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Antimouse or anti rabbit ig horseradish peroxidase secondary antibodies

Manufactured by GE Healthcare
Sourced in Italy

Antimouse or anti-rabbit Ig/Horseradish peroxidase secondary antibodies are laboratory reagents designed to detect and visualize target proteins in various immunoassay techniques. These antibodies are conjugated with the enzyme horseradish peroxidase, which can catalyze a chromogenic reaction, allowing for the specific detection and quantification of the target analyte.

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2 protocols using antimouse or anti rabbit ig horseradish peroxidase secondary antibodies

1

Western Blot Analysis of VEGFR-1 and ERK

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Proteins were run in 10% SDS‐polyacrylamide gels and transferred to supported nitrocellulose membranes by standard techniques. Membranes were incubated with the mouse monoclonal anti‐VEGFR‐1 (clone D2, 1:500; Santa Cruz Biotechnology), rabbit polyclonal anti‐Erk1&2 (1:1000; Genetex), rabbit polyclonal anti‐phospho‐Erk1&2 (Thr/Tyr185/187, 1:1000; Invitrogen) or rabbit polyclonal anti‐β‐tubulin (1:10 000; Santa Cruz Biotechnology) as primary antibodies. Immunodetection was performed using antimouse or anti‐rabbit Ig/Horseradish peroxidase secondary antibodies and ECL Western blotting detection reagents from GE Healthcare (Milan, Italy).
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2

Western Blot Analysis of VEGFR-1 and EGFR

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Proteins were run in 10% SDS-polyacrylamide gels and transferred to supported nitrocellulose membranes by standard techniques. Immunodetection was performed using the following antibodies: mouse monoclonal anti-VEGFR-1 (clone D2, 1:500; Santa Cruz Biotechnology, Santa Cruz, CA); mouse monoclonal anti-EGF receptor (EGFR) (528, 1:1000; Santa Cruz Biotechnology); mouse monoclonal antibody anti-EGFRvIII (L8A4; 1:1000; Absolute Antibody, Oxford, UK); rabbit polyclonal anti-phosphorylated VEGFR-1 at tyrosine 1213 (1:500; R&D Systems); rabbit polyclonal anti-Erk1&2 (1:1000; Genetex, Irvine, CA); rabbit polyclonal anti-phospho-Erk1&2 (Thr/Tyr185/187, 1:1000; Invitrogen); or rabbit polyclonal anti-β-actin (1:10,000; Sigma Aldrich) primary antibodies. Anti-mouse or anti-rabbit Ig/Horseradish peroxidase secondary antibodies and ECL Western blotting detection reagents from GE Healthcare (Milan, Italy) were used to identify the proteins of interest.
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