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. 2016 May 10;25(13):959–974. doi: 10.1089/scd.2016.0010

Table 2.

Short Hairpin Sequences Against Id2 RNA Used in This Study

SiRNA Sense sequences Loop Antisense sequence Targets
Id2-96 T5′gatgagtctgctctacaaca ttcaagaga tgttgtagagcagactcatc3′ 96–115
  B5′gatgagtctgctctacaaca tctcttgaa tgttgtagagcagactcatc3′  
Id2-369 T5′gcttatgtcgaatgatagca ttcaagaga tgctatcattcgacataagc3′ 369–388
  B5′gcttatgtcgaatgatagca tctcttgaa tgctatcattcgacataagc3′  
Id2-96s T5′gtcgataccttagactcaga ttcaagaga tctgagtctaaggtatcgac3′ Scrambled
  B5′gtcgataccttagactcaga tctcttgaa tctgagtctaaggtatcgac3′  
Id2-369s T5′gatttcggatcagaacatgt ttcaagaga acatgttctgatccgaaatc3′ Scrambled
  B5′gatttcggatcagaacatgt tctcttgaa acatgttctgatccgaaatc3′  

The number after Id2 indicates the first coding region nucleotide recognized by the siRNA. Sense and antisense DNA sequences for the top (T) strand and the bottom (B) strand oligos, loop regions, and complete Id2 coding region targeted by the siRNA are shown. The Id2 shDNA sequences against the coding region of the mouse Id2 gene used in this study were generated using the siRNA Wizard™ and Block-iT™ RNAi designers and confirmed by NCBI nucleotide Blast.