Skip to main content

Table 3 Copy number aberrant genes analyzed by qRT-PCR

From: A cultured approach to canine urothelial carcinoma: molecular characterization of five cell lines

Gene

Location

Forward primer

Reverse primer

RNPC3

chr6:50072550-50098045

5′-GGGGCGACCGGCCCTTCTA-3′

5′-GACAGGACGCGCACCGACTG-3′

MDM2

chr10:13920606-13946580

5′-ACGGCAGAGAAAGCGCCACAAA-3′

5′-GGCGTCCCTGTTGACTCACTG-3′

EIF2C2

chr13:38222456-38271623

5′-CAAAGGCAGTCCAGGTTCAT-3′

5′-GGGCATCTGTTGGTCTGAGT-3′

RALB

chr19:32842484-32862087

5′-GTGTTCTTGCTCTCCCCAAC-3′

5′-TCCAAAACCTCCCAACAAAG-3′

CLNS1A

chr21:24140052-24163815

5′-CCTGTGTCTCCGCGCTCCCTG-3′

5′-GCCTCGGTCTCGGGCTGCTG-3′

STX19

chr33:4727847-4728760

5′-CTGCTATGTTCCGCCAATTT-3′

5′-GCACTTCTTTTCCAGCAACC-3′

TAGLN2

chr38:25240217-25241796

5′-TGCGGACCTGGAGCAGATCCTG-3′

5′-ACACAGCACCGTGCCATCCT-3′

RPL32

chr18:10198892-10204028

5′-ATGCCCAACATTGGTTATGG-3′

5′-ATGCCCAACATTGGTTATGG-3′

  1. The mRNA levels of genes located within seven regions of copy number aberration were evaluated by qRT-PCR. The targeted gene, genomic location (CanFam2.0 assembly), and primer pair utilized are shown