FACSAnalysisUsingPeripheralBloodCells

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 immediately to prevent clotting. Keep tubes on ice.Remove RBCs from samples. This can be accomplished by several means. At The Jackson Laboratory, RBCs are lysed using either Gey's solution or a buffered ammonium chloride (ACK) solution. (Alternatively, Becton-Dick......阅读全文

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

Preparation-Of-Peripheral-Blood-Cells-For-Chromosome-Analysis

实验概要Lymphocytes  are differentiated cells which normally do not undergo subsequent cell  divisions. By culturing lymphocytes in the presence of a mito

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

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

Culture-of-Peripheral-Blood-Lymphocytes-for-Chromosome-Analysis

实验概要Provide information about chromosomal abnormalities.实验原理The  blood cell karyotyping method was developed to provide information  about chromosomal

Isolation-of-peripheral-blood-mononuclear-cells-(PBMC)

1. Acid-citrate dextrose-treated blood (450 ml) was obtained from donors. 2. PBMC were isolated by centrifugation over lymphocyte separation medium. 3

流式应用精选——微核检测(体内体外)

 注:点击文章名称查看详情。文章名称样本仪器型号备注Assessment of the Genotoxic Potential of Azidothymidine in the Comet,Micronucleus, and Pig-a AssayBone Marrow and Peripheral

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

Harvesting-lymphocytes-from-Peripheral-Blood

Blood Harvest·        Anesthetize mice with 50ml of Xylene-Ketamine(2:1) coctail·        Pin animal to a board (use distal extremities) supine·       

Lineage-Analysis-of-Blood

Materials:Capillary tubes1.5 mL Eppendorf microfuge tubes15 mL conical centrifuge tubes96-well V-bottom plates (Corning Costar 3894, from Fisher)Flow

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

红细胞裂解的实验方法步骤

IntroductionPrior to using lymphoid tissue cell suspensions for flow cytometric analysis and/or for in vitro functional assays, it is recommended to r

Human-Peripheral-Blood-Mononuclear-Cell-Preparation

This protocol describes a procedure for isolating human peripheral blood mononuclear cells (lymphocytes and monocytes) from a Buffy Coat (obtained fro

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

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

Transfection-of-Mammalian-Cells-Using-Lipofectamine

Materials:       LipofectamineBasal Medium containing 10% fetal bovine serum, 1% glutamine, 1% aaBasal Medium containing 1% glutamineBasal Medium cont

细胞组分和细胞器——染色体

Chromosomal DNA Prep : cultured cells/tissue samples (Mike A Dyer)This protocol was developed for cultured cells but should be appropriate for dissoci

细胞遗传学——染色体

Chromosome Staining and Banding Technique (Primate Cytogenetics Network)Protocols for different staining method, each is in great detail.  Karyotype A

Protocol-for-Isolating-DNA-from-Blood-with-Nucleated-Red-blood-Cells

实验概要DNA  isolation from fish or avian blood sample can be difficult because it  contains nucleated red blood cells. E.Z.N.A. NRBC Blood DNA Kit is  de

Cell-cycle-analysis-of-Escherichia-coli-cells

Cell cycle analysis of Escherichia coli cellsC period = the time for a round of chromosome replicationD period = the time between the end of a round o

Transcriptome-Coexpression-Analysis-Using-ATTEDII-for-Integrated-...

Transcriptome coexpression analysis is an excellent tool for predicting the physiological functions of genes. It is based on the “guilt-by-associa

Detection-of-MicroRNA-Heterogeneity-in-Single-Cells-Using-an-Automated

Introduction  MicroRNA  (miRNAs) are short (18–24 nucleotides), non-coding RNAs that regulate  gene expression by both disrupting messenger RNA (mRNA

过敏性湿疹病人体内金黄色葡萄球菌内毒素对组...(一)

过敏性湿疹病人体内金黄色葡萄球菌内毒素对组胺和白三烯释放的研究过敏性湿疹病人体内金黄色葡萄球菌内毒素对组胺和白三烯释放的研究(国外学术刊物发表) Staphylococcus aureus Enterotoxins Induce Histamine and Leukotriene Release i

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

Heterogeneity-of-SingleCell-Gene-Expression-Across-Phenotypically(二)

 Figure 2: Verification of C1 Single-Cell mRNA-Seq data quality. a)ERCC  RNA Spike-In Control Mix 1 was applied to a C1 IFC at a total  transcript in

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

Analysis-of-Proteins-using-Small-Format-2D-Gel-Electrophoresis

Preparation of protein samplesIntracellular virus proteinsThe following method has been developed principally for the analysis of intracellular protei

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

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