In vitro binding affinity towards Tat/TAR to determine interaction between TAR RNA and Tat peptide at room temperature using fluorescence spectrophotometer
In vitro binding affinity towards Tat/TAR to determine interaction between TAR RNA and Tat peptide at room temperature using fluorescence spectrophotometer; nb denotes no binding
In vitro binding affinity towards Tat/TAR to determine interaction between TAR RNA and Tat peptide at room temperature using fluorescence spectrophotometer; mb denotes multiple binding
Inhibition of HIV1 Tat-mediated LTR promoter transactivation in Tat/GFP plasmid expressed in Jurkat cells assessed as GFP gene expression by FACS analysis
PubChem BioAssay. An HIV-1 Tat-TAR Fluorescence Polarization (FP) Counter Screen to evaluate Inhibitors Targeting HIV-1 Vif-dependent Degradation of Human APOBEC3G. (Class of assay: confirmatory)
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 20 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 5 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 1.3 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 0.31 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 2.5 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 0.63 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 0.005 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control
Activation of Tat-mediated HIV1 transcription in HEK293- FlpIn-FM cells harboring LTR driven CBR reporter co-expressing CMV driven CBG reporter assessed as maximum LTR activity at 0.2 uM incubated for 48 hr using Chroma-Glo substrate by luciferase dual reporter cellular assay relative to control