IntracellularCytokineStainingProtocol

实验概要A modification of the basic immunofluorescence staining and flow cytometric analysis protocol can be used for the simultaneous analysis of surface molecules and intracellular cytokines at single-cell level. In this protocol, cells are first activated in vitro, stained for surface antigens, as in the regular staining protocol, then fixed and permeabilized to allow for anti-cytok......阅读全文

Wholemount-staining-of-embryos

Fix embryos in formalin or MEMFA for one hour at room temperature with mixing. Rinse with TBS, replace with methanol, store at -20oC.Rehydrate by slow

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

Protein-Staining-Procedures

This method was successful in our lab using prostate tissue and for our specific objectives. Investigators must be aware that they will need to tailor

Alkaline-phosphatase-staining

4.5.1.1 General informationEndothelial cells possess an endogenous alkaline phosphatase (AP) activity. The enzymatic activity of AP is not restricted

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

Silver-Staining-Protocol

1x 40min - overnight     50% MeOH, 12% Acetic Acid1x 30min                                  50% MeOH, 12% Acetic Acid, 0.05% 37% Formaldehyde3x 20min 

Intracellular-Staining-Protocol

1. Fix cells- Add16% formaldehyde directly into culture medium to obtain a final concentration of 1.5% formaldehyde.2. Incubate in fixative for 10 min

Actin-StainingActin-Staining-Protocol

实验概要Invitrogen  offers several fluorescent and biotinylated phalloidin and phallacidin  derivatives for labeling F-actin. These phallotoxins, isolated

Direct/Indirect-Staining-Protocol

Use this Protocol for Directly or Indirectly staining cells for Flow Cytometric Analysis1) Dilute cells to 5x10^6 cells/mL2) Aliquot 100uL of cells pe

Preparation-and-Staining-of-Paraffin-Sections

I. Fixation and Processing of Tissue for Paraffin SectionsA. Fixation of Tissues in 10% Neutral Buffered FormalinSacrifice animal by prescribed and ap

Blood-Smear:-Preparation-and-Staining

Blood Smear: Preparation and StainingReference:Davidson, I. and Henry J., Clinical Diagnosis by Laboratory Methods, I. Davidsohn and J. Henry, eds., W

High-resolution-negative-staining

High resolution negative staining(From Valentine et al, 1968. Biochemistry 7:2143-52)Rationale: For the highest resolution with negative staining, the

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

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

Gramstaining-Procedure

Gram-staining is a four part procedure which uses certain dyes to make a bacterial cell stand out against against its background. The specimen should

Intracellular-Immunofluorescent-Staining-for-Flow-Cytometry

IntroductionA modification of the basic immunofluorescent staining and flow cytometric analysis protocol can be used for the simultaneous analysis of

Preparation-and-Staining-of-Frozen-Tissue-Sections

I. Preparation of Frozen Sections for SectioningMaterials neeed:2-methylbutane (isopentane)Liquid NitrogenDry icePeel-Away?/sup> base moldsFrozen tiss

SSR-GEL-and-Silver-Staining-Protocol

I. EQUIPMENT:DNA sequencing unit (35 x 45 cm) & 2000V power supplyClampsLg. plastic trays (4), about 43 x 50 x 8 cm, and one lidTwo rocking platformsH

Methylene-Blue-DNA-staining-protocol

Methylene Blue DNA staining protocolProtocol:Load 2-5X the amount of DNA that would give bands of moderate intensity on an ethidium bromide stained ge

Immunofluorescent-staining-of-Sea-Urchin-embryos

1. Transfer fixed embryos to microfuge tubes. Allow to settle for 10 minutes.Gently remove most of the liquid.2. Add 100 ul antibody to one tube and 1

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

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

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

Immunofluorescent-Staining-of-Drosophila-Larval-Brain-Tissue

实验概要The Drosophila larval brain is a well-established model for investigating the role of stem cells in development. Neuroblasts (neural stem cells)

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

Immunofluorescent-Staining-of-Drosophila-Larval-Brain-Tissue

INTRODUCTIONThe Drosophila larval brain is a well-established model for investigating the role of stem cells in development. Neuroblasts (neural stem

Preparation-of-fixed-embryos-for-immunocytochemistry-and-AP-staining

1. Transfer 50 ml of embryo cultures to centrifuge tubes. Spin at 1500 rpm for 5 minutes. Check that you can see a pellet of embryos at the bottom.Qui

细菌的芽孢染色(spore-staining)

实验原理细菌的芽胞具有厚而致密的壁,透性低,不易着色,若用一般染色法只能使菌体着色而芽胞不着色(芽孢呈无色透明状)。芽孢染色法就是根据芽孢既难以染色而一旦染上色后又难以脱色这一特点而设计的。所有的芽孢染色法都基于同一个原则:除了用着色力强的染料外,还需要加热,以促进芽孢着色。当染芽孢时,菌体也会着色

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.

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