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tyrosine phosphorylation proarray pst228 antibody  (Full Moon BioSystems)

 
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    Full Moon BioSystems tyrosine phosphorylation proarray pst228 antibody
    Tyrosine Phosphorylation Proarray Pst228 Antibody, supplied by Full Moon BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tyrosine+phosphorylation+proarray/tyrosine+phosphorylation+proarray/pm38572108-78-10-23
    Average 90 stars, based on 1 article reviews
    tyrosine phosphorylation proarray pst228 antibody - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Phospho-proteomics:

    Article Title: Met/HGFR triggers detrimental reactive microglia in TBI.
    Article Snippet: .. Tyrosine kinase array processing Tyrosine phosphorylation proarray (Full moon Biosystems, Sunnyvale, CA) were used to determine the phosphorylation of 228 phosphorylation targets. ..

    Article Title: Legionella pneumophila effector Lem4 is a membrane-associated protein tyrosine phosphatase
    Article Snippet: .. Phospho-specific protein microarray analysis Tyrosine Phosphorylation ProArray was purchased from Full Moon Biosystems (Sunnyvale, CA, USA). ..

    Article Title: Activation of RAW264.7 mouse macrophage cells in vitro through treatment with recombinant ricin toxin-binding subunit B: involvement of protein tyrosine, NF-κB and JAK-STAT kinase signaling pathways.
    Article Snippet: Phosphoprotein arrays were obtained from Full Moon Biosystems (Sunnyvale, CA, USA) and 228 site-specific tyrosine phosphorylation profiles were detected with 6 replicates each. .. The protein samples were biotinylated using Tyrosine Phosphorylation ProArray (Full Moon BioSystems), and the biotin-labeled protein samples were conjugated to antibodies using the Array Assay Kit (Full Moon BioSystems). ..

    Article Title: CBL mutation-related patterns of phosphorylation and sensitivity to tyrosine kinase inhibitors.
    Article Snippet: .. Phospho-specific protein microarray analysis For detection of 228 site-specific tyrosine phosphorylation profiles with six replicates each, 100 ug of cell lysate was labeled with biotin and hybridized on Tyrosine Phosphorylation ProArray (Full Moon BioSystems, Sunnyvale, CA, USA) using Antibody Array Assay Kit (Full Moon BioSystems). ..

    Article Title: Regulation of autoimmune arthritis by the SHP-1 tyrosine phosphatase
    Article Snippet: .. To determine which proteins were tyrosine-phosphorylated differentially in the CD4 + T cells of WT versus Shp1 -Tg mice, Tyrosine Phosphorylation ProArray was performed by the Full Moon Biosystems (Sunnyvale, CA). ..

    Article Title: Mesenchyme-specific deletion of Tgf-β1 in the embryonic lung disrupts branching morphogenesis and induces lung hypoplasia
    Article Snippet: .. Tyrosine Phosphorylation ProArray Kit Tyrosine Phosphorylation ProArray was bought from Full Moon Biosystems (Sunnyvale, CA, USA) (#PST228). ..

    Article Title: Legionella pneumophila effector Lem4 is a membrane-associated protein tyrosine phosphatase
    Article Snippet: .. Effect of Lem4 on tyrosine phosphorylation of signal proteins in HEK293T cell line, as detected by Tyrosine Phosphorylation ProArray (Full Moon BioSystems). ..

    Article Title: Legionella pneumophila effector Lem4 is a membrane-associated protein tyrosine phosphatase
    Article Snippet: .. KEGG pathway analysis revealed that three pathways were affected in the Lem4-overexpressing cell line: JAK–STAT-signaling pathway (EGFR, JAK1, JAK2, PDGF-Rβ, SHP-1, SHP-2, STAT1, and TYK2); focal adhesion pathway (CRK, β-catenin, EGFR, PDGF-Rβ, JNK1/2/3, FAK, SHC1, and vinculin); and regulation of actin cytoskeleton (CRK, EGFR, PDGF-R, focal adhesion kinase, caveolin-1, and vinculin). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window Figure 8. caption a7 Effect of Lem4 on tyrosine phosphorylation of signal proteins in HEK293T cell line, as detected by tyrosine phosphorylation ProArray (Full Moon BioSystems). ..

    Microarray:

    Article Title: Legionella pneumophila effector Lem4 is a membrane-associated protein tyrosine phosphatase
    Article Snippet: .. Phospho-specific protein microarray analysis Tyrosine Phosphorylation ProArray was purchased from Full Moon Biosystems (Sunnyvale, CA, USA). ..

    Article Title: CBL mutation-related patterns of phosphorylation and sensitivity to tyrosine kinase inhibitors.
    Article Snippet: .. Phospho-specific protein microarray analysis For detection of 228 site-specific tyrosine phosphorylation profiles with six replicates each, 100 ug of cell lysate was labeled with biotin and hybridized on Tyrosine Phosphorylation ProArray (Full Moon BioSystems, Sunnyvale, CA, USA) using Antibody Array Assay Kit (Full Moon BioSystems). ..

    Labeling:

    Article Title: CBL mutation-related patterns of phosphorylation and sensitivity to tyrosine kinase inhibitors.
    Article Snippet: .. Phospho-specific protein microarray analysis For detection of 228 site-specific tyrosine phosphorylation profiles with six replicates each, 100 ug of cell lysate was labeled with biotin and hybridized on Tyrosine Phosphorylation ProArray (Full Moon BioSystems, Sunnyvale, CA, USA) using Antibody Array Assay Kit (Full Moon BioSystems). ..

    Ab Array:

    Article Title: CBL mutation-related patterns of phosphorylation and sensitivity to tyrosine kinase inhibitors.
    Article Snippet: .. Phospho-specific protein microarray analysis For detection of 228 site-specific tyrosine phosphorylation profiles with six replicates each, 100 ug of cell lysate was labeled with biotin and hybridized on Tyrosine Phosphorylation ProArray (Full Moon BioSystems, Sunnyvale, CA, USA) using Antibody Array Assay Kit (Full Moon BioSystems). ..



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    tyrosine phosphorylation proarray pst228 antibody  (Full Moon BioSystems)
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    Tyrosine Phosphorylation Proarray Pst228 Antibody, supplied by Full Moon BioSystems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tyrosine+phosphorylation+proarray/tyrosine+phosphorylation+proarray/pm38572108-78-10-23
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    tyrosine phosphorylation proarray pst228  (Full Moon BioSystems)
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    Increased levels of phospho-FGFR1 in cardiomyocytes of diabetic mice. C57BL/6 mice were made diabetic by STZ. Heart tissues were harvested after 20 weeks of disease duration from diabetic (STZ) and non-diabetic control (Ctrl) mice. (A, B) Representative site-specific tyrosine kinase <t>phosphorylation</t> <t>PST228</t> <t>ProArray</t> showing phosphorylated proteins (A). Magnified images and signal-to-noise ratio (SNR) of FGFR1 (Tyr766) in STZ (red box) and Ctrl (yellow box) are shown in panel (B). (C) Relative abundance of FGFR1 protein in STZ and Ctrl heart tissues from AVK276 Kinase Array were shown. (D) Representative blots showing the levels of p-FGFR1 (Tyr-766) and FGFR1 in heart tissue. GAPDH was used as a loading control. (E) Immunofluorescence staining of mouse heart tissues for p-FGFR1 (red), FGFR1 (red), and α -actinin (green). Sections were counterstained with DAPI (blue). Arrows showing p-FGFR1-positive cells (Scale bar = 50 μm). (F) Levels of p-FGFR1 (Tyr-766) and FGFR1 in primary adult mouse cardiomyocytes and cardiac fibroblasts. Cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control. (G) Levels of p-FGFR1 (Tyr-766) and FGFR1 in rat primary cardiomyocytes. Isolated cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control.
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    tyrosine phosphorylation proarray  (Full Moon BioSystems)
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    Increased levels of phospho-FGFR1 in cardiomyocytes of diabetic mice. C57BL/6 mice were made diabetic by STZ. Heart tissues were harvested after 20 weeks of disease duration from diabetic (STZ) and non-diabetic control (Ctrl) mice. (A, B) Representative site-specific tyrosine kinase <t>phosphorylation</t> <t>PST228</t> <t>ProArray</t> showing phosphorylated proteins (A). Magnified images and signal-to-noise ratio (SNR) of FGFR1 (Tyr766) in STZ (red box) and Ctrl (yellow box) are shown in panel (B). (C) Relative abundance of FGFR1 protein in STZ and Ctrl heart tissues from AVK276 Kinase Array were shown. (D) Representative blots showing the levels of p-FGFR1 (Tyr-766) and FGFR1 in heart tissue. GAPDH was used as a loading control. (E) Immunofluorescence staining of mouse heart tissues for p-FGFR1 (red), FGFR1 (red), and α -actinin (green). Sections were counterstained with DAPI (blue). Arrows showing p-FGFR1-positive cells (Scale bar = 50 μm). (F) Levels of p-FGFR1 (Tyr-766) and FGFR1 in primary adult mouse cardiomyocytes and cardiac fibroblasts. Cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control. (G) Levels of p-FGFR1 (Tyr-766) and FGFR1 in rat primary cardiomyocytes. Isolated cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control.
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    tyrosine phosphorylation proarray #pst228  (Full Moon BioSystems)
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    Increased levels of phospho-FGFR1 in cardiomyocytes of diabetic mice. C57BL/6 mice were made diabetic by STZ. Heart tissues were harvested after 20 weeks of disease duration from diabetic (STZ) and non-diabetic control (Ctrl) mice. (A, B) Representative site-specific tyrosine kinase <t>phosphorylation</t> <t>PST228</t> <t>ProArray</t> showing phosphorylated proteins (A). Magnified images and signal-to-noise ratio (SNR) of FGFR1 (Tyr766) in STZ (red box) and Ctrl (yellow box) are shown in panel (B). (C) Relative abundance of FGFR1 protein in STZ and Ctrl heart tissues from AVK276 Kinase Array were shown. (D) Representative blots showing the levels of p-FGFR1 (Tyr-766) and FGFR1 in heart tissue. GAPDH was used as a loading control. (E) Immunofluorescence staining of mouse heart tissues for p-FGFR1 (red), FGFR1 (red), and α -actinin (green). Sections were counterstained with DAPI (blue). Arrows showing p-FGFR1-positive cells (Scale bar = 50 μm). (F) Levels of p-FGFR1 (Tyr-766) and FGFR1 in primary adult mouse cardiomyocytes and cardiac fibroblasts. Cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control. (G) Levels of p-FGFR1 (Tyr-766) and FGFR1 in rat primary cardiomyocytes. Isolated cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control.
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    phospho-specific protein microarray analysis tyrosine phosphorylation proarray  (Full Moon BioSystems)
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    Full Moon BioSystems phospho-specific protein microarray analysis tyrosine phosphorylation proarray
    Effect of Lem4 on tyrosine <t>phosphorylation</t> of signal proteins in HEK293T cell line, as detected by tyrosine phosphorylation <t>ProArray</t> (Full Moon BioSystems). Phosphorylation levels were increased by at least 30% at 30 sites and decreased by at least 30% at four sites in the cells overexpressing Lem4-GFP. Red dashed line indicates the level of phosphorylation in the control GFP-expressing cell line.
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    Image Search Results


    Increased levels of phospho-FGFR1 in cardiomyocytes of diabetic mice. C57BL/6 mice were made diabetic by STZ. Heart tissues were harvested after 20 weeks of disease duration from diabetic (STZ) and non-diabetic control (Ctrl) mice. (A, B) Representative site-specific tyrosine kinase phosphorylation PST228 ProArray showing phosphorylated proteins (A). Magnified images and signal-to-noise ratio (SNR) of FGFR1 (Tyr766) in STZ (red box) and Ctrl (yellow box) are shown in panel (B). (C) Relative abundance of FGFR1 protein in STZ and Ctrl heart tissues from AVK276 Kinase Array were shown. (D) Representative blots showing the levels of p-FGFR1 (Tyr-766) and FGFR1 in heart tissue. GAPDH was used as a loading control. (E) Immunofluorescence staining of mouse heart tissues for p-FGFR1 (red), FGFR1 (red), and α -actinin (green). Sections were counterstained with DAPI (blue). Arrows showing p-FGFR1-positive cells (Scale bar = 50 μm). (F) Levels of p-FGFR1 (Tyr-766) and FGFR1 in primary adult mouse cardiomyocytes and cardiac fibroblasts. Cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control. (G) Levels of p-FGFR1 (Tyr-766) and FGFR1 in rat primary cardiomyocytes. Isolated cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control.

    Journal: Acta Pharmaceutica Sinica. B

    Article Title: Hyperglycemia activates FGFR1 via TLR4/c-Src pathway to induce inflammatory cardiomyopathy in diabetes

    doi: 10.1016/j.apsb.2024.01.013

    Figure Lengend Snippet: Increased levels of phospho-FGFR1 in cardiomyocytes of diabetic mice. C57BL/6 mice were made diabetic by STZ. Heart tissues were harvested after 20 weeks of disease duration from diabetic (STZ) and non-diabetic control (Ctrl) mice. (A, B) Representative site-specific tyrosine kinase phosphorylation PST228 ProArray showing phosphorylated proteins (A). Magnified images and signal-to-noise ratio (SNR) of FGFR1 (Tyr766) in STZ (red box) and Ctrl (yellow box) are shown in panel (B). (C) Relative abundance of FGFR1 protein in STZ and Ctrl heart tissues from AVK276 Kinase Array were shown. (D) Representative blots showing the levels of p-FGFR1 (Tyr-766) and FGFR1 in heart tissue. GAPDH was used as a loading control. (E) Immunofluorescence staining of mouse heart tissues for p-FGFR1 (red), FGFR1 (red), and α -actinin (green). Sections were counterstained with DAPI (blue). Arrows showing p-FGFR1-positive cells (Scale bar = 50 μm). (F) Levels of p-FGFR1 (Tyr-766) and FGFR1 in primary adult mouse cardiomyocytes and cardiac fibroblasts. Cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control. (G) Levels of p-FGFR1 (Tyr-766) and FGFR1 in rat primary cardiomyocytes. Isolated cells were exposed to 33 mmol/L glucose (HG) for 15 min. GAPDH was used as loading control.

    Article Snippet: Kinase Antibody Array Kit (AVK276, including 276 kinase antibodies) and Tyrosine Phosphorylation ProArray (PST228, including 228 site-specific tyrosine phosphorylation antibodies) were obtained from Full Moon Biosystems (Sunnyvale, CA USA) .

    Techniques: Control, Phospho-proteomics, Immunofluorescence, Staining, Isolation

    Effect of Lem4 on tyrosine phosphorylation of signal proteins in HEK293T cell line, as detected by tyrosine phosphorylation ProArray (Full Moon BioSystems). Phosphorylation levels were increased by at least 30% at 30 sites and decreased by at least 30% at four sites in the cells overexpressing Lem4-GFP. Red dashed line indicates the level of phosphorylation in the control GFP-expressing cell line.

    Journal: The Journal of Biological Chemistry

    Article Title: Legionella pneumophila effector Lem4 is a membrane-associated protein tyrosine phosphatase

    doi: 10.1074/jbc.RA118.003845

    Figure Lengend Snippet: Effect of Lem4 on tyrosine phosphorylation of signal proteins in HEK293T cell line, as detected by tyrosine phosphorylation ProArray (Full Moon BioSystems). Phosphorylation levels were increased by at least 30% at 30 sites and decreased by at least 30% at four sites in the cells overexpressing Lem4-GFP. Red dashed line indicates the level of phosphorylation in the control GFP-expressing cell line.

    Article Snippet: Phospho-specific protein microarray analysis Tyrosine phosphorylation ProArray was purchased from Full Moon Biosystems (Sunnyvale, CA).

    Techniques: Phospho-proteomics, Control, Expressing