StreakingBacterialStocks

Principle:Bacterial cells are streaked onto a medium to obtain an independent isolate. This is done to reduce the likelihood of working with a culture which has become contaminated and/or has accumulated mutations.Time Required:Less than 5 minutes to streak out each strain; the colonies grow overnight.Procedure:The cells can be streaked from another plate a stab or from a frozen glycerol stock. Pick up a slightly vis......阅读全文

Streaking-Bacterial-Stocks

Principle:Bacterial cells are streaked onto a medium to obtain an independent isolate. This is done to reduce the likelihood of working with a culture

Bacterial-glycerol-stocks

To 2mls of mid-log culture or 1ml of freshly saturated culture add 1 ml(or an equal volume) of glycerol solution, mix gently, then freeze rapidly in l

Bacterial-Media-Solutions-and-Stocks

3 agar (200 ml)Add 6 grams agar to 200 ml deionized water. Autoclave to sterilize.1.6 agar (200 ml)Add 3.2 grams agar to 200 ml deionized water.Autocl

细菌培养

Preparing Overnight Bacteria Culture (LaboratoryExperiments.com)This is a basic procedure for high school students and useful for those who are new to

Streaking-Bacteria-for-Single-Colonies

1. Initial inoculum:- From solid media, touch an isolated colonies with a sterile applicator or toothpick.- From liquid media, touch the culture with

酵母培养

Streaking Yeast Stocks (Donis Keller Lab)Very nice protoocol for yeast workLong-Term Storage of Yeast Stocks (Donis Keller Lab)Yeast storage and reviv

Bacterial-transformation

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

Yeast-Media,-Solutions-and-Stocks

Yeast Media:Note: Synthetic complete medium can be prepared by adding media supplements (see below).Medium using 6.7 g yeast nitrogen base without ami

XC-Assay-of-MoMLV-Virus-Stocks

MaterialsWildtype MoMLV virus aliquot.  Stored at -80ºC.Medium:  DMEM + 10% FBSNIH 3T3 TK- cellsXC cellsPolybrene 1000x stock = 4 mg/mL, sterile filte

Bacterial-Colony-PCR

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

Bacterial-cell-culture

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

Preparing-Overnight-Bacterial-Culture

Materials:Sterile LB medium (Luria-Bertani Medium) with or without antibiotic:water 500 mlbacto-tryptone 10 gbacto-yeast extracts 5 gsodium chloride 1

Long-Term-Storage-of-Bacterial-Strains

Purpose:Bacterial strains may be stored indefinitely at low temperatures (- 20 degrees C and -80 degrees C) in 15 to 40 glycerol. It is lab policy to

Bacterial-Expression-of-GSTfusion-Proteins

1.  Grow cells in 5ml (or more) of LB-Amp overnight for a starter culture. 2.  Grow larger culture (100x volume of starter culture) using the overnigh

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

细菌培养基

Preparation of LB Plate (Dr. Chastain)prepare LB plate with or without antibioticsBacterial Culture Media Recipes (WUGSC) M9 Plate Supplement (Gottsch

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

细菌转化(bacterial-transformation)原理和操作

1.目的学会质粒DNA转化感受态受体菌的技术。2.原理质粒DNA粘附在细菌细胞表面,经过42°C短时间的热击处理,促进吸收DNA。然后在非选择培养基中培养一代,待质粒上所带的抗菌素基因表达,就可以在含抗菌素的培养基中生长。3.器材旋涡混合器,微量移液取样器,移液器吸头,1.5ml 微量离心管,双面微

TritonPrep-Method-for-bacterial-DNA-Purification

Triton-Prep Method for bacterial DNA PurificationGrow 5 ( large scale-15ml culture). Harvest in single eppendorf tube (or 15 ml disposable tube).Resus

Construction-and-Manipulation-of-LargeInsert-Bacterial-Clone-Libraries

Acknowledgements The organizer of the workshop acknowledges Dr. Murray Milford, Professor and Interim Head, and Dr. Mark Hussey, Professor and Interim

Preparation-of-Bacterial-Proteins-for-Analysis-by-2DPAGE

The following protocol has been developed for preparing soluble bacterial proteins in a form suitable for analysis by 2D-PAGE. The procedure was princ

Production-of-Antibody-Fragments-in-Arabidopsis-Seeds

Plants offer a number of attractive benefits over conventional mammalian or bacterial cell culture systems for the production of valuable pharmace

Basic-Methods-of-Culturing-Drosophila

实验概要Basic Methods of Culturing Drosophila实验步骤Stockkeeping1. Mechanics        Most stocks can be successfully cultured by periodic mass transfer of a

Screening-Bacterial-Colonies-Using-Xgal-and-IPTG:-αComplementation

实验概要        α-complementation occurs when two inactive fragments of E. coli β-galactosidase associate to form a functional enzyme. Many plasmid

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-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-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

Bacterial-Expression-of-IRS1-containing-GSTfusion-Proteins

1.  Grow cells in 5ml (or more) of LB-Amp overnight for a starter culture. 2.  Grow larger culture using the overnight culture as a seeding culture. 

DNA转化

DNA转化Chemical Transformation·         Transformation of Competent Cells (RbCl2 Method) (Goldberg Lab)Very nice protocol for E. Coli transformation inc

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