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. 2009 Nov 13;192(2):599–603. doi: 10.1128/JB.01066-09

TABLE 2.

Primers

Primer Sequencea Use
sigA f TCGGTTCGCGCCTACCT TaqMan primer
sigA p TTGAGCAGCGCTACCTTGCCG TaqMan probe
sigA r TGGCTAGCTCGACCTCCTCCT TaqMan primer
ruvC f GCTCAGGTCACCGCGATG TaqMan primer
ruvC p CACCAAAATCCTTGCGCTGCAAGCT TaqMan probe
ruvC r CGGCCGGTGTCGGTT TaqMan primer
ruvC small f AATCTAGAGGTCGGGGCCGGCTCAATCTC Cloning
ruvC small r CGAAGCTTAGCTGCCGACCACGCCCACTCT Cloning and primer extension
ruvC 1f CTAGGTGTCCTGCGCGGGATGTCGGGACGATCCGCTAGCGTATCGAACGATTGTTCGGAAATGG Cloning
ruvC 1r AGCTCCATTTCCGAACAATCGTTCGATACGCTAGCGGATCGTCCCGACATCCCGCGCAGGACAC Cloning
ruvC 3f CTAGGTGTCCTGCGCGGGATGTCGGGACGATCCGCTAGCGTATCGAACGA Cloning
ruvC 3r AGCTTCGTTCGATACGCTAGCGGATCGTCCCGACATCCCGCGCAGGACAC Cloning
ruvC 7f CTAGGTGTCCTGCGCGGGATGTCGGGACGATCCGCTCGCGTATCGAACGATTGTTCGGAAATGG Cloning
ruvC 7r AGCTCCATTTCCGAACAATCGTTCGATACGCGAGCGGATCGTCCCGACATCCCGCGCAGGACAC Cloning
ruvC 8f CTAGGTGTCCTGCGCGGGATGTCGGGACGATCCGCTAGCGTATCGAACGATTGTTCAGAAATGG Cloning
ruvC 8r AGCTCCATTTCTGAACAATCGTTCGATACGCTAGCGGATCGTCCCGACATCCCGCGCAGGACAC Cloning
a

The underlined bases indicate bases added to the native sequence to form overhangs compatible with restriction sites on annealing of appropriate pairs of oligonucleotides.