Key result
Three commercially available AT2 receptor antibodies (2818-1, sc-9040, and AAR-012) were found to be nonspecific, demonstrating identical immunoreactive patterns in tissues from both wild-type and AT2 receptor knockout mice.
Commercially available AT2 receptor antibodies lack specificity, highlighting the need to rely on competitive radioligand binding and mRNA expression for studying AT2 receptor expression.
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Nonspecific AT2 antibodies should not be used; challenges prior receptor localization studies and leaves validation needs open.
Commercially available angiotensin II At₂ receptor antibodies are widely employed for receptor localization and quantification, but they have not been adequately validated. In this study, we characterized three commercially available At₂ receptor antibodies: 2818-1 from Epitomics, sc-9040 from Santa Cruz Biotechnology, Inc., and AAR-012 from Alomone Labs. Using western blot analysis the immunostaining patterns observed were different for every antibody tested, and in most cases consisted of multiple immunoreactive bands. Identical immunoreactive patterns were present in wild-type and At₂ receptor knockout mice not expressing the target protein. In the mouse brain, immunocytochemical studies revealed very different cellular immunoreactivity for each antibody tested. While the 2818-1 antibody reacted only with endothelial cells in small parenchymal arteries, the sc-9040 antibody reacted only with ependymal cells lining the cerebral ventricles, and the AAR-012 antibody reacted only with multiple neuronal cell bodies in the cerebral cortex. Moreover, the immunoreactivities were identical in brain tissue from wild-type or At₂ receptor knockout mice. Furthermore, in both mice and rat tissue extracts, there was no correlation between the observed immunoreactivity and the presence or absence of At₂ receptor binding or gene expression. We conclude that none of these commercially available At₂ receptor antibodies tested met the criteria for specificity. In the absence of full antibody characterization, competitive radioligand binding and determination of mRNA expression remain the only reliable approaches to study At₂ receptor expression.
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Hafko et al. (2013) studied this question. Commercially available Angiotensin II AT2 receptor antibodies vs. AT2 receptor knockout mice and tissues not expressing AT2 receptors was evaluated on Antibody specificity evaluated by western blot and immunocytochemistry. Three commercially available AT2 receptor antibodies (2818-1, sc-9040, and AAR-012) were found to be nonspecific, demonstrating identical immunoreactive patterns in tissues from both wild-type and AT2 receptor knockout mice.
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