Table 1 of Jin, Mol Vis 2009; 15:523-533.

Table 1. Primer and probe sequences.

Primer/probe Sequence (5′-3′)
F1 CGTTCTTCGGACGCCTCGTCAACAC
F2 GGATCCGTTCTTCGGACGCCTCGTC
A3 TCAGAAGCTATACGGCACAGCCAG
108–03K-F GGACCATACAGGCCGAAGGAC
Neo-R1 CCTTCTATCGCCTTCTTGACGAGTTC
182-R4 CCCAAGTCCTTTTCACCGAGAAGAG
miR182LNA tgTgaGttCtaCcaTtgCcaAa
miR182LNA/MM tgTgaGttCtaCcaAtgCcaAa

Primers used for genotyping the miR-182 KO mice are shown. The perfect-matched LNA-probe against miR-182 (miR182LNA) or the single-base mismatched control probe (miR182LNA/MM) was used for in situ hybridization. LNA positions are in capital letters, with DNA in lower case and the position of the single-base substitution in bold print.

Jin, Mol Vis 2009; 15:523-533. http://www.molvis.org/molvis/v15/a53

©2009 Molecular Vision http://www.molvis.org/molvis/

ISSN 1090-0535