ProtocolsforLCMpreparationandanalysis

Protocols for LCM preparation and analysis I. Preparation, LCM and RNA/DNA extraction of Frozen Tissue SectionsA. EmbeddingB. CuttingC. StainingII. Preparation and LCM of Paraffin Embedded Tissue SectionsFor both I & II Frozen & Paraffin-EmbeddedTissue SectionsD. Laser TransferE. DNA Extraction Protocol of LCM tissue and PCR for DNA analysisF. RNA Extraction Protocol of LCM ......阅读全文

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

porcine-brain-tubulin-prep

Although many protocols for tubulin preparation are available, the procedure described below is the simplest and highest yielding preparation I have d

CDNA文库

 CDNA文库(主要内容如下)·         Construction of cDNA Library·         Construction of Genome DNA Library·         Library Screening  OthersConstruction of cD

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

Preparation-of-Rat-Liver-Cell-Cytosol

These protocols should yield enough cytosol and organelles for 1-200 MT/Organelle motility assays.Solutions and Reagents  Freshly removed or flash fro

Preparation-of-Agarose-Gels-for-DNA-separations

Weigh out the desired amount of agarose and place in an Erlenmeyer flask with a measured amount of electrophoresis buffer, e.g. for an 0.8% gel, add 0

Preparation-of-Segmented-and-Polarity-Marked-Microtubules

Segmented and polarity-marked microtubules are very useful for many different types of in vitro assays. Segmented microtubules are microtubules with a

Preparation-of-Mitochondria-from-Rat-Liver

Preparation of Mitochondria from Rat LiverRat liver is an ideal source for functional intact mitochondria for a number of reasons. We use Sprague-Dawl

Preparation-of-Segmented-and-Polarity-Marked-Microtubules

Preparation of Segmented and Polarity Marked Microtubules Segmented and polarity-marked microtubules are very useful for many different types of in vi

Specimen-Preparation-for-Scanning-Electron-Microscopy

Specimen Preparation for Scanning Electron MicroscopyWe recommend consultation with one of the lab directors before preparing specimens. The methods p

Slice-and-Explant-Culture-Protocols-–-Hevner-lab-2002

for axon tracing & cell culture studies in vitro using embyros age E11.5 – E16.5modified from Rubenstein lab and Price lab protocols1. Setupa. 2 hr be

Assessment-of-Magnaporthe-grisea-mating-type-by-spore-PCR

Isolation of DNA from filamentous fungi for PCR analysis is usually time consuming and involves use of toxic chemicals such as phenol/chloroform. In S

Lipid-analysis:EXTRACTION-OF-LIPIDS-FROM-LIPOPHORIN

Lipid analysisEXTRACTION OF LIPIDS FROM LIPOPHORIN Since lipids are hydrophobic, they are better soluble in organic solvents than in water. Because th

FIXATION-and-DNA-Staining-for-Cell-Cycle-Analysis

BackgroundThis method of DNA staining utilizes ethanol to fix the cells and permeabilize the membrane, which allows the dye (Propidium Iodide) to ente

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

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

Whole-mount-TUNEL-analysis-of-Xenopus-embryos

Fixation and pretreatmentDejelly albino embryos carefully in 2% Cystein (pH 7.8).Remove the vitellin membrane with two pairs of tweezers         (or c

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

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

Flow-Cytometric-Analysis-Of-Bcl-Family-members

DescriptionCell Fixation, staining and flow cytometric analysis ProcedureCells (106) were washed twice in FACS buffer (phosphate buffered saline PBS p

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

引物延伸分析(primer-extension-analysis)

引物延伸分析(primer extension analysis)主要用于mRNA 5′端作图。poly(A)+RNA首先与过量5′端标记的且与靶RNA互补的单链寡核苷酸引物杂交,然后用反转录酶延伸这个引物。产生的cDNA与RNA模板互补且长度与引物5′端和RNA 5′端之间的距离相等。该法在mRN

引物延伸分析(primer-extension-analysis)

引物延伸分析(primer extension analysis)主要用于mRNA 5′端作图。poly(A)+RNA首先与过量5′端标记的且与靶RNA互补的单链寡核苷酸引物杂交,然后用反转录酶延伸这个引物。产生的cDNA与RNA模板互补且长度与引物5′端和RNA 5′端之间的距离相等。该法在mR

细胞遗传学——原位杂交(ISH)

In Situ Hybridization·         In Situ Hybridization (jsmith1@po-box.mcgill.ca)In situ hybridization, as the name suggests, is a method of localizing,

Agilent发布改变游戏规则的Encore-Multispan液体处理系统

  Agilent科技公司已经发布了Encore Multispan液体处理系统,将一系列独特技术整合其中。不同于目前的任何仪器,将用全新的自动化功能改善研究过程的每一阶段。  Agilent Introduces the Encore Multispan Liquid Handling Syste

Intestinal-intraepithelial-lymphocytes

Intestinal intraepithelial lymphocytes    Intestinal intraepithelial lymphocytes (IELs) are mostly T cells, which are continuously associated with gut

定量RTPCR-(Quantitative-RTPCR)

Application: Quantitative RT-PCR is used to quantify mRNA in both relative and absolute terms. It can be applied for the quantification of mRNA expres

Multicolour-3DFISH-in-vertebrate-cells1

IntroductionMulticolour 3D-FISH in combination with confocal microscopy, 3D image reconstruction and quantitative image analysis is an efficient tool