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. 2019 Oct 9;11(10):2409. doi: 10.3390/nu11102409

Table 1.

Primers used in the present study.

Primer Sequence (5′→3′) Reference
ERIC ATGTAAGCTCCTGGGGATTCAC [26]
AAGTAAGTGACTGGGGTGAGCG
BOX CTACGGCAAGGCGACGCTGACG [16]
(GTG)5 GTGGTGGTGGTGGTG [27]
RAPD CTCAGGTCGC Present work
For qRT-PCR Sequence (5′→3′) Size (bp) Accession number
A1R-F AGAACCACCTCCACCCTTCT 227 XM_006529079.2
A1R-R TACTCTGGGTGGTGGTCACA
A2AR-F AACCTGCAGAACGTCAC 245 XM_006513093.3
A2AR-R GTCACCAAGCCATTGTACCG
NT5e-F TTACTAAAGCATGACTCTGGTGATCAA 84 NM_011851.4
NT5e-R AACGGCTGGGTAAACTACTTTCATT
GAPDH-F CAATGTGTCCGTCGTGGATCT 208 XM_017321385.1
GAPDH-R GTCCTCAGTGTAGCCCAAGATG

ERIC, enterobacterial repetitive intergenic consensus; RAPD, random amplification of polymorphic DNA; qRT-PCR, quantitative real-time polymerase chain reaction; A1R, adenosine A1 receptor; A2AR, adenosine A2A receptor; NT5e, 5’ nucleotidase-ecto—enzyme that converts adenosine monophosphate to adenosine; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.