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. Author manuscript; available in PMC: 2007 Feb 17.
Published in final edited form as: J Biol Chem. 2005 Dec 14;281(7):3899–3908. doi: 10.1074/jbc.M511761200

TABLE 1.

Primers used for this study

Primer name Sequencea(5′→3direction) Comments
AccA3F GGCATATGGCTAGTCACGCCGGCT Upstream of accA3, NdeI site added
AccA3R GGAGATCTTTACTTGATCTCGGCG Downstream of accA3, BglII site added
AccD4F GGCATATGACCGTCACCGAGCCG Upstream of accD4, NdeI site added
AccD4R GGCTCGAGTCAGGCCGTGCTTGC Downstream of accD4, XhoI site added
AccD5F GGCATATGACAAGCGTTACCGAC Upstream of accD5, NdeI site added
AccD5R GGCTCGAGTCACAGGGGCACGTT Downstream of accD5, XhoI site added
1ENF CATATGGGAACGTGCCCCTGTG Upstream 1M of Rv3281, NdeI site added
1ECR GGATCCTCGGCGCATGTGCGTC Downstream of Rv3281, BamHI site added
102EF GGCATATGACCGAGAAGCCGCTGC Positions 102V of Rv3281, NdeI site added
102ER GCTCGAGTCATCGGCGCATGTGCGTC Downstream of Rv3281, XhoI site added
D5–227F CTTCGTGTACCGCCAGCAGCTGG Internal primer of accD5, RT-PCR
E-139R CTGCCGGATTGTTCGTCTCGTTC Internal primer of Rv3281, RT-PCR
a

Endonuclease restriction sites added to sequences are underlined.