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. 2012 Oct 3;287(48):40119–40130. doi: 10.1074/jbc.M112.418889

TABLE 1.

PCR primers used in this study

ISCU exon 2–4 DNA probe template Forward AAAATCCTAGAAACGTGGGG
ISCU exon 2–4 DNA probe template Reverse TGCAGTTTCACGGGAGGAAG
ISCU exon 4A–intron 4 DNA probe template Forward TCCAGCAGAGGAGAAAACTCAGC
ISCU exon 4A–intron 4 DNA probe template Reverse CCAGGCTTCCTGAAGAATGAGTT
ISCU exon 5 DNA probe template Forward CTGGCTGAAGATGCAATCAA
ISCU exon 5 DNA probe template Reverse CAGACCAAGGCATTCTACTG
ISCU exon 2–4 T7 RNA probe template Forward AAAATCCTAGAAACGTGGGG
ISCU exon 2–4 T7 RNA probe template Reverse TAATACGACTCACTATAGGGAGATGCAGTTTCACGGGAGGA
ISCU exon 4A–intron 4 T7 RNA probe template Forward AATCTGTGCTGTTTCCAGC
ISCU exon 4A–intron 4 T7 RNA probe template Reverse TAATACGACTCACTATAGGGAGACCAGGCTTCCTGAAGAATGAGTT
ISCU exon 2–3 qPCR primer Forward GGCTCCAGCATGTGGTGACGTA
ISCU exon 2–3 qPCR primer Reverse GCGGAACCACAGCCAAATGT
ISCU exon 4A qPCR primer Forward TCCAGCAGAGGAGAAAACTCAGC
ISCU exon 4A qPCR primer Reverse CCGACAGGAATACCATCCAGACA
ISCU exon 5 qPCR primer Forward AGCAGGCCACACCAGCTGTT
ISCU exon 5 qPCR primer Reverse GGAAGCGGCTTCTGAACATCTA
ISCU intron 4 qPCR primer Forward TAAGTCCCCACACTATCCTGGC
ISCU intron 4 qPCR primer Reverse GTTCCTTAGCCTCTTTGACCCT
MYOD1 qPCR primer Forward CGACGGCATGATGGACTACA
MYOD1 qPCR primer Reverse TGGGCGCCTCGTTGTAGTAG
MYH1 qPCR primer Forward CTAAAACTCCTGGTGCCATGGA
MYH1 qPCR primer Reverse TTCCTGCAGATGCGGATGC
ISCU1 ORF cloning primer Forward TTAAGCTTCCACCATGGTTCTCATTGACATGAGTG
ISCU2 ORF cloning primer Forward ATTAAGCTTCCACCATGGCGGCGGCTGGGGCTTTC
ISCU universal ORF cloning and Myc tagging primer Reverse CGCCTCGAGCTACAGATCTTCTTCAGAAATAAGTTTTTGTTCTTTCTTCTCTGCCTCTCCTTTTTTGGG