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phosphorylated c src  (Proteintech)


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    Structured Review

    Proteintech phosphorylated c src
    Phosphorylated C Src, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 2374 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phosphorylated+c+src/CEL+Antibody/pm41399133-75-5-12
    Average 96 stars, based on 2374 article reviews
    phosphorylated c src - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Western Blot:

    Article Title: Xanthone impairs platelet activation and thrombus formation.
    Article Snippet: .. The levels of total and phosphorylated c-Src (anti-Tyr416, Cell Signaling Technology; pan-c-Src, Proteintech), PLCγ2 (antiTyr1217 and pan-PLCγ2; Bioworld Technology), ERK1/2 (anti-Thr202/Tyr204 and pan-ERK1/2, Cell Signaling Technology), p38 (anti-Thr180/Tyr182, Cell Signaling Technology) and NF-ƙB p65 (antiSer536, Cell Signaling Technology; pan-NF-ƙB p65, Proteintech) were measured by western blot. ..



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    Image Search Results


    Serum-starved A549 cells were incubated (or not) with 1 µM AG1478 or 5 µM PP1 for 30 min. Then, the cells were treated for 30 min. with 100 ng/ml EGF or 1 U/ml GO, as indicated. EGFR was IPed from cell lysates, resolved by SDS-PAGE and IBed for total receptor, total tyrosine phosphorylation (p-EGFR) and specific Tyr-residue phosphorylation level (Y845, Y1068, Y1086, and Y1173). Protein aliquots of the cell lysates were also directly IBed for total and Y416 phosphorylated (active) c-Src (p-Src).

    Journal: PLoS ONE

    Article Title: EGF Receptor Exposed to Oxidative Stress Acquires Abnormal Phosphorylation and Aberrant Activated Conformation That Impairs Canonical Dimerization

    doi: 10.1371/journal.pone.0023240

    Figure Lengend Snippet: Serum-starved A549 cells were incubated (or not) with 1 µM AG1478 or 5 µM PP1 for 30 min. Then, the cells were treated for 30 min. with 100 ng/ml EGF or 1 U/ml GO, as indicated. EGFR was IPed from cell lysates, resolved by SDS-PAGE and IBed for total receptor, total tyrosine phosphorylation (p-EGFR) and specific Tyr-residue phosphorylation level (Y845, Y1068, Y1086, and Y1173). Protein aliquots of the cell lysates were also directly IBed for total and Y416 phosphorylated (active) c-Src (p-Src).

    Article Snippet: Primary Abs used in this study for the IBs were: α2232 (αEGFR, Cell Signaling, 1∶1000), αc-Src (Santa Cruz Biotech, 1∶2000), α tyrosine Y416 phosphorylated (p-) c-Src (Cell Signaling, 1∶2000), αp-Y20 (Santa Cruz Biotech, 1∶3000), αp-Y1173 EGFR (Santa Cruz Biotech, 1∶1000), αp-Y1086, αp-Y1068 and αp-Y845 EGFR (Cell Signaling, 1∶1000).

    Techniques: Incubation, SDS Page

    A549 cells were incubated (or not) with 5 µM PP1 for 45 min. and then treated (or not) for 15 min. with 100 ng/ml EGF or 30 min. 1 U/ml GO. A . EGFR was IPed from total cell lysates with the mAb 528 and IBed for Y416 phosphorylated c-Src (p-Src) and for total EGFR, as indicated. B . c-Src was IPed from total cell lysates and IBed for total c-Src and EGFR, as indicated.

    Journal: PLoS ONE

    Article Title: EGF Receptor Exposed to Oxidative Stress Acquires Abnormal Phosphorylation and Aberrant Activated Conformation That Impairs Canonical Dimerization

    doi: 10.1371/journal.pone.0023240

    Figure Lengend Snippet: A549 cells were incubated (or not) with 5 µM PP1 for 45 min. and then treated (or not) for 15 min. with 100 ng/ml EGF or 30 min. 1 U/ml GO. A . EGFR was IPed from total cell lysates with the mAb 528 and IBed for Y416 phosphorylated c-Src (p-Src) and for total EGFR, as indicated. B . c-Src was IPed from total cell lysates and IBed for total c-Src and EGFR, as indicated.

    Article Snippet: Primary Abs used in this study for the IBs were: α2232 (αEGFR, Cell Signaling, 1∶1000), αc-Src (Santa Cruz Biotech, 1∶2000), α tyrosine Y416 phosphorylated (p-) c-Src (Cell Signaling, 1∶2000), αp-Y20 (Santa Cruz Biotech, 1∶3000), αp-Y1173 EGFR (Santa Cruz Biotech, 1∶1000), αp-Y1086, αp-Y1068 and αp-Y845 EGFR (Cell Signaling, 1∶1000).

    Techniques: Incubation

    A . Serum-starved A549 cells were treated, or not, with 100 ng/ml EGF for 15 min. or 2% (w/v) MβCD for 1 h and cell lysates were IBed for total and Tyr-phosphorylated EGFR. B and C . Cells were treated with EGF as in A or with 1 U/ml GO for 30 min. in the absence or presence of 2 mM MβCD-cholesterol complex (CC), prepared as described in “ ”. Cell lysates were separated by SDS-PAGE and IBed for total and Tyr-phosphorylated EGFR ( B ) or total and Y416 phosphorylated Src ( C ).

    Journal: PLoS ONE

    Article Title: EGF Receptor Exposed to Oxidative Stress Acquires Abnormal Phosphorylation and Aberrant Activated Conformation That Impairs Canonical Dimerization

    doi: 10.1371/journal.pone.0023240

    Figure Lengend Snippet: A . Serum-starved A549 cells were treated, or not, with 100 ng/ml EGF for 15 min. or 2% (w/v) MβCD for 1 h and cell lysates were IBed for total and Tyr-phosphorylated EGFR. B and C . Cells were treated with EGF as in A or with 1 U/ml GO for 30 min. in the absence or presence of 2 mM MβCD-cholesterol complex (CC), prepared as described in “ ”. Cell lysates were separated by SDS-PAGE and IBed for total and Tyr-phosphorylated EGFR ( B ) or total and Y416 phosphorylated Src ( C ).

    Article Snippet: Primary Abs used in this study for the IBs were: α2232 (αEGFR, Cell Signaling, 1∶1000), αc-Src (Santa Cruz Biotech, 1∶2000), α tyrosine Y416 phosphorylated (p-) c-Src (Cell Signaling, 1∶2000), αp-Y20 (Santa Cruz Biotech, 1∶3000), αp-Y1173 EGFR (Santa Cruz Biotech, 1∶1000), αp-Y1086, αp-Y1068 and αp-Y845 EGFR (Cell Signaling, 1∶1000).

    Techniques: SDS Page

    A549 cells were seeded on cover-glasses, serum starved for 1 h and treated (or not) with 1 U/ml GO as indicated. After treatments, ceramide, EGFR phosphorylated on Y1173 and Y416 phosphorylated c-Src were localized in situ by IF as indicated in “ ”; nuclei were stained by DAPI.

    Journal: PLoS ONE

    Article Title: EGF Receptor Exposed to Oxidative Stress Acquires Abnormal Phosphorylation and Aberrant Activated Conformation That Impairs Canonical Dimerization

    doi: 10.1371/journal.pone.0023240

    Figure Lengend Snippet: A549 cells were seeded on cover-glasses, serum starved for 1 h and treated (or not) with 1 U/ml GO as indicated. After treatments, ceramide, EGFR phosphorylated on Y1173 and Y416 phosphorylated c-Src were localized in situ by IF as indicated in “ ”; nuclei were stained by DAPI.

    Article Snippet: Primary Abs used in this study for the IBs were: α2232 (αEGFR, Cell Signaling, 1∶1000), αc-Src (Santa Cruz Biotech, 1∶2000), α tyrosine Y416 phosphorylated (p-) c-Src (Cell Signaling, 1∶2000), αp-Y20 (Santa Cruz Biotech, 1∶3000), αp-Y1173 EGFR (Santa Cruz Biotech, 1∶1000), αp-Y1086, αp-Y1068 and αp-Y845 EGFR (Cell Signaling, 1∶1000).

    Techniques: In Situ, Staining

    A549 cells were seeded on cover-glasses, serum starved for 1 h and treated (or not) with 1 U/ml GO as indicated. After treatments, ceramide ( A and B ), EGFR phosphorylated on Y1173 ( A ) and Y416 phosphorylated c-Src ( B ) were localized in situ by IF as indicated in “ ”; nuclei were stained by DAPI. White arrows indicate regions where p-Y1173 EGFR and ceramide ( A ) or p-Y416 c-Src (p-Src) and ceramide ( B ) co-localized under ox-stress (GO). Z-stack sections of cells have been discriminated by confocal microscopy: the panels show the merge of all of the Z-stack sections.

    Journal: PLoS ONE

    Article Title: EGF Receptor Exposed to Oxidative Stress Acquires Abnormal Phosphorylation and Aberrant Activated Conformation That Impairs Canonical Dimerization

    doi: 10.1371/journal.pone.0023240

    Figure Lengend Snippet: A549 cells were seeded on cover-glasses, serum starved for 1 h and treated (or not) with 1 U/ml GO as indicated. After treatments, ceramide ( A and B ), EGFR phosphorylated on Y1173 ( A ) and Y416 phosphorylated c-Src ( B ) were localized in situ by IF as indicated in “ ”; nuclei were stained by DAPI. White arrows indicate regions where p-Y1173 EGFR and ceramide ( A ) or p-Y416 c-Src (p-Src) and ceramide ( B ) co-localized under ox-stress (GO). Z-stack sections of cells have been discriminated by confocal microscopy: the panels show the merge of all of the Z-stack sections.

    Article Snippet: Primary Abs used in this study for the IBs were: α2232 (αEGFR, Cell Signaling, 1∶1000), αc-Src (Santa Cruz Biotech, 1∶2000), α tyrosine Y416 phosphorylated (p-) c-Src (Cell Signaling, 1∶2000), αp-Y20 (Santa Cruz Biotech, 1∶3000), αp-Y1173 EGFR (Santa Cruz Biotech, 1∶1000), αp-Y1086, αp-Y1068 and αp-Y845 EGFR (Cell Signaling, 1∶1000).

    Techniques: In Situ, Staining, Confocal Microscopy