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. 1998 Nov;180(21):5697–5703. doi: 10.1128/jb.180.21.5697-5703.1998

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
pBDZ1 FrzZ first domain-binding domain fusion; CmrTRP1 This study
pBDZ2 FrzZ second domain-binding domain fusion; CmrTRP1 This study
pBDE FrzE-binding domain fusion; CmrTRP1 This study
pBD-AsgA AsgA-binding domain fusion; CmrTRP1 Lynda Plamann, Univer-sity of Missouri
pADLIB Library of random fragments from M. xanthus DZF1-activation domain fusions; AmprLEU2 This study
pADZ165a C-terminal AbcA-activation domain fusion; AmprLEU2 This study
pUC18 General cloning vector; Ampr 41
pZErO-2 Zero Background cloning vector; Kmr Invitrogen
pZABC Internal fragment of abcA cloned in pZErO-2; Kmr This study
pZORF3 Internal fragment of orf3 cloned in pZErO-2; Kmr This study
pZCTR Internal fragment of ctrA cloned in pZErO-2; Kmr This study
pABCS3.5 3.5-kb SacI fragment of abc operon cloned in pUC18; Ampr This study
pABCS1.8 1.8-kb SacI fragment of abc operon cloned in pUC18; Ampr This study
pABCS1.3 1.3-kb SacI fragment of abc operon cloned in pUC18; Ampr This study
pABCBK2.1 2.1-kb BamHI-KpnI fragment of abc operon cloned in pUC18; Ampr This study