CMFDALabelingofPlatelet

OUTLINECMFDA (5-chloromethylfluorescein diacetate) is a lipophilic tracer that has an enormous advantage over ordinary tracers (e.g. FITC) because it can be introduced into live (!) cells. Once inside the cell this dye undergo some covalent changes restricting from its passgae to extracellular milieu. PROTOCOLCollect blood and purify platelets.Resuspend in the certain known volume of BSGC and count platelets. Se......阅读全文

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

Platelet-Preparation

OUTLINEIn order to avoid platelet activation all manipulations must be performed as quickly and as acurate as possible.Work on ice if possible! This p

ELISA-with-Platelet

OUTLINEThis modification of qualitative ELISA (Enzyme-Linked Immunosorbent Assay) is used for either screening detection of anti-platelet antibodies o

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.

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

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

TUNEL-labeling

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

Western-Blot-with-Platelet-Protein

OUTLINEWestern blot is a wide used technique to identify a target protein/s for the certain antibody.PROTOCOLPrepare platelets.Lyse washed platelets (

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

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

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

Coating-of-Platelets-with-Antibody-in-vitro

OUTLINEAntibody-coated platelets (opsnized) may be used in the subsequent thrombophagocytosis assay. PROTOCOLResuspend 1.6x10^8 of CMFDA-labeled plate

Platelet-Amyloid-Precursor-Protein-Pathway

The amyloid -beta peptide (Ab), a proteolytic fragment of amyloid precursor protein (APP), is the major componenet of senile plaques, the hallmark of

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

Plateletassociated-Ig-(PAIg)-Elution

OUTLINEPlatelet-associated Ig (PAIg) could be eluted from the platelets. As a result of this procedure platelets get destroyed and the eluted Ig is fo

Eph-Kinases-and-ephrins-support-platelet-aggregation

Eph kinases are a family of receptor tyrosine kinases with an extracellular domain that binds their ligand, the ephrins, and an intracellular kinase d

Basic-Method-for-Indirect-Immunofluorescence-Labeling

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

Aspirin-Blocks-Signaling-Pathway-Involved-in-Platelet-Activation

Activation of the protease-activated GPCRs in platelets contributes to platelet activation in clotting. The protease-activated receptors PAR1 and PAR4

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-,

ThiolReactive-Probe-Labeling-Protocol

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

In-Situ-Cell-Death-(Apoptosis)-Detection-by-TUNEL-labeling

Protocol for Frozen Sections:Warm 150ml 4% Paraformaldehyde/1x PBS to RT. Fix slides in it, 20 min., RT.1x PBS rinse, 2 times.1x PBS, 30 min., RT. Beg

Protocol-for-Dual-Pulse-Labeling-Using-EdU-and-BrdU-Incorporation

实验概要The measurement of  cell proliferation is fundamental to the assessment of cell health,  genotoxicity, and drug efficacy. Proliferation is traditi

AA--Metabolite-Quantitation-of-Media-PostAA-Labeling

1) Remove 2 500 µl aliquots of supernatant into scintillation vials, add scintillation fluid and count.2) Aliquot 1.6 mls of the remaining supernatant

AA--Metabolite-Quantitation-of-Cell-Pellets-PostAA-Labeling

Extraction:1) Following spin, save supernatant for analysis. Be extremely careful not to disturb the pellet since it is somewhat dispersed.2) Immediat

E.coli-Total-RNA-Labeling-Protocol-for-Spotted-Microarray

Note:Start with 20 ug of total RNA for each labeling reaction.All solutions that can be filtered should be filtered.Cy dyes are light sensitive and sh

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

[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

DNA标记

DNA标记(主要内容如下)  DNA Labeling by Nick Translation  Random Primed Labeling  End-Labeling  Purification of Labeled DNA  Non-isotopic Labeling  OthersDNA L

机采冰冻血小板的临床应用及分析

[摘要] 目的:探讨冰冻血小板在血小板减少性疾病中应用的有效性与安全性。方法:随机选择318例血小板减少症患者,204例患者给予冰冻血小板输注,114例患者给予新鲜血小板输注,输注前及输注后18 h~24 h分别测定血小板计数,比较血小板回收率及临床出血症状改善情况。结果:冰冻血小板止血有效