FBXO11 mediates the degradation of proteins like BCL6, DTL/CDT2, and SNAI1, influencing processes such as B-cell differentiation, TGF-β signaling, and epithelial-to-mesenchymal transition . Its dysregulation has been implicated in inflammation, antiviral responses, and erythropoiesis .
FBXO11 antibodies are polyclonal or monoclonal reagents designed to bind specifically to FBXO11, enabling its detection via techniques like Western blot (WB), immunoprecipitation (IP), and immunofluorescence (IF). Key characteristics include:
Immunogen: Synthetic peptides or recombinant FBXO11 fusion proteins .
Reactivity: Primarily human, with cross-reactivity reported in mouse and rat .
FBXO11 antibodies are validated for diverse experimental workflows, as summarized below:
WB Optimization: Dilutions vary widely; titration is recommended .
IP Efficiency: Requires 0.5–4.0 µg antibody per 1–3 mg lysate .
IF Specificity: Detects nuclear localization in human cell lines .
FBXO11 antibodies have been pivotal in elucidating its biological roles:
FBXO11 regulates C5aR1 (complement receptor) and IL-1β expression in macrophages:
C5aR1 Regulation: Loss of FBXO11 reduces C5aR1 mRNA and surface expression, protecting macrophages from Panton-Valentine leukocidin (PVL)-mediated toxicity .
IL-1β Modulation: FBXO11 dampens IL-1β secretion post-NLRP3 activation via BCL-6-dependent pathways .
Erythroid Development: FBXO11 degrades BAHD1, a repressor of erythroid genes, promoting red blood cell maturation .
MHC-II Expression: FBXO11 targets CIITA for degradation, modulating MHC-II levels critical for immune responses .
TRAF3 Ubiquitination: FBXO11 mediates Lys-63-linked ubiquitination of TRAF3, enhancing TBK1-IRF3-IFN-I signaling during antiviral responses .