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Table 1 Primer and probe sequences used for quantitative RT-PCR analysis

From: Activation of the transcription factor, nuclear factor kappa-B, during the estrous cycle and early pregnancy in the pig

Targeta

Forward/Reverse Primers (5' → 3')b

Fluorescent Reporterc

Length of Amplicond

GenBank Accession #e

TNFRSF11A

GCTGACTCTGGAAGAGAAGGTGTT

ATGTGCTGTCCAGACGGTGGTGGTGCCTGT

192 bp

CB475057

 

GCCCTGTCCACATATTCGTCTTCTGT

   

TLR4

ATGGCCTTTCTCTCCTGCCTGA

ATCTGAGAGCTGGGACCCTTGCGTGCAGGT

139 bp

AB188301

 

AGGTCCAGTATCTTGACTGATGTGGG

   

NFKB1

CCCATGTAGACAGCACCACCTATGAT

ACCAGGCTGGCAGCTCTCCTCAAAGCAGCA

132 bp

NM_001048232

 

ACAGAGGCTCAAAGTTCTCCACCA

   

RELA

ACATGGACTTCTCAGCCCTTCTGA

ACACCTGCTCTGCCCAGAGCACTGGGTT

168 bp

CN155798

 

CCGAAGACATCACCCAAAGATGCT

   

NFKBIA

TGTGATCCTGAGCTCCGAGACTTT

TCTACACCTTGCCTGTGAGCAGGGCTGCCT

143 bp

NM_001005150

 

TTGTAGTTGGTGGCCTGCAGAATG

   

NFKBIB

TCATTCTGCAGGTCCAGGTACTCA

TGGATTTCCTCCTGGGCTTTGCTGCTGGCA

89 bp

AK231853

 

CACTTGGCGGTGATTCATCAGCAT

   
  1. aThe amplification target: TNFRSF11A, Receptor activator of NFKB; TLR4, Toll-like receptor 4; NFKB1; RELA, NFKBIA and NFKBIB, Inhibitors of κB α and β, respectively.
  2. bThe forward and reverse DNA oligos used in the amplification of the target. Forward and reverse do not necessarily indicate the in vivo direction of transcription.
  3. cThe DNA oligo sequence of the dual-labeled probe (possessing the FAM reporting dye on the 5' end and the TAMRA quenching dye on the 3' end) used to measure amount of amplified target during each cycle of quantitative RT-PCR.
  4. dThe length of the amplicon created during PCR.
  5. eThe accession number to the porcine sequence that was utilized during primer and probe design.