Get tips on using Senescence Cells Histochemical Staining Kit to perform Reporter gene assay β-galactosidase substrates - mouse embryonic fibroblasts
A gross majority of classical apoptotic attributes can be quantitatively examined by flow cytometry, the preferred platform for rapid assessment of multiple cellular attributes at a single-cell level. However, sample preparation for such flow cytometry-based techniques could be challenging. Cell harvesting by trypsinization, mechanical or enzymatic cell disaggregation from tissues, extensive centrifugation steps, may all lead to preferential loss of apoptotic cells. To overcome this strictly follow manufacturers instruction of the detection kit.
Get tips on using Endothelial Cell Medium to perform Mammalian cell culture media CADMEC/HMVEC
Get tips on using Vascular Cell Basal Medium to perform Mammalian cell culture media HCAEC
Get tips on using Smooth Muscle Cell Medium to perform Mammalian cell culture media HAOSMC
Get tips on using Canine Endothelial Cell Media to perform Mammalian cell culture media CnAOEC
Get tips on using Bovine Endothelial Cell Media to perform Mammalian cell culture media BAOEC
Get tips on using KAPA LongRange to perform PCR Hot start PCR - Mammalian DNA
Get tips on using PCR SuperMix to perform PCR Conventional / Qualitative PCR - mammalian DNA
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
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