TABLE 1

Primer and probe sequences used in quantitative real-time RT-PCR assays to measure mRNA levels of lipogenic genes

Transcript quantitation based on real-time monitoring of amplification was carried out according to the parameters defined under Materials and Methods.

Gene Name or SymbolGenBank Accession No.Primers (5′→3′)TaqMan Probe (5′→3′)
ForwardReverse
SCD1NM_005063CACCTCTTCGGATATCGTCCTGTAGTTGTGGAAGCCCTCACCFAM-ATGACAAGAACATTAGCCCCCGGGAG-BHQ
ACSL1NM_001995AGATCTTGCAGTAATTTGTTTCACAACGCTCACTATGTTTCGGTGAGTFAM-TGGAACTACAGGCAACCCCAAAGGAG-BHQ
DGAT1NM_012079TGGAACATCCCTGTGCACATGCCCCGTCGAAGCATFAM-TGGTGCATCAGACACTTCTACAAGCCC-BHQ
AdfpNM_001122GTGACTGGCAGTGTGGAGAAGTCCGACTCCCCAAGACTGTFAM-CCAAGTCTGTGGTCAGTGGCAGCA-BHQ
PPARγNM_138712ATGCTGGCCTCCTTGATGAGCTTTCGCAGGCTCTTTAGAAFAM-TCTCATATCCGAGGGCCAAGGCTTC-BHQ
CyclophilinNM_021130ACGGCGAGCCCTTGGTTTCTGCTGTCTTTGGGACCTFAM-CGCGTCTCCTTTGAGCTGTTTGCA-BHQ
  • FAM, 5-carboxyfluorescein; BHQ, black hole quencher.