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. 2008 Nov 24;29(3):714–725. doi: 10.1128/MCB.00825-08

TABLE 1.

Primers used for cloning

Primer Orientationa Sequenceb Description
pCMVmyc-SUMO1 F ATCCCC[AAGCTT]ATGTCTGACCAGGAGGCA HindIII
R ATTCGC[GGATCC][CTA]ACCCCCCGTTTGTTCCTG BamHI; stop codon
pCMVmyc-SUMO2 F AATCCG[GAATTC]ATGGCCGACGAAAAGCCCAA EcoRI
R TAACGC[GGATCC][TCA]ACCTCCCGTCTGCTGTTGG BamHI; stop codon
pCMVmyc-SUMO3 F AATCCG[GAATTC]ATGTCCGAGGAGAAGCCC EcoRI
R AATCGC[GGATCC][CTA]ACCTCCCGTCTGCTGCTG BamHI
pCMV myc-Ufm1 F CACCCG[GAATTC]ATGTCGAAGGTTTCCTTTAAG EcoRI
R ATTCGC[GGATCC]TTAACAACTTCCAACACGATC BamHI
pGEX4T-1 N-CTCF (amino acids 1-266) F TACCG[GAATTC]ATGGAAGGTGAGGCGGTTG EcoRI
R TATCCG[CTCGAG]CTGGAATGTTTTCTTTACACC XhoI
pGEX4T-1 C-CTCF (amino acids 570-736) F TTACGC[GGATCC]ATGGCAAGACATGCAGATAACTG BamHI
R TATCCG[CTCGAG]TCACCGGTCCATCATGCTGAG XhoI
a

F, forward; R, reverse.

b

Brackets indicate restriction enzyme sites and stop codons engineered into the primers.