IntracellularImmunofluorescentStainingforFlowCytometry
IntroductionA modification of the basic immunofluorescent staining and flow cytometric analysis protocol can be used for the simultaneous analysis of surface molecules and intracellular antigens at the single-cell level. In this protocol, cells are first activated in vitro, stained for surface antigens as in the surface antigen protocol, then fixed with paraformaldehyde to stabilize the cell membrane a......閱讀全文
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
Intracellular－Immunofluorescent－Staining－for－Flow－Cytometry2
Table 2: Human Cytokines: Intracellular Staining Quick GuideHuman Cytokines: Intracellular Staining Quick GuideHuman CytokineCell SourceActivationIncu
Detection－of－Intracellular－Antigens－by－Flow－Cytometry
實驗概要Fix and Perm ?reagents are designed for use with all commercially available flow ?cytometers. Alignment and compensation should be performed accor
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
Flow－Cytometry－Analysis
PurposeFlow cytometry employs instrumentation that scans single cells flowing past excitation sources in a liquid medium. The technology can provide r
Intracellular－Cytokine－Staining－Protocol
實驗概要A ?modification of the basic immunofluorescence staining and flow ?cytometric analysis protocol can be used for the simultaneous analysis ?of surf
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
流式細胞儀技術專輯
Flow Cytometry Analysis?(Springer Lab, Harvard University)?Flow cytometry employs instrumentation that scans single cells flowing past excitation sour
流式細胞儀技術專輯
?最方便的實驗干貨查詢工具微信掃碼進入「丁香實驗」小程序編輯：?嗚咽分享到：??????Flow Cytometry Analysis?(Springer Lab, Harvard University)Flow cytometry employs instrumentation that scan
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
Detection－Of－Cell－Viability－And/Or－Apoptosis－By－Flow－Cytometry－(FACS)
Viable?cells are cells that when allowed to continue beyond the timepoint of examination will stay alive. Besides live and healthy cells, cells in ear
流式細胞術（Flow－Cytometry,－FCM）
流式細胞術（Flow Cytometry, FCM）是一種在功能水平上對單細胞或其他生物粒子進行定量分析和分選的檢測手段，它可以高速分析上萬個細胞，并能同時從一個細胞中測得多個參數，與傳統的熒光鏡檢查相比，具有速度快、精度高、準確性好等優點，成為當代最先進的細胞定量分析技術。流式細胞儀（Flow C
流式細胞儀（Flow－Cytometry）
1 流式細胞儀的概念及其發展歷史1．1 流式細胞儀的基本概念 流式細胞儀（flow cytonletry，FCM）是對高速直線流動的細胞或生物微粒進行快速定量測定和分析的儀器，主要包括樣品的液流技術、細胞的計數和分選技術，計算機對數據的采集和分析技術等。流式細胞儀以流式細胞術為理論基礎，是流體力學、
流式細胞儀（Flow－Cytometry）
1?流式細胞儀的概念及其發展歷史1．1 流式細胞儀的基本概念 流式細胞儀（flow cytonletry，FCM）是對高速直線流動的細胞或生物微粒進行快速定量測定和分析的儀器，主要包括樣品的液流技術、細胞的計數和分選技術，計算機對數據的采集和分析技術等。流式細胞儀以流式細胞術為理論基礎，是流體力學、
Application－Note:－Qdot?－Nanocrystal－Conjugates－in－Flow－Cytometry
實驗概要Researchers today ?are trying to maximize the information that they get out of flow ?cytometry experiments by looking at more parameters in a sing
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
ICBR－Flow－Cytometry－Core－Laboratory－Paraformaldehyde－Fixation－of－Cells
BackgroundThis fixation method is good for cells labelled by fluorochrome-conjugated antibodies to membrane antigens. It will stabilize the light scat
ASENSITIVE－METHOD－FOR－DETECTION－OF－APOPTOSIS－BY－SINGLE－LASER－FLOW－CYTOMETRY
MATERIALS:1. 1 X PBS (PBSAz, 1 X PBS, e.g., Irvine Scientific, CA, containing 2% newborn calf serum and 0.1% sodium azide)2. 7-Amino-actinomycin D (7-
免疫熒光
Immunofluorescence Technique?(Spector Lab)protocol for immunofluorescence on cells??Immunofluorescence Protocol?(Walter Steffen)Methanol fixationForma
信號傳導
Cytokine Bioassays?(eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c
信號傳導
Cytokine Bioassays?(eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c
細胞組分和細胞器——細胞器分離
Labeling Microtubules?(Molecular Dynamics Inc.??)Microtubules are involved in many aspects of cell motion including propulsion, mitosis, growth, and o
LIVE/DEAD?－Fixable－Dead－Cell－Stain－Kits
實驗概要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
specific－immunodetection－of－cyclins－using－488/630－dual－laser－flow－cytometry
Phenotype-specific immunodetection of cyclins using?488/630 nm dual laser flow cytometryWilliam Telford?Hospital for Special SurgeryThis protocol is f
LIVE/DEAD?－Violet－Viability/Vitality－Kit
實驗概要The LIVE/DEAD? ?Violet Viability/Vitality Kit provides a two-color fluorescence cell ?viability and vitality assay that is based on the simultaneo
LIVE/DEAD?－Violet－Viability/Vitality－Kit
實驗概要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?－Fixable－Dead－Cell－Stain－Kits
實驗概要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
流式細胞儀(Flow－Cytometry):鎦金歲月50年
自從50年前誕生至今，流式細胞儀（Flow cytometry）一直并仍然是無以倫比的高通量、高內涵的單細胞分析技術。 2015年11月，是流式細胞儀誕生50周年之時。人們可能會想象，一種如此長時間以前發明的技術應該到今天會是徹底地不同于當年，但是事實不然，它的基礎原理與結構幾乎沒有什么改變，
ImmunohistochemistyFluorescence－Protocol1
MaterialsCytokine-specific Primary Antibodiesunlabeled or biotinylated antigen-affinity purified polyclonal antibodies (R&D Systems ''AF'&
Combined－Flow－Cytometric－Measurement－of－Two－CellSurface－Antigens
INTRODUCTIONFlow cytometry is frequently used to assess nucleic acid content?in individual cells. Based on DNA content alone, however, cells?in the qu