Flow cytometry protocol for thp-1 cell
WebCell cycle assay protocols for flow cytometry. Vybrant DyeCycle Violet Stain. Vybrant DyeCycle Green and Orange Stains. Vybrant DyeCycle Ruby Stain. FxCycle Violet … WebWith the same method, the IL-1β in THP-1 cells stimulated with 10 ng/mL of S. enteritidis LPS was 34.8%, whereas after selonsertib administration it was detected at 2.0% using …
Flow cytometry protocol for thp-1 cell
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WebSep 25, 2009 · THP-1 cell surface markers for Flow Cytometry - Need a robust marker for undifferentiated THP-1 cells. I am working with THP-1 cells (ATCC TIB 202), a human monocytic cell line. The majority of people that use this cell line are interested in the differentiated macrophage phenotype, which can be achieved by stimulating THP-1 cells … Web1 day ago · An increase in exposure of β-(1,3)-glucan and chitin on the cell surface was also observed through flow cytometry. Interestingly, we observed a decrease in the phagocytosis rate when the Δcdc50 mutant was co-incubated with THP-1 macrophages. The Δcdc50 mutant also exhibited weakened virulence in nematode survival tests.
WebMar 11, 2024 · We describe and validate a flow cytometry-based protocol for quantifying G4 levels by using the G4-specific antibody BG4 to label standard cultured cells (Hela and THP-1) as well as primary cells obtained from human blood (peripheral blood mononuclear cells (PBMCs)). We additionally determined changes in G4 levels during the cell cycle in ... WebFeb 3, 2024 · Single-cell preparation from different organs, staining of cells with fluorophore-conjugated antibodies, and analysis of the stained cells using flow …
WebProtocol for high-throughput compound screening using flow cytometry in THP-1 cells. Flow cytometry is a valuable method for analyzing protein expressions at the single cell level but can be ... WebCommon cell preparation technique and staining protocols for surface and trapped markers to help get the best quality flow cytometry data. Locate out more. Standard per preparation techniques and coloring protocols for emerge press intracellular markers to assist get the best quality run cytometry data. Find out more
WebApr 14, 2024 · A similar approach has been used to characterize the adherence and transmigration properties of peripheral blood mononuclear cells on human aortic endothelial cells and brain microvascular endothelial cells . One limitation of the flow cytometry-based assay was the inherent variability in the cells used; for example, the passage number of …
Web5 Collect 2 million cytotoxic T cells per sample (i.e. per well) from an on-going culture 6 Spin them down at 350 x gfor 00:05:00 at 4 °C and re-suspend them in fresh media at 1 million per mL concentration 7 Supplement T cells with 200 IU/mL rIL2 8 Aspirate the culture media from each of the 24-well-plate wells that contain a sample. Try to aspirate as much as … increased by a factor of 10WebJun 1, 2024 · This protocol provides instructions to perform a high-throughput small molecule screen using flow cytometry analysis of THP-1 cells, a human monocytic leukemia cell line. We describe a … increased by a factor of 4WebPublished protocols using the promonocytic cell line THP-1 have tended to result in cells that closely resemble classically-activated macrophages, differentiated in IFNγ and LPS. … increased by cpiWebFor the detection of the viability of Jurkat and THP-1 cells, an MTT assay was employed as previously described . Briefly, both Jurkat and THP-1 cells in the logarithmic growth phase were seeded at a density of 1 × 10 5 cells/well on a 24-well plate and treated with various concentrations (40, 20, 10, 5 and 2.5 µM) of each compound. After the ... increased by an order of magnitudeincreased by the product of a numberWebJan 13, 2010 · We have compared the phenotype of the promonocytic THP-1 cell line after various protocols of differentiation utilising VD3 and PMA in comparison to primary human monocytes or monocyte-derived macrophages (MDM). ... Flow cytometry was performed to estimate the number of latex beads ingested per cell with each peak assumed to equal … increased by factor of 3WebIntracellular Staining Flow Cytometry Output Using Detergents to Permeabilize Mobile; Centrifuge cells as by Step 3 and resuspend include appropriate volume in Flow Cytometry Coloring Buffer press buffer of choice so that the final cellular concentration is 1 x 10 7 cells/mL (other cell concentrations may been reasonably for different experiments) increased by a factor meaning