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Rabbit polyclonal anti p53 proteins

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Rabbit polyclonal anti-P53 proteins is a laboratory reagent used for the detection and analysis of p53 proteins. It is produced by immunizing rabbits with p53 proteins, resulting in the generation of a pool of antibodies that recognize various epitopes on the p53 protein. This product can be used in techniques such as Western blotting, immunohistochemistry, and immunoprecipitation to identify and quantify p53 expression in biological samples.

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2 protocols using rabbit polyclonal anti p53 proteins

1

Western Blot Analysis of Apoptosis Markers

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After evaluating the effects of direct, indirect, and combined therapy on proliferation and apoptosis, several proteins activation such as p53, Bax, Bcl-2 and β-Actin were investigated by western blotting. Half of the tumors were extracted from the animals, to determine the protein level in tissue of all groups. To perform this analysis, tissues were washed twice with PBS, then squished and combined with buffer and centrifuged for 15 minutes. The protein concentration was determined by applying the Bradford method. The proteins were dissevered by electrophoresis with sodium dodecyl sulfate-polyacrylamide gel (SDS-PAGE) and then transferred onto polyvinylidene difluoride (PVDF). Finally, they were investigated with primary antibody including rabbit polyclonal anti-Bax (1:200), mouse polyclonal anti-Bcl2 (1:200), rabbit polyclonal anti-P53 proteins (1:200) (Santa Cruz Biotechnology, USA) and secondary antibodies conjugated with horse radish peroxidase (HRP) (Cell Signaling Technology, USA).the β-Actin generation signal was used as an internal control.
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2

Western Blot Analysis of Apoptosis Markers

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For western blotting analysis half of the tumors were collected from the animals. Extraction of proteins from samples were performed by RIPA buffer (10 mM Tris–HCl, pH 7.4, 150 mM NaCl, 5 mM EDTA, 1% Triton X-100, 0.1% sodium dodecyl sulfate and 0.5% Sodium deoxycholate) containing protease and phosphatase inhibitor cocktails. Protein concentrations were examined by Bradford assay50 . Equal amounts of the total proteins were run on 12% Sodium dodecyl sulfate-polyacrylamide gel (SDS-PAGE assay) and transferred to the polyvinylidene difluoride (PVDF) and then probed with specific primary antibodies including rabbit polyclonal anti-Bax (1:200), mouse polyclonal anti-Bcl2 (1:200), rabbit polyclonal anti-P53 proteins (1:200) (Santa Cruz Biotechnology, USA) and secondary antibodies conjugated with horse radish peroxidase (HRP) (Cell Signaling Technology, USA). β-Actin was used as the control. Blots were developed by using DAB (Diaminobenzidine) staining.
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