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. 2022 Feb 16;15:25. doi: 10.1186/s13048-021-00937-3

Table 1.

Primer sequence used in this study

Gene Primer sequence (5′-3′)
OIP5-AS1 F: 5′-TGCTGTGATGCTGGGAACTT-3′
R: 5′-TGGGCTGATTGACCAATCTCA-3’
miR-92a F: 5′-TATTGCACTTGTCCCGGCCTGT-3’
R: mRQ 3’ Primer
ITGA6 F: 5′-GGCGGTGTTATGTCCTGAGTC-3’
R: 5′-AATCGCCCATCACAAAAGCTC-3’
E-cadherin F: 5′-CAGCATCACTGGCCAAGGAGCTGA-3’
R: 5′-GACCACACTGATGACTCCTGTGTTCC-3’
Vimentin F: 5′-CCGACACTCCT ACAAGATTTAGA-3’
R: 5′-CAAAGATTTATTGAAGCAGAACC-3’
U6 F: 5′-GCTTCGGCAGCACATATACTAAAAT-3’
R: 5′-CGCTTCACGAATTTGCGTGTCAT-3’
GAPDH F: 5′-CGGAGTCAACGGATTTGGTCGTAT- 3’
R: 5′-AGCCTTCTCCATGGTGGTGAAGAC-3’

F forward, R reverse, OIP5-AS1, opa-interacting protein 5 antisense transcript 1, miR-92a, microRNA-92a, ITGA6, integrin alpha 6, GAPDH, glyceraldehyde phosphate dehydrogenase, mRQ 3’ Primer were supplied with Mir-X™ miRNA First-Strand Synthesis and SYBR qRT-PCR kit (Takara Bio Inc., Japan)