Table 3

PCR primers Primers used in PCR for constructing deletions and for screening uvr alleles. All listed 5'→3'. Engineered restriction sites underlined

Primers for constructing deletions:
uvrA1 forward
GGGGGTACCGTATTTGTTCGGCACGAGGT
uvrA1 reverse
GGGTCTAGACTCTTCGCTCATTGGGAGAG


uvrA2 forward
GGGTCTAGACTCTCGCGGCTCTGTCTC
uvrA2 reverse
GGGAAGCTTACCGTCTCAGTGGTGGTGTC


uvrB1 forward
GGGGGTACCAGGAACGCGACCACTACG
uvrB1 reverse
GGGTCTAGAGCTGGCGTCACTCATTACAC


uvrB2 forward
GGGTCTAGAGAAACCGAGGACTGGTGAGA
uvrB2 reverse
GGGAAGCTTGGGAACACGAAGATGAGGAA


uvrC1 forward
GGGGGTACCGTACGTGGGTGTGATGAACG
uvrC1 reverse
GGGTCTAGATTCACGACTGTCTCCACGTC


uvrC2 forward
GGGTCTAGAAGAACGACGACTACGCGAAC
uvrC2 reverse
GGGAAGCTTACGTCTCGGAGTACCAGCAG


Primers for screening deletions by PCR
uvrA up
AATGTCGTAGTCGGCCATGT
uvrA down
CACAGCCCCGAGACAGAG


uvrB up
GGCCTACGACGAGTACACC
uvrB down
TGAAAAGCGTTGGTTTCTCC


ura3 up
CTTCCGGAGGACGTACAGG
ura3 down
CGTACTGGGCGTTCCACT


bla up
TTTGCCTTCCTGTTTTTGCT
bla down
TTGCCGGGAAGCTAGAGTAA

Crowley et al. Saline Systems 2006 2:11   doi:10.1186/1746-1448-2-11