PRPF38A (Pre-mRNA-splicing factor 38A) antibodies are polyclonal reagents designed to detect and analyze the PRPF38A protein, which plays a transient but essential role in spliceosome activation during RNA splicing . These antibodies enable researchers to investigate PRPF38A's localization, interactions, and functional roles in cellular processes and diseases.
PRPF38A is a B-specific spliceosomal protein incorporated during pre-catalytic spliceosome (B complex) formation and released upon activation . Key findings:
Knockdown Effects: Depletion of PRPF38A increases intron retention, disrupting spliceosome activation and mRNA maturation .
Protein Interactions: Binds transiently with spliceosomal components like MFAP and Snu23, facilitating structural rearrangements during splicing .
PRPF38A is a vulnerability in basal-A triple-negative breast cancer (TNBC):
Functional Studies: siRNA-mediated knockdown of PRPF38A reduced viability in 4/5 basal-A TNBC cell lines by inducing intron retention in transcripts critical for mitosis and apoptosis .
Therapeutic Potential: Splicing modulators (e.g., E7107) targeting PRPF38A-related pathways suppressed TNBC xenograft growth, with enhanced efficacy when combined with proteasome inhibitors .
PRPF38A antibodies have been utilized in:
Subcellular Localization: Demonstrating PRPF38A’s nuclear and nucleolar distribution using immunofluorescence .
Mechanistic Studies: Tracking re-localization to nuclear lamina or nucleoli via chemical dimerizers to study splicing regulation .
Diagnostic Development: Detecting PRPF38A expression in clinical samples (e.g., human tonsil, cervical epithelium) .
Species Cross-Reactivity: Confirmed for human and mouse; potential cross-reactivity with canine tissues requires empirical validation .
Validation: Always include positive controls (e.g., HUVEC or COLO cell lysates) and peptide blocking experiments to confirm specificity .
Storage: Avoid repeated freeze-thaw cycles to maintain antibody stability .