FluorescenceMountingMedium(Antifade)
Materials Needed20ml glass scintillation vialSmall stir barFoilGlycerol1X PBSPipets* P-phenylenediamine ( EMD Chemicals Inc. Cat# PX0730)Carbonate-Bicarbonate Buffer (see below)Wrap a glass scintillation vial with foil and drop in a small stir bar. (PPD is light-sensitive.)With a 10 ml pipet add 9 mls of glycerol to the vial.With the 1000 µl Pipetman add 1ml of 1X PBS.Place on stirrer and begin mixing.Weigh out 10 mg......阅读全文
Fluorescence-Mounting-Medium-(Antifade)
Materials Needed20ml glass scintillation vialSmall stir barFoilGlycerol1X PBSPipets* P-phenylenediamine ( EMD Chemicals Inc. Cat# PX0730)Carbonate-Bic
A-semipermanent-mounting-medium-for-immunofluorescence-microscopy
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免疫荧光
Immunofluorescence Technique (Spector Lab)protocol for immunofluorescence on cells Immunofluorescence Protocol (Walter Steffen)Methanol fixationForma
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· Double Peroxidase (HRP) Immunohistochemical Labeling of Trypsin-Sensitive Antigens (KPL)· Immunohistochemistry (Tyner lab)This is a
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Materials8% (w/v) paraformaldehyde stock solution: Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go highe
TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS
Materials8% (w/v) paraformaldehyde stock solution: Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high
TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS
Materials8% (w/v) paraformaldehyde stock solution: Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high
Basic-Fluorescent-in-situ-Hybridization-(FISH)
实验概要Fluorescence in situ hybridization method is a kind of physical map drawing method, use fluorescent element mark probe, to detect probe and spli
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
Immunohistochemistry-using-AntiGanglioside-Antibodies
Immunohistochemistry using Anti-Ganglioside AntibodiesTadashi Tai~Head, Department of Tumor Immunology, The Tokyo Metropolitan Institute of Medical Sc
ImmunohistochemistyFluorescence-Protocol2
Suitable for use on single-cell suspensions from peripheral blood, lymphoid tissue or cultured cell-lines.Sample Preparation and FixationHarvest cells
显微镜技术——光学显微技术
The Light Microscope (House Ear Institute)An explanation of how the light microscope works, how to use it, and how to get optimal results when using i
MS-Plant-Tissue-Culture-Medium
Component mg/l in MS mg/l in stock Amount for
MEDIUM-FOR-EMBRYO-RESCUE-(FOR-1-L)
Put 500 mL of distilled water in a 1-L beaker.Add the following:ucrose (6 % final concentration) – 30 gi-inositol (100 mg/L stock is 0.5 g/50 mL) – 10
显微镜技术——荧光显微技术
Immunofluorescencc Microscopy of tissue culture cells (Microscopy and Electronic Imaging Lab)These methods are written for direct staining of filament
Fluorescence-In-Situ-Hybridization-using-TSA™
实验概要This protocol describes steps for fluorescent in situ hybridization (FISH) to Drosophila embryos using Tyramide Signal Amplification (TSA™), and
mccoys-5A-medium是什么
McCoys 5A 培养基适合于多种类型的原代细胞、确立的细胞系以及移植的活检组织的增殖。该培养基适用于多种来源于正常骨髓、皮肤、脾脏、肾、肺、大鼠胚胎以及其他组织的哺乳动物细胞的原代培养。
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
Immunofluorescent-Staining-of-Drosophila-Larval-Brain-Tissue
INTRODUCTIONThe Drosophila larval brain is a well-established model for investigating the role of stem cells in development. Neuroblasts (neural stem
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Microscopes in Cell BiologyIntroductionMicroscopy has a major role in the study of cells. From the very beginning, researchers have tried to develop w
ImmunohistochemistyFluorescence-Protocol1
MaterialsCytokine-specific Primary Antibodiesunlabeled or biotinylated antigen-affinity purified polyclonal antibodies (R&D Systems ''AF'&
荧光分析法(fluorescence-analysis
荧光光谱基础; 蛋白质的荧光特性; 荧光分光光度计的结构和原理。吸收光谱和荧光光谱能级跃迁示意图 (一)荧光的产生 某些物质受紫外光或可见光照射激发后能发射出比激发光波长较长的荧光。此化学物质能从外界吸收并储存能量(如光能、化学能等)而进入激发态,当其从激发态再回复到基态时,过剩的能量可以电磁辐射的
RNA-FISH-on-cultured-cells-in-interphase2
Post-labeling DNA processing and purificationQiagen PCR clean up to get rid of unused oligonucleotides;Add 20µl cot1DNA, 10µl ssDNA to compete for rep
DAPI-Counterstaining-Protocols
实验概要The blue-fluorescent DAPI nucleic acid stain preferentially stains dsDNA; it appears to associate with AT clusters in the minor groove. Binding
Flow-Cell-Assays-with-Microtubules:-Motility/Dynamics-in-Fluorescence
Flow cell assays are very useful for studying microtubule motility, microtubule dynamics, kinetochore-microtubule interactions and action of severing/
DAPI-Nucleic-Acid-Stain
实验概要The blue-fluorescent DAPI nucleic acid stain preferentially stains dsDNA; it appears to associate with AT clusters in the minor groove. Binding
均相荧光免疫测定(homogeneous-fluorescence-immunoassay)
均相荧光免疫测定(homogeneous fluorescence immunoassay)是根据1972年Rubenstein等建立的均相酶免疫测定法(HEI)发展形成的一种新型免疫荧光分析技术。所谓“均相”是指在反应结束后无须对游离和结合的标记物进行分离,直接测定即可。均相荧光免疫测定是利用
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实验原理荧光原位杂交(Fluorescence in situ hybridization FISH)是一门新兴的分子细胞遗传学技术,是20世纪80年代末期在原有的放射性原位杂交技术的基础上发展起来的一种非放射性原位杂交技术。目前这项技术已经广泛应用于动植物基因组结构研究、染色体精细结构变异分析、病
Fluorescence-Procedures-forthe-Actin-andTubulin-Cytoskeleton-in-Fixed-Cells
Fluorescence Procedures for the Actin and Tubulin Cytoskeleton in Fixed CellsActin: Louise CramerTubulin: Arshad DesaiGeneral StrategyWe typically wor