ExpressionLibraryScreening(Procaryotic)UsingAPFusionProteins
Outline:Bacteriophage lambda is a linear double stranded DNA, approximately 50 kB in size. The two sticky ends help the phage to recircularize after entering the bacterial host cell. A cDNA library is a representation of mRNA's that are expressed in a certain tissue at a certain time (e.g. rat d9 pseudopregnant decidua). Each phage contains one cDNA that was 'grabbed' by the poly-A tail and cloned into a ......阅读全文
Protein－Immunolocalization－in－Maize－Tissues
The analysis of gene expression at transcript and at protein level is of outstanding importance in plant developmental biology. Proteins can be loc
Microaspiration－of－Esophageal－Gland－Cells－and－cDNA－Library－Construction－for
Microaspiration of Esophageal Gland Cells and cDNA Library Construction for Identifying Parasitism Genes of Plant-Parasitic NematodesIdentifying p
siRNA－Design－Guidelines
Using siRNA for gene silencing is a rapidly evolving tool in molecular biology. There are several methods for preparing siRNA, such as chemical synthe
Interleukin6－Induced－Acute－Phenotypic－Microenvironment－Promote...（八）
In summary, we suggested that “acute” response could elicit innate and Th1 adaptive immunity, reversing the tumor-mediated immunosuppressive envi
Differential－cDNA－Screening－Procedures
Differential cDNA Screening ProceduresThe protocols listed refer to cDNA library construction and preliminary differential screening procedures. They
Purification－of－MBP－(maLTosebinding－proteins)－Fused－Proteins
Express fusion proteins as per the GST-fused protocol up to Step 7 (Day 3). All steps in protein purification should be done at 4° C unless otherwise
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
How－to－build－a－BAC－library
Introduction The most important aspect of our cloning vectors is that they are based on the E. coli F-factor replicon. It allows for strict
Using－GenBank
GenBank(R) is a comprehensive database of publicly available DNA sequences for more than 205,000 named organisms and for more than 60,000 within t
Interleukin6－Induced－Acute－Phenotypic－Microenvironment－Promote...（六）
Cryo-thermal therapy induced an “acute” phase response First, we performed PRM analysis upon significant proteins involved in acute phase response,
基于epMotion－5075t及KAPA文库定量试剂盒的全自动NGS文库...1
基于epMotion 5075t及KAPA文库定量试剂盒的全自动NGS文库定量操作Automated KAPA® Library Quantifcation Kit with the epMotion® 5075tMaud Brasseur¹, Jennifer Pavlica², Marsha M
实验室自动化与筛选协会2013亚洲会展短期培训课程简介
短期培训课程I ：生物制剂研发中的高通量筛选 Junma Zhou，博士，上海药明康德新药开发有限公司 刘洁颖博士，上海药明康德新药开发有限公司 In Scope of Short Course - Overview of high-throughput techniques in
Chloroplast－Phenomics:－Systematic－Phenotypic－Screening－of－Chloroplast－...
Chloroplast Phenomics: Systematic Phenotypic Screening of Chloroplast Protein Mutants in Arabidopsis As part of a project to analyze chloroplast fun
基因可隆的方法
Serial Analysis of Gene Expression (SAGE) SAGE is a powerful tool that allows the analysis of overall gene expression patterns with digital analys
Fragment－Complementation－and－Coimmunoprecipitation－Assays－for－...
Plant disease resistance (R) proteins confer protection against specific pathogens or pathogen isolates. R proteins function by recognizing patho
DNA克隆
DNA克隆（主要内容如下）· General Procedure· PCR Cloning· Subcloning· ET Cloning· Vector Preparation· Ligation Re
Establishment－of－Stable－Transfectant－of－CHO－Lec－Cells
Purpose and BackgroundsCHO lec 3.2.8.1 cellsCHO Lec 3.2.8.1 cells have four independent mutations in the N- and O- glycosylation pathways (Stanley, 19
Using－a－Counting－Chamber
Using a Counting ChamberFor microbiology, cell culture, and many applications that require use of suspensions of cells it is necessary to determine ce
Multiple－studies－with－a－single－experiment:－The－Power－of－－...（一）
Multiple studies with a single experiment: The Power of Quantitative MultiplexingMultiple studies with a single experiment: The Power of Quantitative
Purification－of－GST－Fused－Proteins
Day 1Set up an overnight culture in 100 ml LMM broth or 100 ml terrific broth containing 100ul 100 mg/mlAmpDay 2Add 40-50 ml o/n culture to 1 lt terri
Synaptic－Proteins－at－the－Synaptic－Junction
The postsynaptic density (PSD) is a submembranous structure at the postsynaptic membrane mainly at the excitatory synapses. The neurotransmitter recep
Construction－of－BAC－Libraries：Construction－of－a－BAC－library
Once high molecular weight (HMW) DNA has been prepared it must somehow be fragmented and DNA in the desired size range isolated. In general, as the de
GST融合蛋白的准备
Preparation of Glutathione-S-Transferase (GST) Fusion ProteinsMargret B. Einarson and Elena N. Pugacheva Foxx Chase Cancer Center, Philadelphia, PA 19
DNA转化
DNA转化Chemical Transformation· Transformation of Competent Cells (RbCl2 Method) (Goldberg Lab)Very nice protocol for E. Coli transformation inc
蛋白芯片制作与应用（3）－操作流程
一个经典的蛋白芯片操作流程：Experimental Procedures for Protein Microarrays--------------------------------------------------------------------------------Chemicall
FZD10基因编码功能及结构描述
这个基因是卷毛基因家族的一员该家族成员编码7-跨膜结构域蛋白，它们是无翅型MMTV整合位点信号蛋白家族的受体大多数皱褶受体与β-连环蛋白典型信号通路偶联。利用阵列分析，这一无内含子基因在两例原发性结肠癌中的表达显著上调。[由RefSeq提供，2008年7月]This gene is a member
FZD10基因突变与药物因子介绍
这个基因是卷毛基因家族的一员该家族成员编码7-跨膜结构域蛋白，它们是无翅型MMTV整合位点信号蛋白家族的受体大多数皱褶受体与β-连环蛋白典型信号通路偶联。利用阵列分析，这一无内含子基因在两例原发性结肠癌中的表达显著上调。[由RefSeq提供，2008年7月]This gene is a member
ChIP－using－plant－samples
实验概要 The immunoprecipitation (IP) of cross-linked chromatin with antibodies specific for certain histone modifications (chromatin immunoprecipitati
Deglycosylation－of－Glycoproteins－Using－Endoglycosidases
T.H. Plummer, Jr. and A.L. Tarentino, Department of Biochemistry, New York State Department of Health, Wadsworth Center for Laboratories and Research,
Comprehensive－identification－of－novel－proteins－and－Nglycosylation－sites四
Figure 2 Distribution of N-glycopeptides analyzed by different enriched methods and instruments of royal jelly proteins. A is the distribution of N-