WebAdd the appropriate amount of labeled primary antibody. If the primary antibody needs to be diluted use Cell Staining Buffer as the diluent. Incubate for 15 – 60 minutes on ice in the dark. Incubation times should also be optimized. Fill tube fill Cell Staining buffer, centrifuge at 250 x g for five min., discard supernatant, and repeat. WebOct 21, 2024 · Cells in stain buffer: 110 μL: Total volume: 200 μL: Note: Antibody cocktail volumes can be scaled up based on the number of samples or amount of cells. Optional: when two or more BD Horizon™ Brilliant dyes are present in the sorting panel, Brilliant Stain Buffer (BSB) Plus should be used to mitigate dye to dye interaction and staining ...
Cell Press: STAR Protocols
WebNov 9, 2024 · Stain cultured cells with phalloidin conjugates. Tip: Pre-incubating fixed cells with 1% BSA in PBS for 20–30 minutes may improve staining. Tip: When staining coverslips, keep them in a covered … WebFollowing washing, cells should be resuspended at 1 -2 x 10 6 cells/mL, whether for ICC staining in solution, or smear application for subsequent staining on slides specially treated to enhanced adhesion of cells. When adherent cells are cultured (and perhaps treated) to examine the effect on target expression by IF-ICC, cells may be seeded ... tidewater timber homes
【流式学习】 Ki-67 检测细胞增殖protocol - 知乎 - 知乎专栏
WebRecipe. Dissolve 8g of NaCl, 0.2g of KCl, 1.44g of Na 2 HPO 4, and 0.24g of KH 2 PO 4 in 800ml distilled H 2 O. Add 20 ml of heat inactivated FBS. Add 0.9 grams of sodium … http://www.protocol-online.org/biology-forums/posts/34558.html WebMar 1, 2024 · 进行流式分析时经常使用的五种缓冲液的基本配方。. 但请注意:缓冲液可能需要根据细胞类型和应用进行优化。. 流式染色缓冲液(FACS缓冲液). 基本的FACS缓冲 … tidewater tides schedule