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. Author manuscript; available in PMC: 2006 Mar 20.
Published in final edited form as: Hum Reprod. 2005 Aug 25;20(12):3360–3368. doi: 10.1093/humrep/dei261

Table 1.

The nucleotide sequences and fluorescent labels of the primers for RT-PCR of LHB/CGB and reference genes.

Gene Primer
F/R Sequence with Fluorescent Dye* Tm (ºC) Product size
CGB } F 5′-GACCCCACCATAGGCAGAG-3′ 61 541bp
CGB5
CGB7 R 5′-GGTAGTTGCACACCACCTGA-3′ FAM 59.4
CGB8
CGB1 } F 5′-GGAGGGAGGAAGGGGAACT-3′ 61 207bp
CGB2
CGB1 RG 5′-GCAACAGCAGCAGCCTCTTT-3′ FAM 59.4
CGB2 RG 5′-CAACAGCAGCAGCCCCTTT-3′ FAM 58.8 206bp
GAPDH FML 5′-CCATGGAGAAGGCTGGGG-3′ 60.5 196bp
RML 5′-CCAAGTTGTCATGGATGACC-3′ HEX 57.3
RPII F 5′-CTTCACGGTGCTGGGCATT-3′ 58.8 239bp
RR 5′-GTGCGGCTGCTTCCATAA-3′ TET 56
LHB** FG 5′-GCTACTGCCCCACCATGATG-3′ 61.4 94bp
R1G 5′-ATGGACTCGAAGCGCACATC-3′ FAM 59.4
R2 5′-AGAGCCACAGGGAAGGAGAC-3′ FAM 61.3 151bp
R3 5′-AGCTGAGAGCCACAGGGAAG-3′ FAM 61.4 156bp

Tm, melting temperature; F, forward primer; R, reverse primer; a primer originally published by

R

Radonic et al.

*

6-FAM, TET and HEX emit fluorescent signals at 532nm, 543nm, 557nm of wavelengths, respectively.

**

For LHB, one forward primer was combined with different reverse primers.