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. 2007 Nov 2;190(2):546–554. doi: 10.1128/JB.00536-07

TABLE 2.

Primers used for PCR amplification

Primer Primer sequencea Purpose
CAT3 GGTTATACTAAAAGTCGTTTGTTGGTTC Primer extension
DTrev GCGAGCTCAACTTGTATGTGGTAACTTATGC R5+R6 deletions
lac5pX GCTCTAGACTGCATTGTTAAAATATGTATC EMSA
lac3pSc GCGAGCTCGTTTAAATTATAAACATAAAC EMSA
Protbio 5Bio-tctagaCAGTAGATGCTCATCTTTTTTTAG Affinity purification
R13pSc GCGAGCTCGAAAATATATCAATATTACCATTAAATTG R1 deletion
R23pSc GCGAGCTCATTTTATAATTTATATACAAAG R2 deletion
R33pSc GCGAGCTCAGAAATAAGATAATAGTAC R3 deletion
R43pSc GCGAGCTCGTTGAATAAAATTAAATAAG R4 deletion
R55pX GCTCTAGATATTCAACTTTGACAATTGAATAG R5 deletion
R65pX GCTCTAGACTTATTTCTAAATATTAACTC R6 deletion
rot3pSc GAGCTCGTGTAAATAAACTTGCTTTC EMSA
rot5pX CGGGATCCTTTGTTAATACTTGTATAG EMSA
rot5p2X TCTAGACAGTAGATGCTCATCTTTTTTTAG R1-R4 deletions
RotHis3pS GTCGACTTAGTGATGGTGATGGTGATGCACAGCAATAATTGCGTTTAAAC Construction of pHH3735
RotHis5pX TCTAGACAGTAGATGCTCATCTTTTTTTAGAACTTT Construction of pHH3735
Rotprom3p GCTAAACATCTCCCAATTAATAATC Affinity purification
a

Underlining signifies bases added to primers to create restriction endonuclease recognition sites.