<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>Geisel School of Medicine at Dartmouth</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA257063</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>The animal replication-dependent (RD) histone mRNAs are coordinately regulated with chromosome replication. They are the only known cellular mRNAs that are not polyadenylated. Instead, the mature transcripts end in at a conserved stem-loop (SL) structure. This SL structure interacts stably with the stem-loop binding protein (SLBP), which is involved in all aspects of RD-histone mRNA metabolism. We used several genomic methods, including RNA Binding Protein IP followed by microarray analysis (RIP-ChIP) to analyze the RNA binding landscape of SLBP. Overall design: Reference based design on two color Agilent DNA microarrays. Experimental sample is labeled in Ch1 (Cy3), which are mRNA bound by the SLBP RNA-binding protein. The reference sample is labeled in Ch2 (Cy5) which are the polyribosomal mRNAs from the supernatant that were not bound by anti-SLBP. Controls included no antibody in the IP (which tends to have non-specific background binding to the beads) and pre-incubation of the SLBP with the antibodies antigenic peptide, which blocks antibody binding to the SLBP.</long_description><tag>xref:PubMed:26377992</tag><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Homo sapiens</name><description>Anti-SLBP RIPchip data</description><dates><last_updated>2025-09-24</last_updated><first_public>2024-04-04</first_public></dates><accession>PRJNA257063</accession><cross_references><GEO>GSE59915</GEO><taxon>9606</taxon><PubMed>26377992</PubMed></cross_references></HashMap>