FluorescentStainingofCells

1. Fluorescent phalloidin in methanol. Phallacidin does not work as well. Dilute 10 ul 330 nM stock into 500 ul PBS for each large coverslip.2. PBS, solution A.Procedure:1. Fix and permeabilize cells (see other protocols). Mount coverslip onto a plastic frame reserved for fixed samples. Apply some vacuum grease to the frame before use, if necessary.2. Turn off light. Dilute fluorescent phalloidin 50x into PBS......阅读全文

Fluorescent-Staining-of-Cells

1. Fluorescent phalloidin in methanol. Phallacidin does not work as well. Dilute 10 ul 330 nM stock into 500 ul PBS for each large coverslip.2. PB

Betagal-staining-of-eukaryotic-cells-in-vitro

(Modification of methods of Dr. Seong-Seng Tan and Promega's "Protocols and Applications Guide")Cells previously transfected with a lac Z construc

LIVE/DEAD®-Violet-Viability/Vitality-Kit

实验概要The  LIVE/DEAD® Violet Viability/Vitality Kit provides a two-color  fluorescence cell viability and vitality assay that is based on the  simultane

LIVE/DEAD®-Violet-Viability/Vitality-Kit

实验概要The LIVE/DEAD®  Violet Viability/Vitality Kit provides a two-color fluorescence cell  viability and vitality assay that is based on the simultaneo

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

LIVE/DEAD®-Fixable-Dead-Cell-Stain-Kits

实验概要The  LIVE/DEAD® Fixable Dead Cell Stain Kits use a novel method to evaluate  the viability of mammalian cells by flow cytometry. These assays are

LIVE/DEAD®-Fixable-Dead-Cell-Stain-Kits

实验概要The LIVE/DEAD®  Fixable Dead Cell Stain Kits use a novel method to evaluate the  viability of mammalian cells by flow cytometry. These assays are

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

3-Color-Staining:-AlphaCatenin-in-HeLa-Human-Cervical-Cancer-Cells

实验概要Alpha-catenin  in HeLa human cervical cancer cells was labeled using mouse  anti-α-catenin and visualized with Alexa Fluor® 488 goat anti-mouse Ig

Early-development-of-primary-motor-neurons-and-somites-in-Zebrafish-Embryos

Background:Zebrafish,or the teleost fish Danio rerio,is a rapidly developing organism that is apopular species for studying vertebrate development. Cl

DAPI-Counterstaining-Protocols

实验概要The  blue-fluorescent DAPI nucleic acid stain preferentially stains dsDNA;  it appears to associate with AT clusters in the minor groove. Binding

Flow-Cytometry-Analysis

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

DAPI-Nucleic-Acid-Stain

实验概要The  blue-fluorescent DAPI nucleic acid stain preferentially stains dsDNA; it  appears to associate with AT clusters in the minor groove. Binding

Fluorescence-Procedures-fortheActin-andTubulin-Cytoskeleton-in-Fixed-Cells2

Formaldehyde FixationFix in 4% formaldehyde (16% stock EM grade) in CBS for 20 minutesRinse in TBSPermeabilize as for methanol fixationProcede as for

ex-vivo-expanded-endothelial-progenitor-cells

Cell Culture. 1. Total hPBMCs were isolated from blood of human volunteers by density gradient centrifugation. 2. Cells were plated on culture dishes

Fluorescence-Procedures-forthe-ActinandTubulin-Cytoskeleton-inFixed-Cells2

Actin CytoskeletonMethanol fixationFix in -20oC methanol for 1-2.5 minutesRinse in TBSPermeabilize in TBS-0.5% TX for 10 minutesRinse in TBS-0.1% TX (

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

线粒体荧光探针大全:TMRM,Mitotracker,JC1(1)

线粒体荧光探针信息大全 (Probes for Mitochondria)包括各种常用探针,如JC-1,JC-9,TMRM,TMRE等Mitochondria are found in eukaryotic cells, where they make up as much as 10% of th

The-Effects-of-Ultraviolet-Light-on-the-Fertilization

Jill K. Flemming, Franklin & Marshall College, Class of 2001IntroductionThe objective of this project is to observe the effects of UV radiation on bot

线粒体肿胀检测方法

Estimating Mitochondrial Mass,可以用于线粒体肿胀的检测Accurate measurements of mitochondrial mass require a probe that will accumulate in mitochondria regardless

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

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

Dual-and-TripleCo...-(二)

主要试剂1. Blocking reagent after coating: 10% fetal calf serum (FCS) in phosphate-buffered saline (PBS), pH 7.4.2. Cells suspended in complete culture me

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

线粒体荧光探针大全:TMRM,Mitotracker,JC1(2)

MitoTracker Green FM ProbeMitochondria in cells stained with nanomolar concentrations of our patented MitoTracker Green FM dye (M7514) exhibit bright

Measurement-of-Green-Fluorescent-Protein-Expression

 ReagentsCells to be studied expressing green fluorescent protein (GFP). Note that the same cell type without GFP is needed as control.Hoechst 33342 s

线粒体荧光探针大全:TMRM,Mitotracker,JC1(4)

Nonyl Acridine OrangeNonyl acridine orange (A1372) is well retained in the mitochondria of live HeLa cells for up to 10 days, making it a useful probe

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

Immunofluorescence-Microscopy-Protocol

实验概要Immunofluorescence  allows the imaging of a specific factor in cells or tissue sections  through the use of a specific antibody chemically which i