A, schematic representation of serial p21waf1 / cip1 promoter — driven
luciferase reporters used in transactivation assay: p21 - Luc contains the 2.3 - kb full - length of p21waf1 / cip1 promoter (from − 2,326 to +10 nucleotide related transcription start site); its derivatives (− 159 / +8) p21 - Luc, (− 123 / +8) p21 - Luc, (− 84 / +8) p21 - Luc, (− 76 / +8) p21 - Luc, (− 63 / +8) p21 - Luc, and (− 56 / +8) p21 - Luc contain a series of deleted promoters of p21waf1 / cip1.
Not exact matches
After 24 hours,
luciferase activities were measured by
using dual -
luciferase reporter assay system (Promega).
Ten nanograms of
reporter plasmid and 200 ng of miR7 expression plasmid were cotransfected with 1 ng of phRG - TK Renilla
luciferase internal control plasmid (Promega) into 293TN cells
using Lipofectamine 2000 reagent (Invitrogen).
To more fully explore the effects of compound on Bach1 activity, a
luciferase reporter assay
using the HMOX1 E2 ARE as a target was developed.
The clone, pGL - MARE - Luc, was confirmed via DNA sequencing before being
used in the
luciferase reporter assay.
Luciferase activities were measured
using the Dual -
Luciferase Reporter Assay kit (Promega) following the manufacturer's instructions.
The cells were cotransfected with the
reporter gene constructs and related expression plasmids as indicated by
using SuperFect (Qiagen) followed by transcriptional activity assay
using Dual -
Luciferase Assay System (Promega) according to the manufacturer's instruction.
The Dual -
Luciferase Reporter Assay System (E1910; Promega, Madison, WI) was used to perform dual - reporter assays on NFκB luciferase and Renilla luciferase (internal
Luciferase Reporter Assay System (E1910; Promega, Madison, WI) was used to perform dual - reporter assays on NFκB luciferase and Renilla luciferase (internal c
Reporter Assay System (E1910; Promega, Madison, WI) was
used to perform dual -
reporter assays on NFκB luciferase and Renilla luciferase (internal c
reporter assays on NFκB
luciferase and Renilla luciferase (internal
luciferase and Renilla
luciferase (internal
luciferase (internal control).
For DNA transfection, the HepG2, 293, and 293T cells were seeded respectively at 2 × 105, 2 × 105, and 1 × 105 cells / well in 24 - well plates overnight, and then the p53 - TA - Luc
luciferase reporter plasmid and RSV - lacZ plasmids were transiently transfected into the cells
using NTRII for 6 h, followed by treatment with the test compounds.
The researchers took a FRET
reporter and adapted it into a BRET
reporter by
using NanoLuc ®
Luciferase to excite the Venus fluorescent protein in conjunction with a membrane - inserted voltage sensing domain (LOTUS V; Luminescent Optical Tool for Universal Sensing of Voltage).
Gene expression
Reporter genes, such as
luciferase or GFP, can also be assessed in microplate readers, enabling in vitro and in vivo determination of gene expression for studies
using markers of genetic alteration.
Luciferase activities were measured using the Dual - Luciferase Reporter Assay System (Promega) and normalized to Renilla luciferase
Luciferase activities were measured
using the Dual -
Luciferase Reporter Assay System (Promega) and normalized to Renilla luciferase
Luciferase Reporter Assay System (Promega) and normalized to Renilla
luciferaseluciferase activity.