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. 2011 Oct 18;143(1):107–121. doi: 10.1530/REP-11-0340

Table 2.

Antibodies used in this study.

Antigen Species Company (cat#) Dilution (IF; IB) Block (IB)
Actin, native G SCBT (Ac-1616) ND; 1:3000 NFDM
Cytokeratin 7, native M Invitrogen (18-00234) 1:300; 1:3000 NFDM
Cytokeratin 18, native M Invitrogen (18-0158Z) 1:100; 1:1000 NFDM
Cytokeratin 18, cleaved M Roche (12140322001) 1:100; 1:1000 NFDM
Caspase 8, cleaved Rb CST (9496) 1:100; 1:1000 BSA
E-cadherin, native Rb Abcam (ab40772) 1:300; 1:3000 NFDM
E-cadherin, native M Invitrogen (18-0223) 1:100; ND ND
hCG Rb Gift from Irv Boime 1:100; ND ND
Ki67 (MIB1) M Dako (M7240) 1:100; ND ND
PARP1, cleaved Rb CST (9541) 1:100; 1:1000 NFDM
Anti-rabbit, Alexa 488 G Invitrogen (A-21206) 1:200; NA NA
Anti-mouse, Alexa 555 G Invitrogen (A-11030) 1:200; NA NA

G, goat; M, mouse; Rb, rabbit; NA, not applicable; ND, not done; CST, Cell Signaling Technology; SCBT, Santa Cruz Biotechnology, Inc.; IF, immunofluorescence; IB, immunoblotting. Block, indicates if 5% BSA or 5% non-fat dry milk (NFDM) in 1× PBS was used for blocking before immunoblotting. For immunofluorescence, 5% BSA was used for blocking.