ProtocolforintracytoplasmicstainingofcytokinesforFACSanalysis

DescriptionProtocol for intracytoplasmic staining of cytokines for FACS analysis Procedure1) Prepare spleen, lymph node or T cell clone cells as single cell suspension, using erythrocyte lysis (water) or Lymphopaque as appropriate. 2) Stimulate cells for 2 hours in vitro with 50 ng/ml PMA (Sigma, P8139) + 500 ng/ml ionomicin (Sigma I0634) in phenol red free RPMI 1640 medium + 10% fetal calf serum at 37 deg ......阅读全文

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

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

FACS-Analysis-of-ES-Cells

Isolate cells and dissociate to single cell suspension (can use Gibco Cell Dissociation Buffer, Accutase or Trypsin)Wash with 10% FBS/DMEM:F12For surf

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

Silver-Staining-Protocol

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

FACS-Analysis-Using-Peripheral-Blood-Cells

FACS Analysis Using Peripheral Blood CellsCollect blood (75 microliters) into 1ml PBS containing 5 microM EDTA (10 microliters of 0.5 M stock) and mix

免疫荧光

Immunofluorescence Technique (Spector Lab)protocol for immunofluorescence on cells  Immunofluorescence Protocol (Walter Steffen)Methanol fixationForma

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

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

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

信号传导

Cytokine Bioassays (eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c

信号传导

Cytokine Bioassays (eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c

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-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

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

流式细胞仪做血细胞

Collect blood (75 microliters) into 1ml PBS containing 5 microM EDTA (10 microliters of 0.5 M stock) and mix immediately to prevent clotting. Keep tub

流式细胞仪做血细胞

Collect blood (75 microliters) into 1ml PBS containing 5 microM EDTA (10 microliters of 0.5 M stock) and mix immediately to prevent clotting. Keep tub

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

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.

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

Dual-and-TripleCo...-(一)

实验概要Cytokine ELISPOT  has become a powerful routine tool for the analysis of disease- as well  as vaccine-induced T-cell responses. The method is limi

ImmunohistochemistyFluorescence-Protocol1

MaterialsCytokine-specific Primary Antibodiesunlabeled or biotinylated antigen-affinity purified polyclonal antibodies (R&D Systems ''AF'&

酵母遗传学技术

Genome-wide Gene Expression Analysis (Richard Young Research Group,Whitehead Institute for Biomedical Research)A genoe-wide gene expression analysis u

蛋白质电泳

蛋白质电泳(主要内容如下)One-Dimensional SDS-PAGETwo-Demensional SDS-PAGEProtein Electrophoresis in Agarose Gel Gel StainingRecipesOne-Dimensional SDS-PAGE·      

基因型分析

Randomly Amplified Polymorphic DNA (RAPD)Randomly Amplified Polymorphic DNA (RAPD) by  (DNA KAFFE)RAPD analysis has been successfully used in mapping

Cytokines-and-Inflammatory-Response

Inflammation is a protective response to infection by the immune system that requires communication between different classes of immune cells to coord

Regulation-of-hematopoiesis-by-cytokines

The process of hematopoesis is regulated by various cytokines. The combination of cytokines stimulates the proliferation and/or differentiation of the

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