The Aryl-Hydrocarbon Receptor Protein Interaction Network (AHR-PIN) as Identified by Tandem Affinity Purification (TAP) and Mass Spectrometry
Independent protein interaction verification. Coimmunoprecipitations (Co-IP) using anti-AHR or normal rabbit IgG as negative control were performed in wild type Hepa1c1c7 cells. (a) Western blot probed with anti-MRPL40 (Invitrogen). (b) Positive control, western blot probed with anti-AHR. MRPL40 and AHR control all show marked enrichment in the AHR pulldown lanes over the IgG control lane.
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