FIXATIONandDNAStainingforCellCycleAnalysis

BackgroundThis method of DNA staining utilizes ethanol to fix the cells and permeabilize the membrane, which allows the dye (Propidium Iodide) to enter the cells. Propidium Iodide (PI) is a DNA-binding fluorochrome that intercalates in the double-helix. Ribonuclease-A is used to eliminate the staining of double-stranded RNA.Generally, the method can be combined with the procedures for direct labeling or&nbs......阅读全文

FIXATION-and-DNA-Staining-for-Cell-Cycle-Analysis

BackgroundThis method of DNA staining utilizes ethanol to fix the cells and permeabilize the membrane, which allows the dye (Propidium Iodide) to ente

CELL-CYCLE-ANALYSIS

PROPIDIUM IODIDE: The most commonly used dye for DNA content/cell cycle analysis is PROPIDIUM IODIDE (PI). It can be used to stain whole cells or isol

Flow-Cytometric-Analysis-of-Cell-Cycle

Fixation1) Collect 2 X 106 cells.2) Pellet cells by spinning at 1,000 rpm, 4°C for 5 minutes.3) Resuspend cell pellet in 1 ml of cold PBS.4) Fix cells

Cell-Cycle-Staining-ProtocolDAPI

1. Harvest cells- wash 2X in PBS to get rid of serum proteins. 1200rpm, 5 min2. Resuspend pellet (up to 3x106 cells) in 1.2 ml PBS (Ca and Mg free).3.

Cell-cycle-analysis-of-Escherichia-coli-cells

Cell cycle analysis of Escherichia coli cellsC period = the time for a round of chromosome replicationD period = the time between the end of a round o

流式细胞仪技术专辑

Flow Cytometry Analysis (Springer Lab, Harvard University) Flow cytometry employs instrumentation that scans single cells flowing past excitation sour

DNA-Cell-Cycle

Solutions70% ethanolribonuclease (100 µg/ml DNase free, Sigma)propidium iodide ( 50 µg/ml in PBS)ProcedureHarvest cells. Spin at 1200 rpm for 5 minute

流式细胞仪技术专辑

 最方便的实验干货查询工具微信扫码进入「丁香实验」小程序编辑: 呜咽分享到:      Flow Cytometry Analysis (Springer Lab, Harvard University)Flow cytometry employs instrumentation that scan

Combined-Flow-Cytometric-Measurement-of-Two-CellSurface-Antigens2

DNA and RNA Staining6. Stain cells with 7-AAD: i. Resuspend the cells from Step 5 in 0.5 mL of NASS containing 10 µg/mL of 7-AAD. Incubatefor 20 min a

Vybrant®-DyeCycle™-Ruby-stain

实验概要Live cell studies  of cellular DNA content and cell cycle distribution are useful to detect  variations of growth patterns due to a variety of phy

细胞周期试剂盒Cell-cycle-staining-Kit中文操作步骤

试剂盒特点:1、独创的活细胞一步法检测,收集——洗涤——染色,简单快速   2、兼容固定细胞检测,改进的固定方法,更少细胞粘连,更小CV值   3、兼容流式和荧光显微镜分析,提供详细protocol固定细胞处理:1、收集细胞悬液,细胞数为2 × 10^5 ~ 1 × 10^6。离心沉淀细胞,去上清,

Protocol-for-intracytoplasmic-staining-of-cytokines-for-FACS-analysis

DescriptionProtocol for intracytoplasmic staining of cytokines for FACS analysis Procedure1) Prepare spleen, lymph node or T cell clone cells as singl

Staining-Procedure-for-Flow-Cytometric-Detection-of-Human-Cyclins

Staining Procedure for Flow Cytometric Detection of Human CyclinsThis is a standard protocol used at Pharmingen for Quality Control testing of the ant

细胞周期的流式细胞伩检测实验方法(PI,Brdu)2

B.3. COMMENTARY B.3.1 Background information The critical steps in the methodology are cell fixation, permeabilization and the concentrations of anti-

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement

IntroductionApoptosis is a normal physiological phenomenon put forward by Kerr [1]. It plays an important role in embryonic development, maintenance o

Vybrant®-DyeCycle™-Violet-Stain

实验概要Live cell studies  of cellular DNA content and cell cycle distribution are useful to detect  variations of growth patterns due to a variety of phy

Vybrant®-DyeCycle™-Green-and-Orange-Stains

实验概要Live  cell studies of cellular DNA content and cell cycle distribution are  useful to detect variations of growth patterns due to a variety of  ph

细胞周期的流式细胞伩检测实验方法(PI,Brdu)1

ANALYSIS OF CELL CYCLE Miriam Capri and Daniela Barbieri Dept. Biomedical Sciences, Sect. General Pathology,Via Campi, 287, University of Modena, 4110

Detection-of-Intracellular-Antigens-by-Flow-Cytometry

实验概要Fix and Perm  reagents are designed for use with all commercially available flow  cytometers. Alignment and compensation should be performed accor

Staining-Methods-for-cell

death Z. Xia 10/2/95The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidiu

Intracellular-Cytokine-Staining-Protocol

实验概要A  modification of the basic immunofluorescence staining and flow  cytometric analysis protocol can be used for the simultaneous analysis  of surf

Cyclins-and-Cell-Cycle-Regulation

The cell cycle is regulated by the interplay of many molecules. Key among these are the cyclins which are expressed and then degraded in a concerted f

Staining-Methods-for-cell-death

The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidium iodide)-red, dead

Immunofluorescent-Staining-of-Mouse-and-Rat-Leukocytes

I. ProcedureHarvest cells from tissue, preparing a single cell suspension. Red blood cells may be removed by lysis or density gradient: Red blood cell

Peripheral-blood-“endothelial-progenitor-cells”

EPC Isolation and Characterization1. EPCs were obtained by isolating mononuclear cells using Ficoll density-gradient centrifugation of human blood buf

Immunofluorescence-Labeling-of-Cells

实验概要Antibodies are an  important tool for demonstrating both the presence and the subcellular  localization of an antigen. Cell staining is a very ver

Yeast-Cell-Cycle-by-Flow-Cytometry

ReagentsCold absolute ethanol.0.5 M Na citrate stock (filtered), 50mM diluted stock.10 mg/ml RNase A (Boil 10 mins, cool, filter and store at -20°C).4

Simultaneous-analysis-of-DNA-content

Simultaneous analysis of DNA content and surface immunophenotype using gentle ethanol fixation techniques.  William Telford. Louis E. King and Pamela

Cell-Surface-Immunofluorescence-Staining-Protocol

实验概要A method of identifying  and enumerating specific cell types in a heterogeneous population of  cells by enhancing the specific staining of desired

Application-Note:-Qdot®-Nanocrystal-Conjugates-in-Flow-Cytometry

实验概要Researchers today  are trying to maximize the information that they get out of flow  cytometry experiments by looking at more parameters in a sing