Table 1. Primers used.

Primer	Sequence	Primer	Sequence
NewA	5′-GTGGAGTCTACGCGAACTTGTCCT17–3′	CDK4R822	5′-TCCACATGTCCACAGGTGTTGC-3′
NewC	5′-GTGGAGTCTACGCGAACTTGTCC-3′	CDK4F933	5′-GATGACTGGCCTCGAGATGT-3′
NewB mixture	5′-TCAGGATTGATGGTGCCTACAGC13V-3′ (V = A,G,T)	CDK4R1086	5′-AGGCAGAGATTCGCTTGTGT-3′
NewD	5′-TCAGGATTGATGGTGCCTACAGC-3′	CDK4F1096	5′-TGCAGCACTCTTATCTACATAAGGAT-3′
HPRT1F123	5′-CTTCCTCCTCCTGAGCAGTC-3′	TSPAN31F73	5′-AAGCTGTCGGGGTCCTGGAA-3′
HPRT1R683	5′-AACACTTCGTGGGGTCCTTT-3′	TSPAN31F647	5′-CTTAAGCATTCAGACGAAGC-3′
CCND1F70	5′-TAGCAGCGAGCAGCAGAGTC-3′	TSPAN31R860	5′-ACCCTAGATATTCCCTAAGG-3′
CCND1F183	5′-CCCAGCTGCCCAGGAAGAGC-3′	TSPAN31R1668	5′-CTTGGAAGAAGGGACTTTCC-3′
CCND1R981	5′-TTGACTCCAGCAGGGCTTCG-3′	MYCF125	5′-GCGCTGAGTATATAAAAGCCGGTT-3′
CCND1R1067	5′-TGTGCAAGCCAGGTCCACCT-3′	MYCR838	5′-CCACCGCCGTCGTTGTCTCC-3′
CDK4F136	5′-GTATGGGGCCGTAGGAACCG-3′	BCAS4E1F	5′-TCCTGATGCTGCTCGTGGAC-3′
CDK4F665	5′ TCTGGTGACAAGTGGTGGAA 3′	BCAS3E25R	5′-CATACACAGGGACCGAGCTT-3′
NewDCF933	5′-TCAGGATTGATGGTGCCTACAGCGATGACTGGCCTCGAGATGT-3′
NewDTF647	5′-TCAGGATTGATGGTGCCTACAGCCTTAAGCATTCAGACGAAGC-3′

Note: The number in the primer indicates the first (for forward) or the last (for reverse) nucleotide of that primer in the position of the mRNA. Thus, the range between the F and R numbers should normally be the size of the RT-PCR amplified DNA fragment in agarose gel.