Site Directed Mutagenesis (SDM) Human Insertion HepG2

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Reporter gene assays enable high sensitivity measurement of gene expression and cell signaling through the addition of bioluminescent genes into target cells. One of the major challenges is to make a specific construct that has no responses other than those related to the signaling pathway of interest. This can be achieved by selecting highly specific reporter constructs containing only defined responsive elements and a minimal promoter linked to reporter enzymes such as luciferase

Cellular assays Reporter gene assay β-galactosidase substrates HepG2

Cellular assays Cell line authentication Liver carcinoma cell line HepG2

Reporter gene assays enable high sensitivity measurement of gene expression and cell signaling through the addition of bioluminescent genes into target cells. One of the major challenges is to make a specific construct that has no responses other than those related to the signaling pathway of interest. This can be achieved by selecting highly specific reporter constructs containing only defined responsive elements and a minimal promoter linked to reporter enzymes such as luciferase

Cellular assays Reporter gene assay luciferase HepG2 and Huh7 cells

Transfection is a powerful technique that enables the study of the function of genes and gene products in cells. Based on the nature of experiments, we may need a stable DNA transfection in cells for persistent gain-of-function or loss-of-function of the target gene. For stable transfection, integration of a DNA vector into the chromosome is crucial which requires selective screening and clonal isolation. By carefully selecting a viral delivery system and related reagents we can ensure safe and highly-efficient delivery of expression constructs for high-level constitutive or inducible expression in any mammalian cell type.

DNA DNA transfection Mammalian cells Immortalized cell lines HepG2

The estimation of DNA methylation level heavily depends on the complete conversion of non-methylated DNA cytosines. It is crucial to ensure complete conversion of non-methylated cytosines in DNA. Therefore, it is important to incorporate controls for bisulfite reactions, as well as to pay attention to the appearance of cytosines in non-CpG sites after sequencing, which is an indicator of incomplete conversion.

DNA DNA methylation profiling Gene specific profiling HepG2 Constitutive Androstane Receptor (CAR)

Get tips on using Human Genome CGH Microarray Kit 244A to perform Microarray Comperative genomic hybridization - Human HepG2

Products Agilent Technologies Human Genome CGH Microarray Kit 244A

Get tips on using Accell Human VDAC1 (7416) siRNA - Set of 4 to perform siRNA / miRNA gene silencing Human - HepG2 VADC1

Products Dharmacon Accell Human VDAC1 (7416) siRNA - Set of 4

Get tips on using Imprint® Chromatin Immunoprecipitation Kit to perform ChIP Human - HepG2

Products Sigma-Aldrich Imprint® Chromatin Immunoprecipitation Kit

Get tips on using Silencer select_FGA siRNA to perform siRNA / miRNA gene silencing Human - HepG2 FGA

Products Thermo Fisher Scientific Silencer select_FGA siRNA

Get tips on using Silencer select_FGB siRNA to perform siRNA / miRNA gene silencing Human - HepG2 FGB

Products Thermo Fisher Scientific Silencer select_FGB siRNA

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