Deciphering Runx1 interacted RNAs during definitive hematopoiesis by ultra-low-input RIP-seq
收藏NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP394234
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资源简介：
our work established a powerful method for physically studying TF-RNA interaction in very few cells, and provide valuable recourse for decoding more precious regulatory network of Runx1 during embryonic hematopoiesis. Overall design: E10.0 caudal half Cd31+ cells form C57BL/6 mice were isolated by Fluorescence-activated cell sorting (FACS) and analyzed using RUNX1 RIP-seq
创建时间：
2022-08-26
