SpecimenPreparationforScanningElectronMicroscopy

Specimen Preparation for Scanning Electron MicroscopyWe recommend consultation with one of the lab directors before preparing specimens. The methods presented here provide an overview of preparation techniques for a variety of specimens.Conductive Specimens (such as metallic objects):Usually, these specimens do not have to be sputter coated. Simply mount the specimen on a SEM stub using conductive paint or putty......阅读全文

分析仪器中英文名称对照

仪器中文名称      仪器英文名称             英文缩写 原子发射光谱仪     Atomic Emission Spectrometer        AES   电感偶合等离子体发射光谱仪 Inductive Coupled Plasma Emission Spectrometer

Sample-preparation-(analytical-gels)

Sample preparation and solubilization are crucial factors for the overall performance of the 2-D PAGE technique. Protein complexes and aggregates shou

Easy-YAC-Preparation-Method

YAC TRANSFORMATION OF C. ELEGANS USING TOTAL YEAST GENOMIC DNA[This method is described in The Worm Breeder's Gazette (1997) A. Davies and J. Shaw

Preparation-of-Sonicated-Human-DNA

Purpose:To break up high molecular weight human placental DNA into fragment sizes of 500 bp or less which can be used as competitor DNA in Southern an

Protocols-for-LCM-preparation-and-analysis

Protocols for LCM preparation and analysis I. Preparation, LCM and RNA/DNA extraction of Frozen Tissue SectionsA. EmbeddingB. CuttingC. StainingII. Pr

Preparation-of-tubulin2

DAY 2: Cycling preparation of MT protein.Keep the brains in an evacuated plastic ziplock bag buried in ice from the time of slaughter during transport

Tissue-preparation-protocol-for-ChIP

实验概要This protocol  describes how chromatin is prepared from tissue, which can subsequently  be used for chromatin immunoprecipitation (ChIP). It is re

Midiprep-preparation-of-Plasmid-DNA

实验概要The  PureLink™ HiPure Plasmid DNA Midiprep Kit allows purification of  100–350 μg of high-quality plasmid DNA from 15–25 mL overnight E. coli  cul

Large-Scale-Tubulin-Preparation

Tubulin is purified from bovine/porcine brain by two cycles of polymerization/depolymerization followed by removal of copurifying proteins on a phosph

Preparation-of-Lactobacillus-Competent-Cells

OverviewInstructions on how to prepare Lactobacillus plantarum competent cells before electrotransformation.MaterialsMRS mediaCulture of L. plantarum 

Preparation-of-nucleic-acid-probes

Preparation of nucleic acid probesIn standard nucleic acid hybridization assays the probe is labeled in some way. Nucleic acid probes may be made as s

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

Maxiprep-preparation-of-Plasmid-DNA

实验概要The  PureLink™ HiPure Plasmid DNA Maxiprep Kit allows purification of  500–850 μg of high-quality plasmid DNA from 100–200 mL overnight E. coli cu

Preparation-and-Staining-of-Paraffin-Sections

I. Fixation and Processing of Tissue for Paraffin SectionsA. Fixation of Tissues in 10% Neutral Buffered FormalinSacrifice animal by prescribed and ap

光合电子传递-(photosynthetic-electron-transport)

光合作用中,受光激发推动的电子从 H2 O到辅酶Ⅱ( NADP )的传递过程。光合色素吸收光能后,把能量聚集到反应中心——一种特殊状态的叶绿素 a分子,引起电荷分离和光化学反应。一方面将水氧化,放出氧气;另一方面把电子传递给辅酶Ⅱ( NADP ),将它还原成 NADPH,其间经过一系列中间(电

EBSD分析(electron-backscatter-diffraction)是指

EBSD即电子背散射衍射。EBSD的原理始于20世纪50年代,技术问世于80年代。EBSD是扫描电子显微镜(SEM)的一个标准分析附件,但大大拓宽了扫描电子显微镜进行微观分析的功能。它可以与SEM的其他功能(包括EDS等配件)结合起来,原位成像、成分分析、大样品分析、粗糙表面成像等,克服了传统分析方

SCI论文中怎样描述TEM结果?样品有怎样的形貌

鉴于有同学问我对于SCI论文写作这个部分的更新计划,我在这里稍微跟大家说一下。这个部分肯定不仅仅是列出一些常规实验结果如何描述这么简单。现在发的这些呢,只是一些基础准备。在将这些准备工作做完了之后,我们会按照论文的结构,对每个部分进行详细讨论,尽可能把我们这些年学到的有用的东西分享给大家,给大家提供

Brain-Synaptosomal-...

实验概要The protocol provides a method of brain synaptosomal preparation.主要试剂 1. 2.55 M sucrose (unbuffered)    1) Heat on a stirring block to dissolve, t

Measurement-of-GFP-Expression-and-DNA-Content-in-Permeabilized-Cells

ReagentsCells to be studied expressing green fluorescent protein (GFP). Note that the same cell type without GFP is needed as a control.1 X PBS2% Buff

材料形貌分析

相貌分析的主要内容是分析材料的几何形貌,材料的颗粒度,及颗粒度的分布以及形貌微区的成份和物相结构等方面。形貌分析方法主要有:光学显微镜(Opticalmicroscopy,OM)、扫描电子显微镜(Scanningelectron microscopy, SEM)、透射电子显微镜(Transmis

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

A-semipermanent-mounting-medium-for-immunofluorescence-microscopy

A semi-permanent mounting medium for immunofluorescence microscopyMaterials6gm glycerol2.4gm mowiol6ml distilled water12ml Tris buffer 0.2M at pH 8.5M

原子力显微镜探针的显微镜由来

       原子力显微镜(atomic force microscope, AFM)是一种具有原子分辨率的表面形貌、电磁性能分析的重要仪器。1981年,STM(scanning tunneling microscopy, 扫描隧道显微镜)由IBM-Zurich 的Binnig and Rohrer

3-Color-Staining:-AlphaCatenin-in-HeLa-Human-Cervical-Cancer-Cells

实验概要Alpha-catenin  in HeLa human cervical cancer cells was labeled using mouse  anti-α-catenin and visualized with Alexa Fluor® 488 goat anti-mouse Ig

细胞组分和细胞器——细胞器分离

Labeling Microtubules (Molecular Dynamics Inc.  )Microtubules are involved in many aspects of cell motion including propulsion, mitosis, growth, and o

表界面科学最新文献KSV-NIMA

1.    Name:Tuning structure and properties of ultra-low cross-linked temperature-sensitive microgels at interfaces via the adsorption pathwaysAuth

电子探针仪与扫描电镜有何异同

  透射电子显微镜 (transmission electron microscopy﹐简写为TEM)。  构造原理 :  电子显微镜的构造原理与光学显微镜相似﹐主要由照明系统和成像系统构成(图1 光学显微镜与电子显微镜的对比 )。照明系统包括电子枪和聚光镜。钨丝在真空中加热并在电场的作用下发射出电

Preparation-and-Staining-of-Frozen-Tissue-Sections

I. Preparation of Frozen Sections for SectioningMaterials neeed:2-methylbutane (isopentane)Liquid NitrogenDry icePeel-Away?/sup> base moldsFrozen tiss

Preparation-of-Broth-and-Plates,-etc.

Recipes: 1) LB BrothMake 16 gm of LB Broth Base (Gibco #M27800C) up to 800 ml in ddH2O. Swirl to dissolve, then add 110 µl of 10 N NaOH.  Autoclave. 2

Large-Scale-Tubulin-Preparation——2

III. Pouring a 1L Phosphocellulose (PC) ColumnResin: Whatman P11 Cellulose Phosphate -- fibrous cation exchanger(1 gram of PC swells to about 4 ml pac