strong-cation exchange scx chromatography Search Results


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  • 99
    Thermo Fisher propac scx 10 strong cation exchange column
    Propac Scx 10 Strong Cation Exchange Column, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies strong cation exchange scx chromatography
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    Bonna-Agela Technologies strong cation exchange scx chromatography
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    Phenomenex strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Scx Chromatography, supplied by Phenomenex, used in various techniques. Bioz Stars score: 99/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Phenomenex strong cationic exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cationic Exchange Scx Chromatography, supplied by Phenomenex, used in various techniques. Bioz Stars score: 80/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PolyLC INC strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
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    Shimadzu Corporation strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Scx Chromatography, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 99/100, based on 140 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Phenomenex strong cation exchange chromatography scx column
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Chromatography Scx Column, supplied by Phenomenex, used in various techniques. Bioz Stars score: 98/100, based on 42 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PolyLC INC strong cation exchange chromatography scx column
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Chromatography Scx Column, supplied by PolyLC INC, used in various techniques. Bioz Stars score: 77/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PolyLC INC strong cation exchange scx chromatography toptip column
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Scx Chromatography Toptip Column, supplied by PolyLC INC, used in various techniques. Bioz Stars score: 86/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    GE Healthcare strong cation exchange chromatography scx
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Chromatography Scx, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 94/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    SCIEX strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Scx Chromatography, supplied by SCIEX, used in various techniques. Bioz Stars score: 86/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The Nest Group strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cation Exchange Scx Chromatography, supplied by The Nest Group, used in various techniques. Bioz Stars score: 97/100, based on 44 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher strong cation exchange chromatography scx
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
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    Biocad strong cation exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
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    Shimadzu Corporation strong cationic exchange scx chromatography
    Workflow for the <t>iTRAQ-based</t> quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the <t>SCX</t> fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.
    Strong Cationic Exchange Scx Chromatography, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 97/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Bio Basic Canada strong cation exchange scx chromatography
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
    Strong Cation Exchange Scx Chromatography, supplied by Bio Basic Canada, used in various techniques. Bioz Stars score: 84/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher strong cation exchange scx chromatography column
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    SCIEX strong cation exchange scx chromatography sample preparation
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    The Nest Group strong cation exchange scx liquid chromatography
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Agilent technologies strong cation exchange liquid chromatography scx
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Phenomenex lc ms ms analysis strong cation exchange scx chromatography
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
    Lc Ms Ms Analysis Strong Cation Exchange Scx Chromatography, supplied by Phenomenex, used in various techniques. Bioz Stars score: 82/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Thermo Fisher strong cation exchange scx chromatography itraq reagents
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Sangon Biotech strong cation exchange scx chromatography based fractionation scx chromatography based fractionation
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Phenomenex luna scx strong cation exchange high performance liquid chromatography column
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Agilent technologies strong cation exchange scx high performance liquid chromatography
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
    Strong Cation Exchange Scx High Performance Liquid Chromatography, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 78/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    PolyLC INC strong cation exchange high performance liquid chromatography scx hplc
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
    Strong Cation Exchange High Performance Liquid Chromatography Scx Hplc, supplied by PolyLC INC, used in various techniques. Bioz Stars score: 82/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Agilent technologies high performance liquid chromatography zorbax scx strong cation exchange column
    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
    High Performance Liquid Chromatography Zorbax Scx Strong Cation Exchange Column, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 77/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated <t>DG75</t> cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either <t>SCX/TiO</t> 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.
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    Image Search Results


    Workflow for the iTRAQ-based quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the SCX fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.

    Journal: PLoS ONE

    Article Title: iTRAQ-based quantitative proteomic analysis in vernalization-treated faba bean (Vicia faba L.)

    doi: 10.1371/journal.pone.0187436

    Figure Lengend Snippet: Workflow for the iTRAQ-based quantitative proteomic experiment. Protein samples were obtained from vernalization-treated (T) and non-treated (CK) faba bean seedlings. Three biological replicates of T and CK samples were digested and labeled with iTRAQ tags, followed by the SCX fractionation. The sufficient amounts of labeled peptides were used for LC-MS/MS analysis.

    Article Snippet: iTRAQ labeling and strong cation exchange (SCX) chromatography After trypsin digestion, peptides were desalted by the Strata X C18 SPE column (Phenomenex) and vacuum evaporation.

    Techniques: Labeling, Fractionation, Liquid Chromatography with Mass Spectroscopy, Mass Spectrometry

    ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated DG75 cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either SCX/TiO 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Elucidation of tonic and activated B-cell receptor signaling in Burkitt’s lymphoma provides insights into regulation of cell survival

    doi: 10.1073/pnas.1601053113

    Figure Lengend Snippet: ( A ) Schematic representation of a 3-plex SILAC approach for profiling phosphorylation dynamics in resting and BCR-stimulated DG75 cells. DG75 cells were cultured in SILAC medium as indicated and were left untreated, or were BCR-stimulated, for 2, 5, 10, or 20 min. Daudi cells were stimulated for 2 and 10 min. Lysates were mixed in a 1:1:1 ratio and digested with trypsin. Resulting phosphopeptides were enriched by either SCX/TiO 2 for details). ( B ) Schematic representation of a 2-plex SILAC approach for profiling phosphorylation changes upon inducible CD79a knockdown or upon SYK inhibition. DG75 cells were cultured in SILAC medium and treated as indicated. Lysates were processed as described in A . ( C ) DG75 and Daudi cells were loaded with the ratiometric Ca 2+ -chelator INDO-1-AM and subjected to BCR-induced Ca 2+ flux analysis by flow cytometry.

    Article Snippet: For samples of DG75 BCR stimulations, peptides were subsequently fractionated by strong cation exchange (SCX) chromatography (BioBasic SCX 50 × 2.1 mm; Thermo Fisher) on an FPLC system (SMART; Pharmacia) with a salt concentration gradient.

    Techniques: Cell Culture, Inhibition, Flow Cytometry, Cytometry