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2 protocols using rabbit anti relb

1

Antibody Reagents for Protein Analysis

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The following antibodies were used in this study: rabbit anti-RelA, rabbit anti-RelB (Santa Cruz Biotechnology, Santa Cruz, CA), rabbit anti-Histone H3, rabbit anti-IκBα (Cell Signaling Technology, Danvers, MA), mouse anti-GSH (Virogen, Watertown, MA), mouse anti-IKKα (Upstate, Millipore, Billerica, MA) Streptavidin conjugated-HRP (Jackson, West Grove, PA), goat anti-Grx1 (American Diagnostica, Stamford, CT) and mouse anti-β-actin (Sigma-Aldrich, Saint Louis, MO). The secondary HRP conjugated anti-rabbit and anti-mouse antibodies were from Amersham (Piscataway, NJ), anti-goat was from Jackson Laboratories (West Grove, PA). All fluorophore-conjugated antibodies were from Invitrogen (Carlsbad, CA).
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2

Western Blot Analysis of RELB, p100/p52, AKT

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Purified B cells were subjected to NP40-based lysis, separated by SDS-PAGE and blotted on nitrocellulose membranes (GE Healthcare). Samples were incubated with the following primary antibodies overnight at 4°C: rabbit anti-RELB (Santa Cruz, clone: C-19), rabbit anti-p100/p52 (Cell Signaling Technologies, CST), mouse anti-β-actin (Sigma, clone: AC-15), rabbit anti-pAKT (Cell Signalling, clone: D9E) and rabbit anti-AKT (CST) Horseradish peroxidase-conjugated secondary antibodies and ECL Western Blotting Substrate or SuperSignal West Dura Extended Duration Substrate (Thermo Scientific) were used for detection.
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