ImmunofluorescenceLabelingofCells

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 versatile technique and, if the antigen is highly localized, can detect as few as a thousand antigen molecules in a cell. In some circumstances, cell staining may also be used to determine the approximate concentration of an antigen, espec......阅读全文

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

Basic-Method-for-Indirect-Immunofluorescence-Labeling

Basic Method for Indirect Immunofluorescence LabelingBackgroundThis is the method for indirect immunofluorescence labeling; that is, the antibodies do

Immunofluorescence-Microscopy-of-tissue-culture-cells

Immunofluorescence Microscopy of tissue culture cellsThese methods are written for direct staining of filamentous actin with bodipy FL-phallicidin and

Metabolic-Labeling-of-Cells-with-35S

1) Transfer to a 24 wells plate the desired colonies.2) Once the cells are attached (at least 8 hours after tripsinizing them) add ~1 ml ofDME (met-,

Sphingomyelin-Quantitation-Postcholine-Labeling-of-HL60-Cells

Lipid Extraction1) Following the appropriate time of treatment, transfer 4.5 ml into each of two duplicate glass pyrex tubes and maintain on ice.2) Sp

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

[3H]-Choline-Labeling-and-TNF-Treatment-of-HL60-Cells

1) Grow cells to a density of 5-8 X 105 cells/ml in RPMI 1640 containing serum.2) Pellet cells and wash 1 time with room temperature PBS.3) Resuspend

Labeling-Tubulin-and-Quantifying-Labeling-Stoichiometry

Labeling Tubulin and Quantifying Labeling StoichiometryThis is a general procedure for coupling moieties with reactive succinimidyl esters to tubulin.

细胞组分和细胞器——细胞骨架

Fixation and Immunofluorescence of the Cytoskeleton (Mitchison Lab)  Recycling Tubulin (Mitchison Lab)  Labeling Tubulin and Quantifying Labeling Stoi

Immunofluorescence-...

实验概要Immunofluorescence  is a technique used for light microscopy with a fluorescence microscope  and is used primarily on biological samples. This tec

Labeling-Tubulin-and-Quantifying-Labeling-Stoichiometry2

II. Labeling ProtocolThe procedure described below can be scaled down if desired. It is essential to perform all steps involving caged dyes under a sa

TUNEL-labeling

In Situ Cell Death (Apoptosis) Detection by TUNEL labelingby Boehringer Mannheim (Catalog No. 1684809), modified by Josiah N. Wilcox andJosé C. Rodrig

Biosynthetic-labeling

How long should cells be labeled? The ideal length of time to label cells depends on the protein of interest and the label that you are using. If you

免疫组织化学

·         Double Peroxidase (HRP) Immunohistochemical Labeling of Trypsin-Sensitive Antigens (KPL)·         Immunohistochemistry (Tyner lab)This is a

Arachidonic-Acid-Labeling

1) Grow cells to a density of 5-8 X 105 cells/ml in RPMI 1640 containing serum.2) Pellet cells and wash 1 time with room temperature PBS.3) Resuspend

BrdU-Labeling-Protocol

实验概要The thymidine analog, 5-bromo-2-deoxyuridine (BrdU),is a common reagent used for cell proliferation assays and for the detection of apoptotic

Detection-by-TUNEL-labeling

In Situ Cell Death (Apoptosis) Detection by TUNEL labelingby Boehringer Mannheim (Catalog No. 1684809), modified by Josiah N. Wilcox,José C. Rodriguez

CMFDA-Labeling-of-Platelet

OUTLINECMFDA (5-chloromethylfluorescein diacetate) is a lipophilic tracer that has an enormous advantage over ordinary tracers (e.g. FITC) because it

Yale-Immunofluorescence-Protocol

实验概要We provide a protocol for fixation, immunostaining, and imaging in 384-well Plates.主要试剂Reagents1. 384-well view plates (Aurora)2. HUVEC (pooled, L

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

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

Methanol-Fixation-for-Immunofluorescence

Methanol fixation works by precipitating proteins, and as such it is a quick method (2-5)minutes is enough time for most antibodies/proteins). Diffuse

免疫细胞化学

Introduction to Immunocytochemistry (House Ear Institute)A brief overview of common available methods.  BrDU Immunocytochemistry using peroxidase and

DNA-labeling-by-nick-translation

DNA labeling by nick translationreagents: DNA for labeling (concentration c > 150 ng/µl) modified nucleotides: Biotin-16-dUTP, Digoxigenin-11-dUTP, co

Immunofluorescence-/-Confocal-Microscopy-Protocol

实验概要Immunofluorescence  is a technique used for light microscopy with a fluorescence microscope  and is used primarily on biological samples. This tec

Immunofluorescence-/-Confocal-Microscopy-Protocol

实验概要Immunofluorescence  is a technique used for light microscopy with a fluorescence microscope  and is used primarily on biological samples. This tec

Double-immunofluorescence:-sequential-protocol

实验概要We provide a protocol for immunofluoresent double staining incubating the antibodies separately.实验步骤1. Blocking and sequential incubation    1) Fi

immunofluorescence-of-general-cell-by-Peprotech

实验概要The following protocol provides a method of immunofluorescence of general cell by Peprotech.实验步骤Please refer to the antibody Product Information S

immunofluorescence-of-general-PBMC-by-Peprotech

实验概要The following protocol provides a method of immunofluorescence of general PBMC by Peprotech.实验步骤The following protocol used human PBMC that were