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. 2004 Dec;15(12):5443–5455. doi: 10.1091/mbc.E04-07-0608

Table 2.

Plasmids used in this study

Name Abbreviation Description Source
pRS316 RAD53 3×FLAG pRAD53 F RAD53 3 × FLAG under endogenous Rad53 promoter Our laboratory
pRS316 rad53 kDa 3×FLAG prad53 kDa F rad53 kDa 3 × FLAG under endogenous Rad53 promoter Our laboratory
pRS315 RAD53 2 ×HA pRAD53 H RAD53 2 × HA under endogenous Rad53 promoter Our laboratory
pRS305 DUN1 13×MYC DUN1 13 × MYC genomic integration plasmid Cut Nco I to target Our laboratory
pRS315 MYC-MEC1 pMEC1 18 × MYC MEC1 under endogenous Mec1 promoter Our laboratory
pRS316 DDC2-RAD53 3× FLAG pD2-R53 F DDC2 ORF fused with RAD53 3 × FLAG at the 5′end of RAD53 under Rad53 promoter Our laboratory
pRS316 DDC2-rad53 kDa 3× FLAG pD2-r53 kDa F DDC2 ORF fused with rad53 kDa 3 × FLAG at the 5′end of RAD53 under Rad53 promoter Our laboratory
pRS315 DDC2-RAD53 2 × HA pD2-R53 H DDC2 ORF fused with RAD53 2 × HA at the 5′end of RAD53 under Rad53 promoter Our laboratory
pRS306 DDC2-RAD53 DDC2-RAD53 genomic integration plasmid Cut SexA I to target Our laboratory
pRS316 DDC2 3× FLAG pD2 F DDC2 ORF 3 × FLAG under endogenous Rad53 promoter and Rad53 3′UTR Our laboratory
pRS316 DDC2-3× HA pD2 H DDC2 ORF 3 × HA under endogenous DDC2 promoter and ADH1 terminator Our laboratory
pRS305 DDC2-3 × FLAG DDC2 genomic integration plasmid Cut Ndel to target Our laboratory
pRS316 ddc2KA 3× FLAG pd2KA F ddc2KA(ddc2 K177A, K178A) 3 × FLAG under endogenous Rad53 promoter and Rad53 3′UTR Our laboratory
pGEX 4T2 DDC2 pGST-DDC2 Bacterial expression vector for GST-Ddc2 Our laboratory