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Mouse monoclonal anti adar2 antibody

Manufactured by Santa Cruz Biotechnology

Mouse monoclonal anti-ADAR2 antibody is a laboratory tool used to detect and study the ADAR2 protein in biological samples. ADAR2 is an enzyme involved in the process of RNA editing.

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2 protocols using mouse monoclonal anti adar2 antibody

1

Immunoblotting of ADAR Enzymes in Mouse Tissues

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Tissue lysates from mouse cerebral cortex and spleen were prepared and stored at −80°C until use as described previously (Miyake et al. 2016 (link)). Lysates were then separated using sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE), transferred to a polyvinylidene difluoride (PVDF) membrane (Bio-Rad, Hercules) and immunoblotted with primary antibodies using a SNAP i.d 2.0 Protein Detection System (Merck Millipore) as previously described (Nakahama et al. 2018 (link)). The primary antibodies used were as follows: mouse monoclonal anti-ADAR1 antibody (15.8.6; Santa Cruz Biotechnology), mouse monoclonal anti-ADAR2 antibody (1.3.1; Santa Cruz Biotechnology), and mouse monoclonal anti-GAPDH (M171-3; MBL).
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2

Western Blot Analysis of RNA-Editing Enzymes

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Each lysate was separated by SDS-polyacrylamide gel electrophoresis and transferred to polyvinylidene difluoride membranes (Bio-Rad). Immunoblotting was performed by using the following primary antibodies: mouse monoclonal anti-ADAR1 antibody (catalog no.: 15.8.6; Santa Cruz Biotechnology), mouse monoclonal anti-ADAR2 antibody (catalog no.: 1.3.1; Santa Cruz Biotechnology), rabbit polyclonal anti-AZIN1 antibody (catalog no.: 11548-1-AP; Proteintech), mouse monoclonal anti-GFP antibody (catalog no.: GF200; Santa Cruz Biotechnology), rabbit polyclonal anti-Halo Tag antibody (catalog no.: G 928A; Promega), and mouse monoclonal anti-GAPDH antibody (catalog no.: M171-3; MBL). Chemiluminescence was detected by using ImmunoStar Zeta (Fujifilm) or Pierce ECL Western Blotting Substrate (Thermo Fisher Scientific).
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