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. 1998 Nov;180(21):5668–5675. doi: 10.1128/jb.180.21.5668-5675.1998

TABLE 2.

Plasmids used in this study

Plasmid Relevant characteristics Source or reference
pAD-GAL4 Activation domain cloning vector; AmprLEU2 Stratagene
pBD-GAL4 Binding domain cloning vector; CmrTRP1 Stratagene
p53 Murine p53-binding domain fusion; AmprTRP1 Stratagene
pSV40 Simian virus 40 large-T-antigen–activation domain fusion; AmprLEU2 Stratagene
pLaminC Human lamin C-binding domain fusion; AmprTRP1 Stratagene
pBD-Z1 FrzZ first domain-binding domain fusion; CmrTRP1 This study
pBD-Z2 FrzZ second domain-binding domain fusion; CmrTRP1 This study
pBD-E FrzE-binding domain fusion; CmrTRP1 This study
pBD-AsgA AsgA-binding domain fusion; CmrTRP1 Lynda Plamann, University of Missouri
pADLIB Library of random fragments from M. xanthus DZF1-activation domain fusions; AmprLEU2 This study
pAD-RpoE1 RpoE1-activation domain fusion; AmprLEU2 This study
pUC18 General cloning vector; Ampr 26
pZErO-2 Zero Background cloning vector; Kmr Invitrogen
pZRpoE1 Internal fragment of rpoE1 cloned in pZErO-2; Kmr This study
pZOrf5 Internal fragment of orf5 cloned in pZErO-2; Kmr This study
pBS9 6,464-bp fragment containing the 3′ end of frzZ and downstream genes cloned in pBlueScript This study