p 4e bp  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p 4e bp
    P 4e Bp, 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
    https://www.bioz.com/result/p 4e bp/product/Cell Signaling Technology Inc
    Average 96 stars, based on 1 article reviews
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    anti phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho 4e bp1
    KEY RESOURCES TABLE
    Anti Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "A multiplexed in vivo approach to identify driver genes in small cell lung cancer"

    Article Title: A multiplexed in vivo approach to identify driver genes in small cell lung cancer

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.111990

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Plasmid Preparation, Recombinant, Modification, Labeling, Amplification, Staining, Protease Inhibitor, Bicinchoninic Acid Protein Assay, Western Blot, DNA Extraction, Purification, Sequencing, Generated, Software

    rabbit anti phospho 4e bp1 ser65 polyclonal  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti phospho 4e bp1 ser65 polyclonal
    KEY RESOURCES TABLE
    Rabbit Anti Phospho 4e Bp1 Ser65 Polyclonal, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti phospho 4e bp1 ser65 polyclonal/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti phospho 4e bp1 ser65 polyclonal - by Bioz Stars, 2023-03
    86/100 stars

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    1) Product Images from "A multiplexed in vivo approach to identify driver genes in small cell lung cancer"

    Article Title: A multiplexed in vivo approach to identify driver genes in small cell lung cancer

    Journal: Cell reports

    doi: 10.1016/j.celrep.2023.111990

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Plasmid Preparation, Recombinant, Modification, Labeling, Amplification, Staining, Protease Inhibitor, Bicinchoninic Acid Protein Assay, Western Blot, DNA Extraction, Purification, Sequencing, Generated, Software

    phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho 4e bp1
    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), <t>S6RP,</t> <t>p–4E-BP1</t> <t>(Thr37/46),</t> and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.
    Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho 4e bp1/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    phospho 4e bp1 - by Bioz Stars, 2023-03
    86/100 stars

    Images

    1) Product Images from "TFEB-mediated lysosomal exocytosis alleviates high-fat diet–induced lipotoxicity in the kidney"

    Article Title: TFEB-mediated lysosomal exocytosis alleviates high-fat diet–induced lipotoxicity in the kidney

    Journal: JCI Insight

    doi: 10.1172/jci.insight.162498

    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), S6RP, p–4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.
    Figure Legend Snippet: ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), S6RP, p–4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.

    Techniques Used: Western Blot, Cell Culture, Immunofluorescence, Transfection, Translocation Assay

    anti phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho 4e bp1
    ( A ) Morphological appearance of salispheres at different time points; day 1 (D1), day 2 (D2), day 3 (D3), and day 4 (D4) of culture (scale bar = 20 µm). ( B ) Immunoblotting of mTOR substrates; p-S6 rp <t>and</t> <t>p-4e-bp1</t> at days 1, 2, 3, and 4 of culture showed active mTOR. ( C ) Densitometric analysis reveals a gradual but insignificant increase in the phosphorylation of S6 rp ( p = 0.2391). ( D ) A significant increase in the phosphorylation of 4e-bp1 was detected on days 3 and 4 compared to day 1 of culture (* p < 0.05). Data are expressed as mean ± S.E.M ( n = 6) in arbitrary units (AUs).
    Anti Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti phospho 4e bp1/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    anti phospho 4e bp1 - by Bioz Stars, 2023-03
    86/100 stars

    Images

    1) Product Images from "The Role of mTOR and Injury in Developing Salispheres"

    Article Title: The Role of mTOR and Injury in Developing Salispheres

    Journal: Biomedicines

    doi: 10.3390/biomedicines11020604

    ( A ) Morphological appearance of salispheres at different time points; day 1 (D1), day 2 (D2), day 3 (D3), and day 4 (D4) of culture (scale bar = 20 µm). ( B ) Immunoblotting of mTOR substrates; p-S6 rp and p-4e-bp1 at days 1, 2, 3, and 4 of culture showed active mTOR. ( C ) Densitometric analysis reveals a gradual but insignificant increase in the phosphorylation of S6 rp ( p = 0.2391). ( D ) A significant increase in the phosphorylation of 4e-bp1 was detected on days 3 and 4 compared to day 1 of culture (* p < 0.05). Data are expressed as mean ± S.E.M ( n = 6) in arbitrary units (AUs).
    Figure Legend Snippet: ( A ) Morphological appearance of salispheres at different time points; day 1 (D1), day 2 (D2), day 3 (D3), and day 4 (D4) of culture (scale bar = 20 µm). ( B ) Immunoblotting of mTOR substrates; p-S6 rp and p-4e-bp1 at days 1, 2, 3, and 4 of culture showed active mTOR. ( C ) Densitometric analysis reveals a gradual but insignificant increase in the phosphorylation of S6 rp ( p = 0.2391). ( D ) A significant increase in the phosphorylation of 4e-bp1 was detected on days 3 and 4 compared to day 1 of culture (* p < 0.05). Data are expressed as mean ± S.E.M ( n = 6) in arbitrary units (AUs).

    Techniques Used: Western Blot

    ( A ) Immunoblotting of p-S6 rp and p-4e-bp1 in untreated (control) and salispheres treated with rapamycin, LiCl, and the combination of rapamycin and LiCl (rapamycin + LiCl). ( B ). Rapamycin alone or combined with LiCl completely abolished the expression of p-S6 rp (**** p < 0.0001), but LiCl only did not affect the expression of p-S6 rp ( p = 0.8898). ( C ) A considerable reduction in the phosphorylation of 4e-bp1 was observed in salispheres treated with rapamycin alone and co-treated with rapamycin and LiCl (* p < 0.05). In contrast, a significant increase in the phosphorylation of 4e-bp1 was detected in LiCl-treated salispheres (*** p = 0.0006). The bar represents the mean ± S.E.M ( n = 6).
    Figure Legend Snippet: ( A ) Immunoblotting of p-S6 rp and p-4e-bp1 in untreated (control) and salispheres treated with rapamycin, LiCl, and the combination of rapamycin and LiCl (rapamycin + LiCl). ( B ). Rapamycin alone or combined with LiCl completely abolished the expression of p-S6 rp (**** p < 0.0001), but LiCl only did not affect the expression of p-S6 rp ( p = 0.8898). ( C ) A considerable reduction in the phosphorylation of 4e-bp1 was observed in salispheres treated with rapamycin alone and co-treated with rapamycin and LiCl (* p < 0.05). In contrast, a significant increase in the phosphorylation of 4e-bp1 was detected in LiCl-treated salispheres (*** p = 0.0006). The bar represents the mean ± S.E.M ( n = 6).

    Techniques Used: Western Blot, Expressing

    ( A ) Immunoblotting of p-S6 rp of growing salispheres from an unoperated gland (control) and from the ligated gland on day 8 of culture. ( B ) The phosphorylation of p-S6 rp in salispheres from ligated glands appeared comparable ( p = 0.3570) to that in salispheres from unoperated glands. ( C ) Immunoblotting of p-4e-bp1 of growing salispheres from an unoperated gland (control) and from the ligated gland. ( D ) The phosphorylation of 4e-bp1 was significantly inhibited in grown salispheres from ligated glands (** p < 0.005). Data are expressed as mean ± S.E.M ( n = 4).
    Figure Legend Snippet: ( A ) Immunoblotting of p-S6 rp of growing salispheres from an unoperated gland (control) and from the ligated gland on day 8 of culture. ( B ) The phosphorylation of p-S6 rp in salispheres from ligated glands appeared comparable ( p = 0.3570) to that in salispheres from unoperated glands. ( C ) Immunoblotting of p-4e-bp1 of growing salispheres from an unoperated gland (control) and from the ligated gland. ( D ) The phosphorylation of 4e-bp1 was significantly inhibited in grown salispheres from ligated glands (** p < 0.005). Data are expressed as mean ± S.E.M ( n = 4).

    Techniques Used: Western Blot

    phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho 4e bp1
    Expression of glucocorticoid-responsive genes under chronic stress conditions. ( A ) Expression levels of genes associated with protein degradation were significantly higher in the WRS group, although myostatin, an inhibitor of muscle proliferation, and myogenin, a marker of muscle differentiation, remained unaffected. ( B , C ) Phosphorylation of S6 <t>and</t> <t>4E-BP1,</t> both downstream regulators of mTOR-mediated signal transduction, was significantly lower in mice in the WRS group than in those in the control group. **: p < 0.01, *: p < 0.05. Original picture for Western blot analysis in all mice is shown in .
    Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho 4e bp1/product/Cell Signaling Technology Inc
    Average 86 stars, based on 1 article reviews
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    phospho 4e bp1 - by Bioz Stars, 2023-03
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    Images

    1) Product Images from "Chronic Stress Induces Type 2b Skeletal Muscle Atrophy via the Inhibition of mTORC1 Signaling in Mice"

    Article Title: Chronic Stress Induces Type 2b Skeletal Muscle Atrophy via the Inhibition of mTORC1 Signaling in Mice

    Journal: Medical Sciences

    doi: 10.3390/medsci11010019

    Expression of glucocorticoid-responsive genes under chronic stress conditions. ( A ) Expression levels of genes associated with protein degradation were significantly higher in the WRS group, although myostatin, an inhibitor of muscle proliferation, and myogenin, a marker of muscle differentiation, remained unaffected. ( B , C ) Phosphorylation of S6 and 4E-BP1, both downstream regulators of mTOR-mediated signal transduction, was significantly lower in mice in the WRS group than in those in the control group. **: p < 0.01, *: p < 0.05. Original picture for Western blot analysis in all mice is shown in .
    Figure Legend Snippet: Expression of glucocorticoid-responsive genes under chronic stress conditions. ( A ) Expression levels of genes associated with protein degradation were significantly higher in the WRS group, although myostatin, an inhibitor of muscle proliferation, and myogenin, a marker of muscle differentiation, remained unaffected. ( B , C ) Phosphorylation of S6 and 4E-BP1, both downstream regulators of mTOR-mediated signal transduction, was significantly lower in mice in the WRS group than in those in the control group. **: p < 0.01, *: p < 0.05. Original picture for Western blot analysis in all mice is shown in .

    Techniques Used: Expressing, Marker, Transduction, Western Blot

    phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc phospho 4e bp1
    Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti phospho 4e bp1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho 4e bp1
    Anti Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti phospho 4e bp1/product/Cell Signaling Technology Inc
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    anti phospho 4e bp1 thr37 46  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phospho 4e bp1 thr37 46
    Anti Phospho 4e Bp1 Thr37 46, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti phospho 4e bp1 thr37 46/product/Cell Signaling Technology Inc
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    p 4e bp  (Cell Signaling Technology Inc)


    Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
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    Cell Signaling Technology Inc p 4e bp
    P 4e Bp, 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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    anti e4 bp1 p thr37 46  (Cell Signaling Technology Inc)


    Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
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    Cell Signaling Technology Inc anti e4 bp1 p thr37 46
    Anti E4 Bp1 P Thr37 46, 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 4e bp
    P 4e Bp, 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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    KEY RESOURCES TABLE
    Anti Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    rabbit anti phospho 4e bp1 ser65 polyclonal  (Cell Signaling Technology Inc)
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    phospho 4e bp1  (Cell Signaling Technology Inc)
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    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), <t>S6RP,</t> <t>p–4E-BP1</t> <t>(Thr37/46),</t> and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.
    Phospho 4e Bp1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho 4e bp1/product/Cell Signaling Technology Inc
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    anti phospho 4e bp1 thr37 46  (Cell Signaling Technology Inc)
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    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), <t>S6RP,</t> <t>p–4E-BP1</t> <t>(Thr37/46),</t> and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.
    Anti Phospho 4e Bp1 Thr37 46, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), <t>S6RP,</t> <t>p–4E-BP1</t> <t>(Thr37/46),</t> and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.
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    Image Search Results


    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: A multiplexed in vivo approach to identify driver genes in small cell lung cancer

    doi: 10.1016/j.celrep.2023.111990

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: The following antibodies were used: anti-HSP90 (CST 4877, 1:4,000), anti-TSC1 (D43E2, CST 6935, 1:200), anti-TSC2 (D93F12, CST 4308), anti-S6 (CST 2217, 1:200), anti-phospho-S6 (Ser235/236, CST 2211, 1:200), anti-GFP (D5.1, CST 2956, 1:200), anti-p-mTOR (D9C2, Ser2448, CST 55365, 1:200), anti-mTOR (CST 2972, 1:200), anti-phospho-4E-BP1 (Ser65, CST 9451, 1:200), and anti-4E-BP1 (53H11, CST 9644, 1:200).

    Techniques: Plasmid Preparation, Recombinant, Modification, Labeling, Amplification, Staining, Protease Inhibitor, Bicinchoninic Acid Protein Assay, Western Blot, DNA Extraction, Purification, Sequencing, Generated, Software

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: A multiplexed in vivo approach to identify driver genes in small cell lung cancer

    doi: 10.1016/j.celrep.2023.111990

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit anti-phospho-4E-BP1 (Ser65) Polyclonal , Cell Signaling Technology , Cat#9451; RRID:AB_330947.

    Techniques: Plasmid Preparation, Recombinant, Modification, Labeling, Amplification, Staining, Protease Inhibitor, Bicinchoninic Acid Protein Assay, Western Blot, DNA Extraction, Purification, Sequencing, Generated, Software

    ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), S6RP, p–4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.

    Journal: JCI Insight

    Article Title: TFEB-mediated lysosomal exocytosis alleviates high-fat diet–induced lipotoxicity in the kidney

    doi: 10.1172/jci.insight.162498

    Figure Lengend Snippet: ( A ) Representative Western blot images of phosphorylated (p-) TFEB S211, total TFEB, p-S6RP (Ser235/236), S6RP, p–4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs after Torin 1, BSA, or PA treatment for 6 hours ( n = 3). ( B ) Representative Western blot images of p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs subjected to BSA or PA treatment for the indicated periods ( n = 3). The values are normalized by the value at time 0. ( C ) Representative immunofluorescence images of TFEB (green) in cultured PTECs transfected with a constitutively active form of HA-tagged RagC for 48 hours, including treatment with Torin 1, BSA, or PA for the last 6 hours ( n = 3). Cells were immunostained for HA (red) and counterstained with DAPI (blue). The percentage of PTECs exhibiting TFEB nuclear translocation was determined in wild-type PTECs (RagC − ) and PTECs transfected with HA-tagged RagC (RagC + ). ( D ) Representative Western blot images of TFEB, p-S6RP (Ser235/236), S6RP, p-4E-BP1 (Thr37/46), and 4E-BP1 in cultured PTECs either starved of amino acids for 60 minutes or starved for 60 minutes and then restimulated with amino acids for 30 minutes after BSA or PA treatment for 6 hours ( n = 3). Bars: 10 μm ( C ). Data are provided as means ± SEM. Statistically significant differences: * P < 0.05 versus RagC − PTECs with the same treatment; # P < 0.05 versus BSA-treated PTECs ( A and B , 2-tailed Student’s t test; C , 1-way ANOVA followed by the Tukey-Kramer test). S6RP, S6 ribosomal protein.

    Article Snippet: We used the following antibodies: LRP2/MEGALIN (gifted by T. Michigami, Department of Bone and Mineral Research, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan), TFEB (Bethyl, A303-673A, for mouse samples; Cell Signaling Technology, 37785, for human samples), phospho-TFEB (Ser211; Cell Signaling Technology, 37681), Lamin A/C (Cell Signaling Technology, 2032), GAPDH (GeneTex, GTX100118), S6RP (Cell Signaling Technology, 2217), phospho-S6RP (Ser235/236; Cell Signaling Technology, 2211), 4E-BP1 (Cell Signaling Technology, 9644), phospho-4E-BP1 (Thr37/46; Cell Signaling Technology, 2855), MTOR (Cell Signaling Technology, 2983), ACTB (MilliporeSigma, A5316), HA (MilliporeSigma, 11867423001), FLCN (Cell Signaling Technology, 3697), GABARAP (MBL, PM037), LAMP1 (BD Biosciences, 553792 for mouse samples; BD Biosciences, 555798 for human samples), CTSD (Santa Cruz Biotechnology, sc-6486), TMEM55B (Proteintech, 23992-1-AP), MAP1LC3B (Cell Signaling Technology, 2775), COL1A1 (Abcam, ab34710), F4/80 (Bio-Rad, MCA497), GALECTIN-3 (Santa Cruz Biotechnology, sc-23938), SQSTM1/p62 (PROGEN, GP62-C), biotinylated secondary antibodies (Vector Laboratories, BA-1000, BA-2001, BA-4000, and BA-7000), horseradish peroxidase–conjugated secondary antibodies (DAKO, P0447, P0448, P0449, and P0450), and Alexa Fluor–conjugated secondary antibodies (Thermo Fisher Scientific, A21206, A21208, A21434, and A31572).

    Techniques: Western Blot, Cell Culture, Immunofluorescence, Transfection, Translocation Assay