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. 2015 Dec 23;291(8):4256–4265. doi: 10.1074/jbc.M115.688762

TABLE 1.

Sequences of primers used for mutagenesis and qPCR

Usage Gene Forward primer Reverse primer
Mutagenesis Tet2 H1302Y GCTCATTCCTACAGAGACCAGCAGAACATGC GCATGTTCTGCTGGTCTCTGTAGGAATGAGC
Mutagenesis Tet2 D1304A GCTCAATTCCCACAGAGCCCAGCAGAACATGC GCATGTTCTGCTGGGCTCTGTGGGAATGAGC
Mutagenesis Tet2 H1802R GCAAAGTGTGAGGTTCGTGCCACAACC GGTTGTGGCACGAACCTCACACTTTGC
Mutagenesis Tet2 R1817M CCCCACCATGATCTCACTTGTACTGTATAGG CCTATACAGTACAAGTGAGATCATGGTGGGG
Mutagenesis Tet2 R1817S CCCCACCAGTATCTCACTTGTACTGTATAGG CCTATACAGTACAAGTGAGATACTGGTGGGG
qPCR TBP GAATATAATCCCAAGCGGTTT ACTTCACATCACAGCTCCCC
qPCR TET1 GAGAATAGGTATGGTCAAAA CTTCATCACTGCTTCTTCTT
qPCR TET2 TGCCGTCTGGGTCTGAAG CCTCAGGTTTTCCTCCAAAT
qPCR TET3 CGTCGAACAAATAGTGGAGA CTTTCCCCTTCTCTCCATAC
qPCR VEGFA AGGAGGAGGGCAGAATCATCA ATGTCCACCAGGGTCTCGATTG
qPCR BNIP3 CCACCTCGCTCGCAGACACCAC GAGAGCAGCAGAGATGGAAGGAAAAC
qPCR PGK1 CTGTGGGGGTATTTGAATGG CTTCCAGGAGCTCCAAACTG
qPCR HK2 ATTGTCCAGTGCATCGCGGA AGGTCAAACTCCTCTCGCCG
qPCR ENO1 TGGTGTCTATCGAAGATCCCTT CCTTGGCGATCCTCTTTGG
qPCR IDH1 TGTGGTAGAGATGCAAGGAGA TTGGTGACTTGGTCGTTGGTG