Table 1.
Primer | Sequence 5′–3′ |
---|---|
18S RNA-Forward | ATGGCCGTTCTGAGTTGGTG |
18S RNA-Reverse | CGCTGAGCCAGTCAGTGTAG |
PRKCQ-Forward | CTTGTGGCAGCTTTGGATGT |
PRKCQ-Reverse | CGTTTCTGACGCACATGTTT |
NrCAM-Forward | TTGTGCAAAGAGGGAGCATG |
NrCAM-Reverse | GGGCAGTTCCCTGTTGTCCT |
CDKN1A-Forward | GCAGACCAGCATGACAGATTT |
CDKN1A-Reverse | GGATTAGGGCTTCCTCTTGGA |
RHOH Forward | GAGAAGTAACATTCTGCAAATCGC |
RHOH Reverse | AGCACACGCCATTCAGCAAG |
XIST-Forward | AGGTCAGGCAGAGGAAGTCA |
XIST-Reverse | AGGTCAGGCAGAGGAAGTCA |
ROX1-AS1 Forward | CTAGTTAGCAGGGGCAGCAC |
PROX1-AS1 Reverse | AACAGAGAGGCGTGGAAGAA |
MYC-Forward | TGGACATCCGCAAAGACCTGTAC |
MYC-Reverse | TCAGGAGGAGCAATGATCTTGA |
SFTA1P-Forward | CAGCATTCCAGGTGGGCTTT |
SFTA1P-Reverse | CCTTGTTTGGCTTACTCGTGC |
qPCR data of relative gene expression was analyzed using the ΔΔCt method whereby the endogenous control Ct is subtracted from the gene of interest Ct to calculate ΔCt, and a relative quantity value was calculated by finding 2−ΔΔCt. A Student’s unpaired t-test was used to calculate statistical significance (p < 0.05).