Sectioningstainedembryos.

The protocols for plastic and wax sections as used by the Vize lab. These protocols work, but they have not been optimized. If anyone has better protocols please let us know.Samples.Stain samples strongly, remember that in a section only the very strongest stain will be visible, even quite strong background will not be visible. BCIP/NBT is the only stain we have successfully used, we have tried Red new fuschin but it......阅读全文

连续断层3D重构中的超薄切片制备

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siRNAs结合生物芯片的实验设计2

Figure 2. Silencer ™ siRNA Validation Data Generated Using Applied Biosystems TaqMan® Gene Expression Assays. The indicated Silencer Validated siRNAs

Largescale-Immunocytology

This protocol describes our method for preparing cells for immunofluorescence, in which all incubations and washes are performed in microtiter dishes.

Fast-and-reliable-miniprep-RNA-extraction-from-Neurospora-crassa

We have developed a method for isolating high quality total RNA from N. crassa mycelia that reliably yields large quantities. It is possible to extrac

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This is a four day procedure so it's best to start on Monday or Tuesday.CASE SELECTION:H&E stained thin sections are first reviewed by a pathologi

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QUALITATIVE-ANALYSIS-OF-DNA-FRAGMENTATION-BY-AGAROSE-GEL-ELECTROPHORESIS

1. IntroductionNuclear morphology changes characteristic of apoptosis appear within the cell together with a distinctive biochemical event: the endonu

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对生物样品进行快速可靠的原位成像以揭示与复杂的多细胞生物相关的动态过程一直都是光学成像的一大目标。传统的激光共聚焦显微镜虽然具有优异的3D荧光成像功能,提供了非常高的空间分辨率,但是在某些实验中,成像速度不够快和光漂白问题依然不容忽视。光片技术的提出就很好地解决了这些问题,同时还保有优异的空间分辨率

LIVE/DEAD®-Violet-Viability/Vitality-Kit

实验概要The LIVE/DEAD®  Violet Viability/Vitality Kit provides a two-color fluorescence cell  viability and vitality assay that is based on the simultaneo

Assay-of-superoxide-dismutase-activity2

Cuvette holders in the sample chamber of the spectrophotometer were thermo-controlled at 25°C. For the blank test, 100 ml of 50 mM potassium phosphate

DNA的酶学操作

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流式细胞仪技术专辑

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The development of chick embryos has been studied since Aristotle. It is one of the most intensely studied organisms. One reason for this is that ther

Column-Method-for-Lambda-Phage-DNA-Preparation

Purpose:Mini-prep method for lambda phage DNA purification from lysates.Time required:4 hours once the lysate is in handSpecial supplies required:BioR

玉米Proline-responding-1(pro1)突变在蛋白合成和细胞...(二)

Pro1基因编码一个△1-吡咯啉-5-羧酸合成酶(P5CS) 对玉米经典突变pro1基因进行图位克隆发现,玉米Pro1基因编码一个△1-吡咯啉-5-羧酸合成酶(P5CS) (Figure 2A),它是催化以谷氨酸为前体合成脯氨酸过程中的限速酶(Figure 2B, C, D, E)。Pro1基因功能

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实验概要The CellTrace™  Violet Cell Proliferation Kit provides a versatile and well-retained  cell tracing reagent in a convenient and easy-to-use form. T

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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

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The overall quality of an RNA preparation may be assessed by electrophoresis on a denaturing agarose gel; this will also give some information about R

Cloning-of-small-RNAs-with-5’-phosphate-and-3’-OH-ends01

IntroductionThe following protocol describes a procedure for the purification and cloning of miRNAs and other small RNAs in the  20-30 nucleotide size

Bromodeoxyuridine-Immunohistochemistry

Introduction: This method for the detection of cellular proliferation includes several modifications of a previously published protocol (Hayashi, et a

AD模型小鼠全脑Aβ斑块及其周围多种结构的高精度全景图

  在全脑范围同时获取多种结构的高分辨图谱,对于剖析脑功能及阿尔茨海默症(AD)等神经系统疾病的发病机制具有重要意义。当前,已有的成像技术和方法在实现大尺度、高分辨率的多种脑结构元素同步成像方面,面临挑战。  近日,中国科学院上海药物研究所MOST与图像融合技术服务部在Frontiers in Ne

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OverviewR&D Systems provides monoclonal, polyclonal and biotinylated antibodies for immunohistochemical use. The following protocol has been developed

UV-CrossLinking-an...-(二)

实验步骤1. UV cross-linking of tissue culture cells    1) Remove media and add ice-cold PBS to cells (e.g. use cells grown in a 10 cm plate for three ex