Western Blotting Reagents

Anti-Phospho Enol Pyruvate Carboxylase antibody is suitable for western blotting, IHC and for ELISA. Researchers should determine optimal titers for applications that are not stated below.

Anti-PHOX2B Antibody has been tested for use in ELISA and Western Blotting. Specific conditions for reactivity should be optimized by the end user. Expect a band at approximately 32 kDa in Western Blots of specific cell lysates and tissues.

Anti-PIK3R2 is useful for Immunohistochemistry -P and Western Blotting. Specific conditions for reactivity should be optimized by the end user. Expect a band approximately ~81.5 kDa corresponding to the appropriate cell lysate or extract.

ANTI-PKA C-A CLONE 2E17 ZOOMAB« RABBIT MONOCLONAL

ANTI-PKA C-A CLONE 2E17 ZOOMAB« RABBIT MONOCLONAL

This antiserum has been tested for use in western blotting, immunoprecipitation and immunohistochemistry.  Specific conditions for reactivity should be optimized by the end user.

Anti-PLAC1 Antibody has been tested for use in ELISA, Western Blotting, Immunocytochemistry and Immunofluorescence. Specific conditions for reactivity should be optimized by the end user.

Anti-PLAC3 Antibody has been tested for use in ELISA, Western Blotting, Immunocytochemistry and Immunofluorescence. Specific conditions for reactivity should be optimized by the end user.

Anti-PLAC4 Antibody has been tested for use in ELISA, Western Blotting, Immunocytochemistry and Immunofluorescence. Specific conditions for reactivity should be optimized by the end user.

Anti-PLAGL2 Antibody has been tested for use in ELISA and Western Blotting. Specific conditions for reactivity should be optimized by the end user. Expect a band at approximately 55 kDa in Western Blots of specific cell lysates and tissues.

This affinity purified antibody has been tested for use in ELISA and western blotting.  Specific conditions for reactivity should be optimized by the end user.

Anti-POL II antibody has been tested in ChIP and ELISA, and is likely suitable for western blotting and immunofluorescence assays. Positive controls used in ChIP were EGF stimulated NR4A1 5', NR4A1 3' and FOS 3'.