MethodsfortheMeasurementofaBacterialEnzymeActivityinCellLysates

AbstractThe kinetic characteristics and regulation of aspartate carbamoyltransferase activity were studied in lysates and cell extracts of Helicobacter pylori by three diffirent methods. Nuclear magnetic resonance spectroscopy, radioactive tracer analysis, and spectrophotometry were employed in conjunction to identify the properties of the enzyme activity and to validate the results obtained with each assay......阅读全文

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates

AbstractThe kinetic characteristics and regulation of aspartate carbamoyltransferase activity were studied in lysates and cell extracts of Helicobacte

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates4

The use of a micro-titre based colorimetric assay provided a third method for the study of ACTase activity, and the most useful for large scale measur

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates2

Measurement of ACTase activityNuclear magnetic resonance spect roscopy (NMR)The unique potential of NMR spectroscopy for monitoring simultaneously the

Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates3

Different enzyme assays for ACTase study in H. pyloriACTase properties were studied in situ in cell-free extracts to obtain information on enzyme func

Hydrolytic-Activity-of-Bacterial-Supernatants-for-Fungal-Suppression

As the fungal growth suppression by biocontrol agents (BCA) in solid media using dual plate assay has some issues regarding nutrient limitation. A pro

Histochemical-staining-of-sea-urchin-embryos-for-(AP)-enzyme-activity

Histochemical staining of sea urchin embryos for alkaline phosphatase (AP) enzyme activity1. Obtain embryo samples, tube of AP substrate buffer and tu

Bacterial-cell-culture

MaterialsGlass culture tubes with metal caps and labelsGrowth medium, from media room or customizedGlass pipette tubesParafilmEquipmentVortexerFireboy

Staining-Methods-for-cell

death Z. Xia 10/2/95The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidiu

Measurement-of-Cell-Adhesion-Under-Static-Conditions

Many different molecules have been described to promote cell adhesion including several cell surface carbohydrate-binding proteins. Measuring cell adh

Staining-Methods-for-cell-death

The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidium iodide)-red, dead

Analysis-of-Proteins-using-Small-Format-2D-Gel-Electrophoresis

Preparation of protein samplesIntracellular virus proteinsThe following method has been developed principally for the analysis of intracellular protei

Cellfree-System-for-the-examination-of-apoptotic-activity

 IntroductionIn our lab we use the term 'cell-free system' when we talk about the examination of apoptotic activity in cytoplasmic extracts. T

Adiponectin-Replenishment-Ameliorates-ObesityRelated-Hypertension(二)

Methods    Animal and Animal Treatment    KKAy male mice were purchased from Japan CLEA (Tokyo, Japan). This strain is a cross between black KK fema

Enzyme-Kinetics-assay-of-the-WT

To assay 17 b-HSD activity in lysates, cells were harvested 48h after transfection using PBS Enzyme Free Cell Dissociation Solution ( specialty Media

Guide-to-Cell-Proliferation-and-Apoptosis-Methods

Chapter 1: Cell Death - Apoptosis and Necrosis1.1Introduction21.1.1Terminology of cell death21.1.2Differences between necrosis and apoptosis31.1.3Apop

AlamarBlue®-Cell-Viability-Assay

实验概要Assess cell viability. 实验原理Cell  health can be monitored by numerous methods. Plasma membrane integrity,  DNA synthesis, DNA content, enzyme activ

E.Z.N.A.™-Fastfilter-Plasmid-Mega-Protocol

实验概要The  E.Z.N.A.™ family of products is an innovative system that radically  simplifies extraction and purification of nucleic acids from a variety  

Measurement-of-primary-endothelial-cell-permeability-to-fluxes-of-dextran..

Measurement of primary endothelial cell permeability to fluxes of dextran or albuminThe fluxes of albumin or dextran across vascular endothelial cell

Lambda(噬菌体)DNA-Miniprep

David HarryInstitute of Forest GeneticsUSDA Forest ServicePacific Southwest Research StationAugust 26, 1993Background :There are many published method

Cell-Staining-for-SenescenceAssociated-betaGalactosidase--Activity

DescriptionCell Staining for Senescence-Associated â-Galactosidase (SA-â-Gal) Activity Procedure1. Carefully remove the growth media from the cell cul

Combined-Flow-Cytometric-Measurement-of-Two-CellSurface-Antigens

INTRODUCTIONFlow cytometry is frequently used to assess nucleic acid content in individual cells. Based on DNA content alone, however, cells in the qu

Western-杂交

Western 杂交(主要内容如下)Preparing of Protein LysatesWestern BlottingFar Western BlottingSemi Dry BlottingStripping MembranesTrouble Shooting and OthersPrepa

DNA转染

DNA转染·         Transfection of Mammalian Cells Using Lipofectamine (LTI)·         Guide to Eukaryotic Transfections with Cationic Lipid Reagents (PDF)

Tissue-Culture-Methods2

IV. MAINTENANCECultures should be examined daily, observing the morphology, the color of the medium and the density of the cells. A tissue culture log

Cell-and-tissue-lysis-hub

This page should point you to the many different general and lab-specific protocols describing tissue and cell lysis and serve as forum for comparison

Embryo-Lysates--Immunoprecipitation

Embryo lysatesTake 25 embryos and place into 1.7ml centrifuge tube.Rinse once in lysis buffer (add ~ 1ml) and remove by aspirationAdd 500 µL lysis buf

Yeast-Lysates-for-Westerns

Cells are grown for 2-3 days as 1.5ml prep. under selection for the plasmid of interest. Spin cells down 2.6K for 5min.Resuspend in 1ml 0.25m NaOH/1%

Preparation-of-Phage-Lysates

Preparation of Phage LysatesInoculate 5 ml of lambda-broth in a glass culture tube with a single colony of an appropriate host strain of E. coli. Incu

Combined-Flow-Cytometric-Measurement-of-Two-CellSurface-Antigens2

DNA and RNA Staining6. Stain cells with 7-AAD: i. Resuspend the cells from Step 5 in 0.5 mL of NASS containing 10 µg/mL of 7-AAD. Incubatefor 20 min a

Bacterial-transformation

IntroductionTransformation is the process of introducing foreign DNA (e.g plasmids, BAC) into a bacterium. Bacterial cells into which foreign DNA can