HowtoprepareMolecularBiologygradeglycogen

OverviewGlycogen can conveniently substitute for tRNA as a carrier for nucleic acid precipitation. Although Molecular Biology grade glycogen can be purchased from a number of vendors, the main disadvantage is that it is very expensive (e.g., About 100 dollars/20-40 mg).Here we present a simple and inexpensive protocol to prepare a large amount of glycogen which is suitable for any kind of Molecular Biology......阅读全文

Cellular--Molecular-Pathology-Branch

VisionTo provide scientific collaboration of excellence to National Toxicology Program (NTP) (http://ntp.niehs.nih.gov/) interdisciplinary research pr

亲和层析实验技术方法

INTRODUCTIONThis protocol describes a method for removing antibodies that react with bacterially encoded proteins by passing a crude preparation of im

How-to-make-DEPCtreated-water-and-Tris-Buffer

Add 0.1 ml DEPC to 100 ml of the solution to be treated and shake vigorously to bring the DEPC into solution.Let the solution incubate for 12 hours at

How-to-use-Basic-Local-Alignment-Search-Tool-(BLAST)

DescriptionThe BLAST algorithm was developed as a way to perform DNA and protein sequence similarity searches by an algorithm that is faster than FAST

How-do-I-decontaminate-my-tissue-culture-(Invitrogen)

When an irreplaceable culture becomes contaminated, researchers may attempt to eliminate or control the contamination. First, determine if the contami

New-white-paper-explains-how-to-increase-brewing-process-……

Ensuring production processes will operate as necessary and generate the desired product quality and yield in the required time is central to succ

How-to-perform-automated-counts-of-fluorescently-stained-cells.

NoteThis protocol describes semi-automated cell counts using fluorescently labeled cells, a hemocytometer and ImageJ software.  The hemocytometer is n

Assay-for-the-Micrococcal-Nuclease

Method: Essentially that described by Heins et al. (1966) based upon the release of acid soluble oligonucleotides following nuclease digestion of DNA.

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

2%多聚甲醛固定剂配方二则

METHOD 1:Formaldehyde preservative – 2% formaldehyde solution in protein-free phosphate-buffered saline (PBS).Prepare as follows:Add 2 g paraformaldeh

PREPARATION-OF-2%-FORMALDEHYDE-STOCK-SOLUTION-(2-METHODS)

METHOD 1:Formaldehyde preservative – 2% formaldehyde solution in protein-free phosphate-buffered saline (PBS).Prepare as follows:Add 2 g paraformaldeh

Fluidigm公司微液流芯片在单细胞研究中的应用(一)

Nature杂志在2009年5月7日的主页文章中大篇幅地介绍了美国Fluidigm公司的微液流芯片在单细胞表达中的应用。A closer look at the single cellMegan ScudellariNature Reports Stem CellsPublished online:

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

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,

Chemical-Genomics-Approaches-in-Plant-Biology

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实验室自动化与筛选协会2013亚洲会展展商技术论坛

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How-to-Import-Medline-Search-Result-(DUMC-OVID)-in-Reference-Manager

If you would like to print this page, please use the printer inRm. 221 since printing through those printers in the computer rooms will be UNBELIEVABL

其它PCR方法

·         Standard PCR Protocol (Molecular Biology Techniques Manual)The followings are described in detailRecommended Reagent ConcentrationsRecommend

Bradford-protein-assay

Bradford protein assayConsiderations for useThe Bradford assay is very fast and uses about the same amount of protein as the Lowry assay. It is fairly

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Plants belonging to the Rhododendron subgenera Pentanthera (deciduous) and Tsutsusi and Azaleastrum (evergreen) are called azaleas. Concerning their m

分子克隆(molecular-coloning)常用技术

一、核酸的纯化在分子克隆 的所有操作中,最基本的操作是核酸的纯化。其关键步骤是去蛋白质,通常只要用酚/氯仿。氯仿抽提核酸的溶液即可。每当需要把克隆 有某一些所用的酶灭活或去除以便进行下一步时,可进行这种抽提。然而,如要从细胞裂解液等复杂的分子混合物中纯化核酸,则要先用某些蛋白水解酶消化大部分蛋白

Bacterial-Colony-PCR

Bacterial Colony PCRObjective:This protocol allows rapid detection of transformation success when primers are available to allow determination of corr

Polyphenoloxidase-(catechol-oxidases)-assay

Browning of the cut surface of some fruits and vegetables is due the presence of a group of enzymes called polyphenoloxidases. These enzymes are relea

Organelle-DNA-Library-Construction

Organelle DNA Library Construction(version MAY-1998)I. NEBULIZATION of DNA      1. 0.5 - 5 ug DNA in TE (10mM/1mM), 25% glycerol, final volume 500 ul

Preparing-Lambda-DNA

Preparing Lambda DNA1- Coliphage lambda DNA is a widely used vector for recombinant DNA. The middle third of its 48,000 bp contains no genes required

2D-Polyacrylamide-Gel-Electrophoresis

This method was successful in our lab using prostate tissue and for our specific objectives. Investigators must be aware that they will need to tailor

PCR产物纯化方法

Purification of PCR Products in Preparation for CloningJoseph SambrookPeter Maccallum Cancer Institute and The University of Melbourne, AustraliaDavid

Transformation-Protocol-for-Arabidopsis

Transformation Protocol for Arabidopsis – AbbreviatedGerminate seed in pots↓ 4 weeksStreak bacteria onto YM/MinA↓ 2-3 days 28°CSpray/dip bacterial sus

Microarrays-to-Characterize-the-MolecularGenetic-Basis-of-Disease

article by Dr. RL McInnes, Agilent Technologies, AustraliaGenomic instability underlies cancer and Copy Number Aberrations (CNA s) are known to underp

Restriction-Digests-of-High-Molecular-Weight-Yeast-DNA

Purpose:To perform restriction digests of YACs for mapping using rare cutting enzymes or more conventional restriction endonuclease digestion.Time req