LiveCellImagingofYeast
Live Cell Imaging of YeastDaniel R. Rines, Dominik Thomann, Jonas F. Dorn, Paul Goodwin and Peter K. SorgerINTRODUCTIONThe development of cloning vectors for green fluorescent protein (GFP) and the simplicity of yeast reverse genetics allow straightforward labeling of yeast proteins in living cells. Budding and fission yeast are therefore attractive organisms in which to study dynamic cellular processes such as growt......阅读全文
LIVE/DEAD®－Violet－Viability/Vitality－Kit
实验概要The LIVE/DEAD® Violet Viability/Vitality Kit provides a two-color fluorescence cell viability and vitality assay that is based on the simultane
Yeast－Genomic－DNA－Prep
Grow 10ml YPD cultures o/n. Figure out cell density; inoculate 30 ml YPD and grow o/n so that cell density is approximately 2 x 108cells/ml the next m
Endy:Yeast－Colony－PCR
MethodUsing sterile pipette tips, transfer a 1 mm colony into 50 uL of 60 U/ml Zymolyase3 uL of 1 U/mL Zymolyase stock solution47 uL of waterIncubate
Decontamination－of－cells－from－the－yeast
I Destroy yeast1. Aspirate medium and wash cell in PBS.2. Incubate cells at 37oC for 5 min in non-diluted antibiotic-antimycotic.3. In
Blackburn:Yeast－Colony－PCR
OverviewThis is a quick and easy yeast colony PCR protocol that does not require zymolyase step.Updated Protocol: Blackburn Lab: Quick and Easy Yeast
Plasmid－isolation－from－yeast
Pick colonies into 0.5ml of SD-Leu (or other appropriate SD medium)Vortex for 1minLeave to grow O/N for 18-24h at 30°C, 230-250rpm (best in 5ml bijou)
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
布鲁克宣布收购ACQUIFER－Imaging－GmbH
2023年1月5日，布鲁克公司（纳斯达克股票代码：BRKR）宣布收购 ACQUIFER Imaging GmbH，该公司是生物成像和高内涵显微镜大数据管理解决方案的先驱。此次收购增加了高性能的本地处理、安全存储和网络技术，补充了布鲁克先进的荧光显微镜成像产品，如可生成高信息内容的光片和超分辨
布鲁克：新品云游ASMS－2020
分析测试百科网讯 近日，布鲁克对外宣布其在ASNS 2020期间的会议日程： Sunday, May 31, 2020, 8:30 am – 12:00 pm CDT 演讲嘉宾： 《What‘s New with Bruker》 Rohan Thakur, PhD, Managing D
Live－Lab创新展区－2020－回顾
“安全、智慧、可持续”是labtech China Congress三大核心词，大会配套的产品及技术诠释了这三个关键词。现场实验室Live Lab和创新展区结合，汇聚实验室仪器、设备与耗材、实验室家具与建设等行业新产品与新技术，通过场景化演示、操作及演讲，科学高效的管理模式，实验室现代化设计风格
Acid－Phenol－Yeast－RNA－Prep
This is the preferred method for yeast RNA preparationuse Gloves and RNAse free solutions throughout.1. Use a YPD overnight culture to innoculate fres
IMAGINGPAM相关文献集（四）
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德国WALZ公司生产的M系列调制叶绿素荧光成像系统IMAGING-PAM，作为全球最权威的叶绿素荧光成像系统，在国际科研界得到了广泛应用，已经成为叶绿素荧光成像研究的行业标准。 泽泉科技有限公司作为德国WALZ在中国的技术服务中心，一直以来致力于推广调制叶绿素荧光技术在国内科研界的应用，并
细胞组分和细胞器——细胞骨架
Fixation and Immunofluorescence of the Cytoskeleton (Mitchison Lab) Recycling Tubulin (Mitchison Lab) Labeling Tubulin and Quantifying Labeling Stoi
Preparation－of－Yeast－DNA－Embedded－in－Agarose－Plugs
Preparation of Yeast DNA Embedded in Agarose PlugsAnja van Brabant(adapted from Iadonato, S. P., and A. Gnirke. 1996. RARE-cleavage analysis of YACs.
Sucrose－Density－Gradient－Fractionation－of－Yeast－Membranes
Grow a 2 ml culture, 24 hr. at 30oC in selective mediaWhen culture is ready, use it to inoculate about 55 ml (50 ml plus 5 for O.D.600 readings) of se
Yeast－Gene－knockout－using－Oligo/PCR
Universal primers for gene knock-out using dominant drug markers: Kan, Clonat, and Hygromisin-B. Forward primer: 5’ TCAGGGGCATGATGTGACT 3’Reverse prim
通过细胞受体代谢生物素化进行图像分析
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Alexa－Fluor®－488－Annexin－V/Dead－Cell－Apoptosis－Kit
实验概要Apoptosis is a carefully regulated process of cell death that occurs as a normal part of development. Inappropriately regulated apoptosis is imp
Silver:－TimeLapse－Microscopy
Pad Preparation1. Microwave 2% agarose (mix of low-melt and normal, to taste) in Thorn media (see below). (If you have used different percentages of a
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7月21日，发表在Science上的一项研究中，科学家们发表了关于染色体追踪的一项重要成果。哈佛大学庄小威教授以及哈佛医学院Chao-ting Wu 教授是本文的共同通讯作者。 染色质的空间组织从很大程度上影响着基因组的功能。最近，科学家们通过染色体-构象-捕捉揭示了间期染色体大量的结构信息，
Snf1－in－Yeast－Glucose－Repression/Derepression
The Snf1 protein kinase is a central component of the signalling pathway for glucose repression in yeast. On removal of glucose, gene repression is re
Quick－and－Easy－Isolation－of－Genomic－DNA－from－Yeast
ProcedureTransfer 1.5 ml of liquid culture of yeast grown for 20 - 24 h at 30°C in YPD (1% yeast extract, 2% peptone, 2% dextrose) into a microcentrif
Rgt1－in－Yeast－Glucose－Induction－Pathway
Yeast sense glucose in their environment and alter gene expression to match their nutritional needs. In a glucose-rich environment, glycolysis is acti
High－Molecular－Weight－Yeast－Liquid－DNA－Preparation
Purpose:To isolate intact, high molecular weight DNA from yeast cells for subcloning and rare cutting restriction enzyme analysis. One can expect a yi
Method:－Removal－of－Yeast－Contamination－from－Lymphoblast－Cultures
Purpose:This method is advantageous for saving the occasional cultures that become contaminated. Yeast contaminated cultures will appear cloudy when s
A－Yeast－Secretion－Trap－Assay－for－Identification－of－Secreted－Proteins－...
Secreted proteins from plants and phytopathogens play important roles in their interactions and contribute to elaborate mechanisms of attack, defe