PubChem BioAssay. A quantitative high throughput screen for small molecules that induce DNA re-replication in MCF 10a normal breast cells. (Class of assay: confirmatory)
PUBCHEM_BIOASSAY: qHTS Inhibitors of AmpC Beta-Lactamase (assay with detergent). (Class of assay: confirmatory) [Related pubchem assays: 1002 (Confirmation Concentration-Response Assay for Inhibitors of AmpC Beta-Lactamase (assay with detergent)), 585 (Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay without detergent) - a screen old NIH MLSMR collection), 584 (Promiscuous and Specific Inhibitors of AmpC Beta-Lactamase (assay with detergent) - a screen of the old NIH MLSMR collection), 1003 (Confirmation Cuvette-Based Assay for Inhibitors of AmpC Beta-Lactamase (assay with detergent))]
Positive allosteric modulation of recombinant human glycine receptor alpha3 expressed in CHOK1 cells at -60 mV holding potential by whole cell patch-clamp method
Positive allosteric modulation of recombinant human glycine receptor alpha3 expressed in CHOK1 cells assessed as potentiation of glycine-induced current at 20 uM at -60 mV holding potential by whole cell patch-clamp method relative to glycine
Positive allosteric modulation of recombinant human glycine receptor alpha1 expressed in CHOK1 cells assessed as potentiation of glycine-induced current at 10 uM at -60 mV holding potential by whole cell patch-clamp method relative to glycine
Positive allosteric modulation of recombinant human GABAA receptor alpha1beta3gamma2 expressed in CHOK1 cells assessed as potentiation of GABA-induced current at 10 uM at -60 mV holding potential by whole cell patch-clamp method relative to GABA
Positive allosteric modulation of recombinant human GABAA receptor alpha2beta3gamma2 expressed in CHOK1 cells assessed as potentiation of GABA-induced current at 10 uM at -60 mV holding potential by whole cell patch-clamp method relative to GABA