RXRA expression in HeLa nuclear cell lysate (A) + peptide (B) and nuclear K562 cell lysate (C) + peptide (D) analyzed by western blot. Cells were lysed in RIPA buffer and 35µg protein was run per lane. Primary antibody incubation was performed with Anti-RXRA Antibody (A83409) at 0.3µg/ml and detected by chemiluminescence.
RXRA expression in MCF7 cells analyzed by immunofluorescence. Cells were permeabilized with 0.15% Triton. Staining was performed with Anti-RXRA Antibody (A83409) at 10µg/ml for 1 hour and Alexa Fluor 488 secondary antibody at 2µg/ml. Strong nuclear staining shown and nuclei were stained with DAPI (blue) while actin filaments were stained with phalloidin (red). Negative control: Goat IgG Isotype Control at 10µg/ml followed by Alexa Fluor 488 secondary antibody at 2µg/ml.
RXRA expression in MCF7 cells (blue line) analyzed by flow cytometry. Cells were fixed in PFA and permeabilized with 0.5% Triton. Staining was performed with Anti-RXRA Antibody (A83409) at 10µg/ml for 1 hour and Alexa Fluor 488 secondary antibody at 1µg/ml. Negative Control: Goat IgG Isotype Control (black line) followed by Alexa Fluor 488 secondary antibody.
Publishing research using Anti-RXRA Antibody (A83409)? Please let us know so that we can list the citation on this page.
Proteins predicted to interact with RXRA
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.
