> and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).
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    (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, <t>Bcl-2</t> and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.
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    (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, <t>Bcl-2</t> and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.
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    All antibodies used for detection in this study.
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    Image Search Results


    Antibodies used in immunofluorescence and western blot.

    Journal: PLoS ONE

    Article Title: Post-Injury Treatment with 7,8-Dihydroxyflavone, a TrkB Receptor Agonist, Protects against Experimental Traumatic Brain Injury via PI3K/Akt Signaling

    doi: 10.1371/journal.pone.0113397

    Figure Lengend Snippet: Antibodies used in immunofluorescence and western blot.

    Article Snippet: Phospho-Bad Ser136 , Cell signaling , 4366 , Rabbit , Monoclonal , WB 1∶1000.

    Techniques: Immunofluorescence, Western Blot

    ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of p-Bad and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).

    Journal: PLoS ONE

    Article Title: Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury

    doi: 10.1371/journal.pone.0045763

    Figure Lengend Snippet: ( A, B, C ) Representative immunoblots and densitometric analysis showed a significant increase in p-Akt Ser473 level in the ipsilateral cortex of 20 mg/kg salidroside (SALD 20)-treated injured mice at day 1 compared with vehicle-treated injured mice. The level of p-Akt Thr308 was increased following SALD 20 treatment at day 3 compared with vehicle-treated injured mice. ( D, E, F ) Representative immunoblots and densitometric analysis showed that there were no differences in the levels of p-Bad and p-FOXO1 in the ipsilateral cortex between the SALD 20 and vehicle groups at day 1 or 3. ( G, H, I ) Representative immunoblots and densitometric analysis showed that the mitochondrial Bcl-2/Bax ratio significantly increased in SALD-20 treated injured mice but no difference was found in the total Bcl-2/Bax ratio. Values are presented as mean ± SEM; # P <0.05, ## P <0.01 versus sham controls, and * P <0.05 versus vehicle-treated injured mice (n = 6 mice/group at each time point, repeated measures two-way ANOVA for p-Akt Ser473, p-Akt Thr308, p-Bad, and p-FOXO1 levels; one-way ANOVA for Bcl-2/Bax ratio).

    Article Snippet: p-Bad (Ser136) , Cell signaling , 4366 , Rabbit , Monoclonal , WB 1∶1000.

    Techniques: Western Blot

    Representative immunoblots and densitometric analysis showed that (A, B, C, D) levels of cleaved caspase 3, p-Akt Ser473, p-Akt Thr308, (E, F, G) p-Bad and p-FOXO1 in ipsilateral hippocampal samples from injured animals at post-injury day 1 or 3 were not significantly different from those in sham-injured animals (n = 6 mice/group at each time point, repeated measures two-way ANOVA).

    Journal: PLoS ONE

    Article Title: Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury

    doi: 10.1371/journal.pone.0045763

    Figure Lengend Snippet: Representative immunoblots and densitometric analysis showed that (A, B, C, D) levels of cleaved caspase 3, p-Akt Ser473, p-Akt Thr308, (E, F, G) p-Bad and p-FOXO1 in ipsilateral hippocampal samples from injured animals at post-injury day 1 or 3 were not significantly different from those in sham-injured animals (n = 6 mice/group at each time point, repeated measures two-way ANOVA).

    Article Snippet: p-Bad (Ser136) , Cell signaling , 4366 , Rabbit , Monoclonal , WB 1∶1000.

    Techniques: Western Blot

    ( A, B, C, D, E, F ) Representative immunoblots and densitometric analysis in the cortex from sham-injured mice or mice subject to cortical impact injury, infused intracerebroventricular (icv) with saline (vehicle) or LY294002. Mice received either icv pretreatment of LY294002 followed by 20 mg/kg salidroside (SALD 20) after injury (S20Y group) or icv pretreatment of saline followed by SALD 20 after CCI (S20V group). LY294002 did not affect Akt, Bad, or FOXO1 phosphorylation in sham-operated mice, but it significantly abolished SALD 20-induced preservation of p-Akt Thr308 and p-FOXO1 levels in the ipsilateral hemisphere at 1 day post-injury. The levels of p-Akt Ser473 and p-Bad were similar between the S20V and S20LY groups. Values are presented as mean ± SEM; * P <0.05, ** P <0.01 versus sham + vehicle (ShamV), and & P <0.05 versus sham + LY294002 (ShamLY), and # P <0.05 versus S20V group (n = 6 mice/group, one-way ANOVA). ( G ) Representative cresyl violet-stained brain sections of S20V and S20LY mice at 28 days post-injury. Scale bar is 1 mm. ( H ) Quantification analysis showed that there was a significant decrease in the residual cerebral tissue ratio in the S20LY group compared with the S20S group. Values are presented as mean ± SEM; * P <0.05 versus S20V group (n = 6 mice/group, Student’s t -test).

    Journal: PLoS ONE

    Article Title: Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury

    doi: 10.1371/journal.pone.0045763

    Figure Lengend Snippet: ( A, B, C, D, E, F ) Representative immunoblots and densitometric analysis in the cortex from sham-injured mice or mice subject to cortical impact injury, infused intracerebroventricular (icv) with saline (vehicle) or LY294002. Mice received either icv pretreatment of LY294002 followed by 20 mg/kg salidroside (SALD 20) after injury (S20Y group) or icv pretreatment of saline followed by SALD 20 after CCI (S20V group). LY294002 did not affect Akt, Bad, or FOXO1 phosphorylation in sham-operated mice, but it significantly abolished SALD 20-induced preservation of p-Akt Thr308 and p-FOXO1 levels in the ipsilateral hemisphere at 1 day post-injury. The levels of p-Akt Ser473 and p-Bad were similar between the S20V and S20LY groups. Values are presented as mean ± SEM; * P <0.05, ** P <0.01 versus sham + vehicle (ShamV), and & P <0.05 versus sham + LY294002 (ShamLY), and # P <0.05 versus S20V group (n = 6 mice/group, one-way ANOVA). ( G ) Representative cresyl violet-stained brain sections of S20V and S20LY mice at 28 days post-injury. Scale bar is 1 mm. ( H ) Quantification analysis showed that there was a significant decrease in the residual cerebral tissue ratio in the S20LY group compared with the S20S group. Values are presented as mean ± SEM; * P <0.05 versus S20V group (n = 6 mice/group, Student’s t -test).

    Article Snippet: p-Bad (Ser136) , Cell signaling , 4366 , Rabbit , Monoclonal , WB 1∶1000.

    Techniques: Western Blot, Preserving, Staining

    Antibodies used in immunofluorescence and western blot.

    Journal: PLoS ONE

    Article Title: Salidroside Improves Behavioral and Histological Outcomes and Reduces Apoptosis via PI3K/Akt Signaling after Experimental Traumatic Brain Injury

    doi: 10.1371/journal.pone.0045763

    Figure Lengend Snippet: Antibodies used in immunofluorescence and western blot.

    Article Snippet: p-Bad (Ser136) , Cell signaling , 4366 , Rabbit , Monoclonal , WB 1∶1000.

    Techniques: Immunofluorescence, Western Blot

    (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, Bcl-2 and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.

    Journal: PLoS ONE

    Article Title: c-MET Protects Breast Cancer Cells from Apoptosis Induced by Sodium Butyrate

    doi: 10.1371/journal.pone.0030143

    Figure Lengend Snippet: (A) to (D) showed the effect of NaBu on breast cancer cell line MDA-MB-231(A and B) and MCF-7 (C and D). Majority of MDA-MB-231(B) and MCF-7(D) cancer cells were removed by the treatment of NaBu. Compared with 16% of viable MCF cells, the survival rate of MDA-MB-231 was significantly increased to 30%(E). Immunoblotting result of BAD, BAX, Bcl-2 and Cytochrome C expression indicated that MDA-MB-231 cells were resistant to the treatment of NaBu by neutralizing its apoptosis effect compared with MCF-7 cells (F). *P<0.05.

    Article Snippet: After blocking in a powdered nonfat milk solution (5% in PBS) with 0.05% Tween-20, the blot was incubated with a polyclonal rabbit anti- human Bcl-2-associated death promoter (BAD) antibody (Cell Signaling, Danvers, MA),a rabbit anti- human BAX antibody (Cell Signaling), a rabbit anti- human Bcl-2 antibody (Cell Signaling), a rabbit anti- human Cytochrome C antibody (Cell Signaling), a rabbit anti-human CD133 antibody (Cell Signaling) and a rabbit anti-human beta– actin antibody (Cell Signaling) at 1∶1000 dilutions in 5% blocking solution over night at 4°C.

    Techniques: Western Blot, Expressing

    All antibodies used for detection in this study.

    Journal: PLoS ONE

    Article Title: Immunohistochemistry of Colorectal Cancer Biomarker Phosphorylation Requires Controlled Tissue Fixation

    doi: 10.1371/journal.pone.0113608

    Figure Lengend Snippet: All antibodies used for detection in this study.

    Article Snippet: Phospho-BAD , 40A9 , 1∶40 , Ser112 , Cell Signalling Technologies, Danvers, MA , 5284.

    Techniques: