Fig. 4From: Identification and characterization of ARID1A-interacting proteins in renal tubular cells and their molecular regulation of angiogenesisValidation of the association between ARID1A and its interactor. Cellular proteins from MDCK cells were immunoprecipitated with anti-ARID1A (IP) A, B or anti-β-actin (reciprocal IP) C, D, whereas those parallelly immunoprecipitated with isotype IgG served as the control for all samples. The immunoprecipitated proteins were then resolved by SDS-PAGE and subjected to immunoblotting to detect ARID1A or β-actin. WCL = whole cell lysateBack to article page