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rabbit polyclonal anti met antibody c 28  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit polyclonal anti met antibody c 28
    Rabbit Polyclonal Anti Met Antibody C 28, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 415 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+c+met+rabbit+polyclonal+antibody/Met+Antibody/pmc12635195-14-18-23
    Average 94 stars, based on 415 article reviews
    rabbit polyclonal anti met antibody c 28 - by Bioz Stars, 2026-11
    94/100 stars

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    Related Articles

    Immunohistochemical staining:

    Article Title: MET Mutation Is a Potential Therapeutic Target for Advanced Endometrial Cancer
    Article Snippet: .. Immunohistochemical staining for the c-MET protein was performed using the anti-c-MET rabbit polyclonal antibody (sc-161; Santa Cruz Biotechnology). ..

    Staining:

    Article Title: MET Mutation Is a Potential Therapeutic Target for Advanced Endometrial Cancer
    Article Snippet: .. Immunohistochemical staining for the c-MET protein was performed using the anti-c-MET rabbit polyclonal antibody (sc-161; Santa Cruz Biotechnology). ..

    Immunoprecipitation:

    Article Title: Inhibition of Met/HGF receptor and angiogenesis by NK4 leads to suppression of tumor growth and migration in malignant pleural mesothelioma.
    Article Snippet: .. Cancer: 127, 1948–1957 (2010) VC 2010 UICC Immunoprecipitation and Western blot analysis Cells were lysed in buffer containing 50 mM Tris-HCl, pH 7.5, 1% (v/v) Triton X-100, 1% deoxycholic acid, 150 mM NaCl, 2 mM PMSF, 1 mM sodium orthovanadate, 2.5 lg/ml antipain, 5 lg/ml aprotinin, 5 lg/ml pepstatin and 5 lg/ml leupeptin, and the cell debris was removed by centrifugation at 10,000g for 30 min. For immunoprecipitation, the cell lysates were incubated with anti-c-Met rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) for 2 hr, and the immunocomplexes were precipitated with a mixture of protein Aand G-Sepharose. ..

    Western Blot:

    Article Title: Inhibition of Met/HGF receptor and angiogenesis by NK4 leads to suppression of tumor growth and migration in malignant pleural mesothelioma.
    Article Snippet: .. Cancer: 127, 1948–1957 (2010) VC 2010 UICC Immunoprecipitation and Western blot analysis Cells were lysed in buffer containing 50 mM Tris-HCl, pH 7.5, 1% (v/v) Triton X-100, 1% deoxycholic acid, 150 mM NaCl, 2 mM PMSF, 1 mM sodium orthovanadate, 2.5 lg/ml antipain, 5 lg/ml aprotinin, 5 lg/ml pepstatin and 5 lg/ml leupeptin, and the cell debris was removed by centrifugation at 10,000g for 30 min. For immunoprecipitation, the cell lysates were incubated with anti-c-Met rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) for 2 hr, and the immunocomplexes were precipitated with a mixture of protein Aand G-Sepharose. ..

    Centrifugation:

    Article Title: Inhibition of Met/HGF receptor and angiogenesis by NK4 leads to suppression of tumor growth and migration in malignant pleural mesothelioma.
    Article Snippet: .. Cancer: 127, 1948–1957 (2010) VC 2010 UICC Immunoprecipitation and Western blot analysis Cells were lysed in buffer containing 50 mM Tris-HCl, pH 7.5, 1% (v/v) Triton X-100, 1% deoxycholic acid, 150 mM NaCl, 2 mM PMSF, 1 mM sodium orthovanadate, 2.5 lg/ml antipain, 5 lg/ml aprotinin, 5 lg/ml pepstatin and 5 lg/ml leupeptin, and the cell debris was removed by centrifugation at 10,000g for 30 min. For immunoprecipitation, the cell lysates were incubated with anti-c-Met rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) for 2 hr, and the immunocomplexes were precipitated with a mixture of protein Aand G-Sepharose. ..

    Incubation:

    Article Title: Inhibition of Met/HGF receptor and angiogenesis by NK4 leads to suppression of tumor growth and migration in malignant pleural mesothelioma.
    Article Snippet: .. Cancer: 127, 1948–1957 (2010) VC 2010 UICC Immunoprecipitation and Western blot analysis Cells were lysed in buffer containing 50 mM Tris-HCl, pH 7.5, 1% (v/v) Triton X-100, 1% deoxycholic acid, 150 mM NaCl, 2 mM PMSF, 1 mM sodium orthovanadate, 2.5 lg/ml antipain, 5 lg/ml aprotinin, 5 lg/ml pepstatin and 5 lg/ml leupeptin, and the cell debris was removed by centrifugation at 10,000g for 30 min. For immunoprecipitation, the cell lysates were incubated with anti-c-Met rabbit polyclonal antibody (Santa Cruz Biotechnology, Santa Cruz, CA) for 2 hr, and the immunocomplexes were precipitated with a mixture of protein Aand G-Sepharose. ..



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