Wound healing assay cell type human

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Cellular assays Cell line authentication Human lung carcinoma cell line NCI-H1299

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCAEC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCtASMC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Get tips on using Human MesoEndo Cell Growth Medium to perform Mammalian cell culture media HCtAEC

Products Cell Applications Inc Human MesoEndo Cell Growth Medium

Human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) have been greatly used for studies on embryonic development and cell differentiation.iPSCs provide a stable source for either self-renewal or differentiation into suitable cells when cultured in a particular environment. Pluripotent cell culture was originally started by deriving cells from inner cell mass (ICM) from pre-implanted blastocysts, these were called embryonic stem cells. These cells after isolation can be grown on traditional extracellular matrices (like mouse embryonic fibroblasts, MEFs) or feeder-free culture systems. DMEM/F12 has been the most commonly used basal media in the culture of pluripotent cells. These cells are cultured at normal atmospheric oxygen levels, 21%, however, some studies have proposed that 4% oxygen tension may be better for hESC growth. Higher D-glucose concentration (4.2g/l) and osmolarity (320mOsm) that mimics the natural environment of embryonic tissue are optimal for the growth of hESCs. Supplements like N2 and/or B-27, in the presence of growth factors like bFGF, have been shown to increase pluripotency of these cells. bFGF, FGF2 and other ligands of receptor tyrosine kinases like IGF are also required or maintain self-renewal ability of these cells. TGFš›ƒ1, by its activation of SMAD2/3 signalling, also represses differentiation of iPSCs. Other compounds like ROCK inhibitors reduce blebbing and apoptosis in these cells to maintain their clonogenicity. However, an inhibitor for LIF (leukaemia inhibitory factor, which is one of the pluripotent genes) has an opposing effect. Therefore, it is important to understand the culture conditions and media composition that affect downstream signalling in hESCs or iPSCs that may lead to their differentiation.

Cell culture media Stem cell culture media Human bone mesenchymal stem cell (BMSC)

Get tips on using In Situ Cell Death Detection Kit, TMR red to perform TUNEL assay cell type - Rabbit synovial fibroblasts

Products Sigma-Aldrich In Situ Cell Death Detection Kit, TMR red

Get tips on using ApopTagĀ® Fluorescein In Situ Apoptosis Detection Kit to perform TUNEL assay cell type - A549, NCI-H460, H1299 human lung cancer cells

Products Millipore ApopTagĀ® Fluorescein In Situ Apoptosis Detection Kit

Get tips on using FragELā„¢ DNA Fragmentation Detection Kit, Colorimetric - TdT Enzyme to perform TUNEL assay cell type - A127, U87MG, U251MG, T98G human glioblastoma cells

Products Millipore FragELā„¢ DNA Fragmentation Detection Kit, Colorimetric - TdT Enzyme

Get tips on using In Situ Cell Death Detection Kit, Fluorescein to perform TUNEL assay cell type - Islets of langerhans (Beta cells)

Products Sigma-Aldrich In Situ Cell Death Detection Kit, Fluorescein

Get tips on using MagCellect Human B Cell Isolation Kit to perform Cell Isolation B cell

Products R&D Systems MagCellect Human B Cell Isolation Kit

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