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. 2012 May 4;153(7):3457–3467. doi: 10.1210/en.2011-1921

Table 1.

Primers used for real-time PCR

Gene symbol Sequence References
Glut1 Forward, CCAGCTGGGAATCGTCGTT 38
Reverse, CAAGTCTGCATTGCCCATGAT
Glut3 Forward, CTCTTCAGGTCACCCAACTACGT 38
Reverse, CCGCGTCCTTGAAGATTCC
Snat1 Forward, GATTTACAGGACATTTTTGACCACATAGTA 39
Reverse, CACCTGTACTAGAAGGTGGACCATTT
Snat2 Forward, AGAAGCCATCTTTGATCAAATTGTG 39
Reverse, GACCTGAACTAGAAGGTGAATCATGC
Snat4 Forward, TCACACTGCTGTTTCCAAGG a
Reverse, CAGCCGGAAGAATGAAAATC
Slc7a3 Forward, TTCTGGCCGAGTTGTCTATGTTTG c
Reverse, AGTGCGGTTCTGTGGCTGTCTC
11betaHsd2 Forward, CTGCAGATGGATCTGACCAA 40
Reverse, GTCAGCTCAAGTGCACCAAA
Igf2 Forward, AAGAGTTCAGAGAGGCCAAACG 38
Reverse, CACTGATGGTTGCTGGACATCT
igf2P0 Forward, CCGAGGCCTGTACCACCTA 21
Reverse, CCTCGGCTCAGACCTCAGTA
H19 Forward, AATGGTGCTACCCAGCTCAT a
Reverse, GCAGAGTTGGCCATGAAGAT
Gapdh Forward, ACAACTTTGGCATTGTGGAA b
Reverse, GATGCAGGGATGATGTTCTG
a

Designed using the Primer3 web program http://frodo.wi.mit.edu/primer3/.

b

Designed using the PrimerSelect, DNASTAR lasergene software (Madison, WI).

c

Designed using PerlPrimer program http://perlprimer.sourceforge.net/.