DNA transfection Mammalian cells

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RNA siRNA / miRNA gene silencing Rat Retinal stem cells Brn-3b

Cell culture media 3D Cell Culture Media Human primary breast ephitelial cells-organoids

Cell culture media 3D Cell Culture Media Human primary breast ephitelial cells-Mammospheres

Cell culture media 3D Cell Culture Media Mouse primary mammary ephitelial cells- organoids

Cell culture media 3D Cell Culture Media Mouse primary lung epithelial cells-organoids

Cell culture media 3D Cell Culture Media Mouse primary breast ephitelial cells-Mammospheres

Cellular assays Cell line authentication Human iPSC cells derived from human dermal fibroblasts

Get tips on using RPMI-1640 with Phenol Red produced by FUJIFILM Wako Pure Chemical Corporation to perform Mammalian cell culture media Ku812

Products Alpha laboratories RPMI-1640 with Phenol Red produced by FUJIFILM Wako Pure Chemical Corporation

Reporter gene assays are designed to test the regulation of the expression of a gene of interest. This is usually done by linking the promoter of the gene of interest with a gene such as a firefly luciferase, which can be easily detected by addition of luciferin that leads to an enzymatic reaction to produce luminescence. The enzymatic reaction can be correlated to the expression of the gene of interest. Another luciferase gene that can be used is Renilla luciferase. For an appropriate luciferase assay: 1. the reporter should express uniformly in all cells, 2. specifically respond to effectors that the assay intends to monitor, 3. have low intrinsic stability to quickly reflect transcriptional dynamics. It is important to have an equal number of cells plated in each testing condition to avoid any incorrect readouts. Reporter assays could be single or dual reporter assays. The reporter could be both luciferases. Most dual-luciferase assays involve adding two reagents to each sample and measuring luminescence following each addition. Adding the first reagent activates the first luciferase reporter reaction; adding the second reagent extinguishes first luciferase reporter activity and initiates the second luciferase reaction. Dual-luciferase assays have some advantages, including 1. reduces variability, 2. reduces background, 3. normalizes differences in transfection efficiencies between samples.

Cellular assays Reporter gene assay β-galactosidase substrates SK-Hep-1

RNA siRNA / miRNA gene silencing Rat Brain endothelial cells HIF-1α Lipid

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