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. 2020 Nov 24;12(12):3499. doi: 10.3390/cancers12123499

Table 1.

Primers for targets selected.

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 2ΔΔCt. A Student’s unpaired t-test was used to calculate statistical significance (p < 0.05).