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. 2004 Apr;15(4):1904–1917. doi: 10.1091/mbc.E04-01-0004

Table 2.

Plasmids used in this study

Plasmid Contents Source
BSE 19 pRS315 Sikorski and Hieter (1989)
BSE 119 pRS425 Christianson et al. (1992)
BSE 345 PXL1 gene in pRS315: −1000/+500, LEU-based plasmid, cloned Xho1-Sac1
BSE 346 PXL1 gene in 2 micron vector pRS425; −1000/+500, LEU-based plasmid, cloned Xho1-Sac1
BSE 352 pRS315 containing GFP::PXL1 and −1000 bp of upstream and +500 bp of downstream PXL1
BSE 364 GFP-pxl1-LIM only clone, constructed by removing PXL1 coding sequences for a.a. 1-502 from BSE352
BSE 365 GFP-pxl1-N terminus clone, constructed by inserting a nonsense codon into PXL1 in BSE352
BSE 378 pxl1-lim1; PXL1-H581l/C584A site-directed mutagenesis clone of LIM domain 1 substituted in BSE345
BSE 379 pxl1-lim2; PXL1-H642l/C645A site-directed mutagenesis clone of LIM domain 2 substituted in BSE345
BSE 385 GFP-Pxl1-H581l/C584A site-directed mutagenesis clone substituted in BSE352
BSE 386 GFP-Pxl1-H642l/C645A site-directed mutagenesis clone substituted in BSE352

All plasmids were constructed for this study unless otherwise indicated.