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Table 2 Primers designed for the analysis of WNT4 expression by PCR

From: Differential expression of WNT4 in testicular and ovarian development in a marsupial

Primers

Sequence(5'→3')

Function

R1

AGCCTGACCATTGGAAGCCCTCT

5'RACE T-PCR

R2

GCCGCACAGAGTCCATCAC

5'RACE

F1

CATCGAGGAGTGCCAGTACCAGTTT

3'RACE

F2

GACGGTGGAACTGCTCGACTCTG

3'RACE T-PCR

SMART IV

AAGCAGTGGTATCAACGCAGAGTGGCCATTACGGCCGGG

5'RACE

CDS III

ATTCTAGAGGCCGAGGCGGCCGACATG-d(T)30N-1N (N = A, G, C, or T; N-1 = A, G, or C)

3'RACE

5' PCR Primer

AAGCAGTGGTATCAACGCAGAGT

5'RACE

qF

GAAACCGACGGTGGAAC

qPCR

qR

AGGAGATGGCATAGACGAA

qPCR

18S F

GATCCATTGGAGGGCAAGTCT

RT-PCR & qPCR

18S R

CCAAGATCCAACTACGAGCTTTTT

RT-PCR & Qpcr

csF1

GTCATCGGTGGGCAGCATCTC

Cross species cloning

csR1

CGTGACACTTGCACTCCACCC

Cross species cloning

  1. F, forward primers in the 5' to 3'; R, reverse primers in the 3' to 5' direction. q, quantitative PCR primers for real time analysis; CDS, Smart IV and 5'PCR were synthesized by SIGAMA (Genosys) according to the manual of the SMART cDNA library construction kit from Clontech.