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c met primary antibody  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc c met primary antibody
    C Met Primary Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 431 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/c+met+primary+antibody/Met+XP+Rabbit+mAb/pm41402584-479-18-21
    Average 96 stars, based on 431 article reviews
    c met primary antibody - by Bioz Stars, 2026-09
    96/100 stars

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    Incubation:

    Article Title: Single-cell and spatial transcriptomic characterization of pulmonary pleomorphic carcinoma.
    Article Snippet: .. Sectionswere thenblocked with 2.5% Normal Horse Serum (Vector Laboratories) for 20min and incubated overnight at 4 °Cwith a c-MET primary antibody (Cell Signaling Technology; Cat. #8198; dilution 1:150). .. Sectionswere incubated for 30min with the ImmPRESS VR Polymer HRP Anti-Rabbit IgG Reagent (Vector Laboratories).

    Article Title: Single-cell and spatial transcriptomic characterization of pulmonary pleomorphic carcinoma
    Article Snippet: .. Sections were then blocked with 2.5% Normal Horse Serum (Vector Laboratories) for 20 min and incubated overnight at 4 °C with a c-MET primary antibody (Cell Signaling Technology; Cat. #8198; dilution 1:150). .. Sections were incubated for 30 min with the ImmPRESS VR Polymer HRP Anti-Rabbit IgG Reagent (Vector Laboratories).



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    Inhibition of FGFR1 activation and downstream signaling by AZD4547 were dependent on the EOC cell lines and chemo-sensitive PDX. AZD4547 was applied for different durations in EOC cells. Phospho-FGFR1 and phosphorylation of downstream signaling proteins including p-AKT and <t>p-ERK</t> were investigated in cell lysates and tumor lysates obtained from AZD4547-treated PDX mice compared with control-treated mice by western blot analysis. β-actin was used as a loading control
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    Inhibition of FGFR1 activation and downstream signaling by AZD4547 were dependent on the EOC cell lines and chemo-sensitive PDX. AZD4547 was applied for different durations in EOC cells. Phospho-FGFR1 and phosphorylation of downstream signaling proteins including p-AKT and p-ERK were investigated in cell lysates and tumor lysates obtained from AZD4547-treated PDX mice compared with control-treated mice by western blot analysis. β-actin was used as a loading control

    Journal: Cancer Cell International

    Article Title: The anti-tumor effects of AZD4547 on ovarian cancer cells: differential responses based on c-Met and FGF19/FGFR4 expression

    doi: 10.1186/s12935-024-03235-2

    Figure Lengend Snippet: Inhibition of FGFR1 activation and downstream signaling by AZD4547 were dependent on the EOC cell lines and chemo-sensitive PDX. AZD4547 was applied for different durations in EOC cells. Phospho-FGFR1 and phosphorylation of downstream signaling proteins including p-AKT and p-ERK were investigated in cell lysates and tumor lysates obtained from AZD4547-treated PDX mice compared with control-treated mice by western blot analysis. β-actin was used as a loading control

    Article Snippet: The blots were probed using primary antibodies against FGFR1, FGFR2 (Santa Cruz Biotechnology, USA), FGFR3, FGFR4 (Abcam), phospho-FGFR1 (p-FGFR1), total-c-Met, phospho-c-Met (p-c-Met), total-AKT, phospho-AKT (p-AKT), total-ERK, phospho-ERK (p-ERK) (Cell Signaling Technology), or β-actin (Santa Cruz Biotechnology).

    Techniques: Inhibition, Activation Assay, Phospho-proteomics, Control, Western Blot