PubMed
Harbison CT et al., Nature, 2004 Sep 2;431(7004):99-104Harbison CT et al., Nature, 2004 Sep 2;431(7004):99-104
Direct
Chip-on-chip
N/A
S288c
N/A
PubMed
Wang Z et al., J Biol Chem, 2009 Jan 9;284(2):839-47Wang Z et al., J Biol Chem, 2009 Jan 9;284(2):839-47
Indirect
RT-PCR - wt vs TF mutant
Positive
S288c
cells were grown to mid-exponential phase in SD medium supplemented with 0.8 mm ?-aminolevulinic acid (ALA)
PubMed
Bergenholm D et al., mSystems, 2018 Jul-Aug;3(4):Bergenholm D et al., mSystems, 2018 Jul-Aug;3(4):
Direct
ChIP-exo
N/A
CEN.PK 113-5D
Steady state aerobic chemostat cultivation at 30 .C in glucose-limited minimal medium containing vitamins and trace metals and maintained at pH 5.0
Direct
ChIP-exo
N/A
CEN.PK 113-5D
Steady state chemostat cultivation at 30 .C in oxygen- and glucose-limited minimal medium containing vitamins and trace metals and maintained at pH 5.0
PubMed
Holland P et al., Nucleic Acids Res, 2019 Jun 4;47(10):4986-5000Holland P et al., Nucleic Acids Res, 2019 Jun 4;47(10):4986-5000
Direct
ChIP-exo
N/A
CEN.PK 113-5D
Cells were cultivated in chemostats in anaerobic glucose limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
Direct
ChIP-exo
N/A
CEN.PK 113-5D
Cells were cultivated in chemostats in nitrogen limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
Direct
ChIP-exo
N/A
CEN.PK 113-5D
Cells were cultivated in chemostats in respiratory glucose limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h