Additional file 2 of CRISPR-dCas13-tracing reveals transcriptional memory and limited mRNA export in developing zebrafish embryos

Additional file 2: Table S1. List of oligonucleotides and primer sequences used in this study. (A) Primer sequences used in RT-qPCR. (B) Primer sequences for WISH probe template amplification. (C) Sequences of oligonucleotides used in unmodified gRNA. (D) Sequences of oligonucleotides used in modified gRNA. (E) Sequences of oligonucleotides used in smFISH probes. (F) Primer sequences used in clone.

附加文件2：表S1。本研究中使用的寡核苷酸与引物序列列表。(A) 逆转录实时定量聚合酶链反应（RT-qPCR）所用引物序列。(B) 全胚原位杂交（WISH）探针模板扩增所用引物序列。(C) 未修饰向导RNA（guide RNA，gRNA）所用寡核苷酸序列。(D) 修饰向导RNA（gRNA）所用寡核苷酸序列。(E) 单分子荧光原位杂交（smFISH）探针所用寡核苷酸序列。(F) 克隆实验所用引物序列。