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. 2013 Sep 16;8(9):e74083. doi: 10.1371/journal.pone.0074083

Table 1. Primers used for quantitative real-time PCR analysis.

Gene Forward primer Reverse primer
36b4 GGACCCGAGAAGACCTCCTT GCACATCACTCAGAATTTCAATGG
Arg1 CATGGGCAACCTGTGTCCTT CGATGTCTTTGGCAGATATGCA
Atgl ACAGTGTCCCCATTCTCAGG TTGGTTCAGTAGGCCATTCC
B2-microglobulin TGACCGGCTTGTATGCTATC CAGTGTGAGCCAGGATATAG
Ccl5 GGAGTATTTCTACACCAGCAGCAA GCGGTTCCTTCGAGTGACA
Cd163 CTCAGGAAACCAATCCCAGA CAAGAGCCCTCGTGGTAGAC
Cd36 GCAAAGAACAGCAGCAAAATC CAGTGAAGGCTCAAAGATGG
Hsl AGACACCAGCCAACGGATAC ATCACCCTCGAAGAAGAGCA
Il10 TTTGAATTCCCTGGGTGAGAA CTCCACTGCCTTGCTCTTATTTTC
Mrc1 GAGAGCCAAGCCATGAGAAC GTCTGCACCCTCCGGTACTA
Nos2 CGGGCATCTGGTAGCCAGCG TGGCAACATCAGGTCGGCCAT
Soc1 CCGTGGGTCGCGAGAAC AAGGAACTCAGGTAGTCACGGAGTA
Tnf GGCAGGTCTACTTTGGAGTCATTGC ACATTCGAGGCTCCAGTGAATTCGG
Ucp1 TCAGGATTGGCCTCTACGAC TGCATTCTGACCTTCACGAC

Arg1, arginase 1; Atgl, adipose triglyceride lipase; Ccl5, Chemokine (C–C motif) ligand 5;

Hsl, hormone-sensitive lipase; Il10, interleukin-10; Mrc1, mannose receptor 1; Nos2,

nitric oxide synthase 2; Tnf, tumor necrosis factor-α Ucp-1,uncoupling protein-1.