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TABLE 2.

Oligonucleotides used for gel shift assays

Gene SOS box label Sequence of oligonucleotidea
recA recA0 tgaatcGAACaggtGTTCggctac
lexA lexA1a cctgtcGAACacatGTTtgattct
lexA1b atatccGAACatttGaTCgaagcg
lexA2a cggttgGAgCcggacTTCcggcgc
lexA2b gtaatcGctCgcgtGTTCgacact
ruvA ruvA0 gctatcGAACgggtGTTCtctcag
ruvC ruvC0 cgtatcGAACgattGTTCggaaat
ruvC2a atttaccAtCgcacGTTCcatagg
ruvC2b gtgtgcGAtCgagcGTTtcccgaa
ssb ssb2a gaactcGAcCgccaGcTCagcctc
ssb2b ccatacGAAatcatGgTCatcctc
dnaB dnaB1 gttgtcGAAtatgcGTTCgggtgc
recN recN2a cggctgGtgCgcaaGTTCcggttg
recN2b catcgtcAACcgggGTTgggcgct
dinP dinP2a ccgctgGAcCgcctGaTCgcattc
dinP2b gcaaagGcACcttgtTTCgccgct
recC recC1 gaagccGcACgagaGTTCgccggt
recC2a cgacaaGAAggcccGTaCcgactg
recC2b gggataGcAgccgaGTTCgggctg
a

In each case, the complementary oligonucleotide was annealed with the sequence given and the resulting double-stranded probe was used in the gel shift; the bases matching the consensus SOS box sequence are shown in uppercase.