SimultaneousanalysisofDNAcontent

Simultaneous analysis of DNA content and surface immunophenotype using gentle ethanol fixation techniques. William Telford. Louis E. King and Pamela J. Fraker Michian State University, East Lansing, MI Hospital for Special Surgery, New York, NYA major issue in the simultaneous analysis of DNA content using DNA binding dyes and cell surface immunophenotyping using fluorochrome-conjugated antibodie......阅读全文

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

Flow-Cytometry-of-Fibroblast-Nuclei-for-DNA-content

MaterialsP.I. Solution: 4 mM Na3Citrate (0.118 g/100 mL)30 U/mL RNAseI (43 mg/100 mL)0.1% Triton-X100 (0.1mL/100 mL)50 µg/mL propidium iodide (5 mg/10

Measurement-of-GFP-Expression-and-DNA-Content-in-Permeabilized-Cells

ReagentsCells to be studied expressing green fluorescent protein (GFP). Note that the same cell type without GFP is needed as a control.1 X PBS2% Buff

Molecular-Analysis-and-Results--DNA

Theory of CGHComparative genomic hybridization (CGH) is a fairly new molecular cytogenetic technique that allows detection of DNA sequence copy number

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

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

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

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

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement2

TroubleshootingCritical Steps(1) Don’t trypsinize cells for too long when collecting them.(2) Rotation speed should be no more than 1500 rpm during ce

QUALITATIVE-ANALYSIS-OF-DNA-FRAGMENTATION-BY-AGAROSE-GEL-ELECTROPHORESIS

1. IntroductionNuclear morphology changes characteristic of apoptosis appear within the cell together with a distinctive biochemical event: the endonu

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™-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

QUALITATIVE-ANALYSIS-OF-DNA-FRAGMENTATION-BY-AGAROSE-GEL-ELECTROPHORESIS2

3. Commentary    3.1. Background informationApoptosis is an innate mechanism of eukariotic cell suicide which plays a major role in many physiological

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

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

Glycosphingolipid-analysis

1) Incubate cells with 1 µCi/ml of 3H-galactose for 72 hours.---> If treatment is for an extended period of time: treat in serum free media containing

Lipid-analysis

Thin layer chromatography is based on the separation of a mixture of compounds as it migrates with the help of a suitable solvent through a thin layer

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

PEGMediated-Protoplast-Transformation-with-Naked-DNA

Direct introduction of DNA into plant protoplasts facilitates a rapid analysis of transient gene expression, as well as the generation of stably t

Flow-Cytometry-Analysis

PurposeFlow cytometry employs instrumentation that scans single cells flowing past excitation sources in a liquid medium. The technology can provide r

Analysis-of-Heme-and-Hemoproteins

Heme is perhaps the most ubiquitous cofactor found in nature and the most functionally diverse. Hemoproteins are involved in cell respiration (cyt

Biosynthesis-and-Analysis-of-Bilins

The term bilin is a collective one to describe a broad group of open chain tetrapyrroles and derives from the name “bile pigments” as the first of

Lineage-Analysis-of-Blood

Materials:Capillary tubes1.5 mL Eppendorf microfuge tubes15 mL conical centrifuge tubes96-well V-bottom plates (Corning Costar 3894, from Fisher)Flow

Analysis-of-murine-BM

Histologic analysis of murine BM is a necessary complement to flow cytometric or in vitro analysis. Techniques to do this are well established in huma

Analysis-of-Oligosaccharide-Ligands

Analysis of Oligosaccharide Ligands by High Performance Liquid Affinity ChromatographyAnalysis of Oligosaccharide Ligands by High Performance Liquid A

流式应用精选——微核检测(体内体外)

 注:点击文章名称查看详情。文章名称样本仪器型号备注Assessment of the Genotoxic Potential of Azidothymidine in the Comet,Micronucleus, and Pig-a AssayBone Marrow and Peripheral

DualColor-ELISPOT-Assay-for-the-Simultaneous-Detection2

21. Add 100 µL of developing buffer to all wells using a multichannel pipette and incubate at room temperature for at least 2 h. 22. Wash the ELISPOT

DualColor-ELISPOT-Assay-for-the-Simultaneous-Detection1

Dual-Color ELISPOT Assay for the Simultaneous Detection of IL-2 and/or IFN- Secreting T CellsINTRODUCTIONThe enzyme-linked immunospot (ELISPOT) assay

Analysis-and-Reconstitution-of-Phycobiliproteins:-Methods-for-the-...

Analysis and Reconstitution of Phycobiliproteins: Methods for the Characterization of Bilin Attachment ReactionsPhycobiliproteins are a homologous fam

Genomic-Southern-Blot-Analysis

This chapter describes a detailed protocol for genomic Southern blot analysis which can be used to detect transgene or endogenous gene sequences i