Skip to main content
. 2019 May 21;10:292. doi: 10.3389/fendo.2019.00292

Table 1.

Primer sequences used to amplify IsILP sequences for confirmation by Sanger sequencing or for relative quantification by qRT-PCR.

Primer Nucleotide sequence
SEQUENCING PRIMERS
NotI d(T)2 AACTGGAAGAATTCGCGGCCGCAGGAATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTVN
NotI-d(T) AACTGGAAGAATTCGCGGCCGCAGGAATTTTTTTTTTTTTTTTTT
ILP1F2 GATCGGTCAGCGACTGTTTC
ILP1Fwd5 TTTCCTGGGCACTCAACAC
ILP1R210 GGACACCAGAGGAAACAGTC
ILP3F3 TGCTCGACTTCCTCTGTGAAG
ILP3R3 CAGTACGCGAGAAGCTCCAG
ILP4F2 CTCTAGCCTGGACGCCTTC
ILP4Fwd87 AACCACCGAAGAACAACAGC
ILP4R1 GAGGGCCTGTAGATCACGAA
ILP5F1 CGGAGATGACGGACCTGTTC
ILP5Fwd343 AGCTCGTCTCACACATGAAC
RT-QPCR PRIMERS
ILP1Fwd131 AGGCAGAGTTCTACGATCCG
ILP1Rev210 GGACACCAGAGGAAACAGTC
ILP3Fwd108 CTTTTGAGGCTCTGCCAAGA
ILP3Rev201 CCCGTGCGCTTGTTGTTATC
ILP4Fwd87 AACCACCGAAGAACAACAGC
ILP4Rev189 GCCTCCACCAGGTCTACGAA
ILP5Fwd343 AGCTCGTCTCACACATGAAC
ILP5Rev452 CAGGAACAGGTCCGTCATCT
β-tubulinFwd TGAATGACCTGGTGTCCGAG
β-tubulinRev GACAAGCTGTTCAAGCCTCT