AMethodforAssayingDeubiquitinatingEnzymes2
Table 1: Hydrolysis of 125I-labeled Ub-PESTc by the purified YUH1.Specific activity againstDUBsCbz-LRGG-AMC125I-labeled Ub-PESTcYUH13.2 x 10-105.1 x 10-8yUBP62.0 x 10-123.2 x 10-9cUCH-10.7 x 10-112.8 x 10-7cUCH-61.2 x 10-101.1 x 10-6cUCH-80.9 x 10-113.3 x 10-7cUBP412.5 x 10-115.3 x 10-7125I-labeled Ub-PESTc (20 μg) was incubated with YUH1 (0.1 μg) at 37 °C for various periods in the presence and absence of 1 μg ......阅读全文
A－Method－for－Assaying－Deubiquitinating－Enzymes2
Table 1: Hydrolysis of 125I-labeled Ub-PESTc by the purified YUH1.Specific activity againstDUBsCbz-LRGG-AMC125I-labeled Ub-PESTcYUH13.2 x 10-105.1 x 1
A－Method－for－Assaying－Deubiquitinating－Enzymes1
AbstractA general method for the assay of deubiquitinating enzymes was described in detail using 125I-labeled ubiquitin-fused αNH-MHISPPEPESEEEEEHYC (
yeast:Assaying－mating
SetupYou have yeast strains that are deficient in mating (eg Ste12 knockouts) and would like to test whether transforming them with a plasmid that con
creativeenzymes工业用酶
化学加工作为具有高反应速率的可持续催化剂，酶已引起了化学催化剂以外的更多关注。如今，由于清洁和高效的催化性能，越来越多的化学过程被酶所取代。例如，在手性合成中，酶显示出极高的立体特异性，这是化学催化剂所没有的，这简化了整个合成过程。环境与废物管理酶是天然催化剂，可选择性分解较大分子的混合物。在酶技术
Method:－Lymphocyte－Transformation
Method: Lymphocyte TransformationMay 30, 1990Rosalie VeilePrinciple:Lymphocytes are transformed to establish cell lines. Mononuclear cells (lymphocyte
Easy－YAC－Preparation－Method
YAC TRANSFORMATION OF C. ELEGANS USING TOTAL YEAST GENOMIC DNA[This method is described in The Worm Breeder's Gazette (1997) A. Davies and J. Shaw
A－Method－for－Structure5
ConclusionsQuorum-sensing signaling systems involving the interaction between a signaling peptide and its cognate histidine kinase receptor are widely
A－Method－for－Structure3
CSP-Dependent Transformation AssayTo determine if synthetic peptides activated quorum sensing for induction of genetic competence, we used the comC de
A－Method－for－Structure2
CD SpectroscopyCD spectra for peptides and reference solutions were recorded at 298 K on a Jasco J-920 CD spectrometer with a 1-mm quartz cuvette. Spe
A－Method－for－Structure1
A Method for Structure–Activity Analysis of Quorum-Sensing Signaling Peptides from Naturally Transformable StreptococciMany species of streptococci se
A－Method－for－Structure4
We also used this mutant (SMdC) as a host to generate two types of lacZ transcriptional reporter fusion strains to assay the promoter activity of QS-c
A－quick－method－to－isolate－plant
Use from 0.01 - 0.1 gram plant material. Grind the plant material with liq.N2 in a mortar.We normally use some alumina to crush hard tissue.
内切酶列表：Enzymes－Generating－Blunt－Ends
Asymmetric sequences are indicated by *.Single letter code:R = G or A; Y = C or T; W = A or T; M = A or C; K = G or T; S = C or G;H = A, C or T;V = A,
内切酶列表：Enzymes－Generating－Blunt－Ends
Asymmetric sequences are indicated by *.Single letter code:R = G or A; Y = C or T; W = A or T; M = A or C; K = G or T; S = C or G;H = A, C or T;V = A,
内切酶列表：Enzymes－Generating－5protruding－Ends
Asymmetric sequences are indicated by *.Single letter code:R = G or A; Y = C or T; W = A or T; M = A or C; K = G or T; S = C or G;H = A, C or T;V = A,
内切酶列表：Enzymes－Generating－3protruding－Ends
Asymmetric sequences are indicated by *.Single letter code:R = G or A; Y = C or T; W = A or T; M = A or C; K = G or T; S = C or G;H = A, C or T;V = A,
Basic－Method－for－Indirect－Immunofluorescence－Labeling
Basic Method for Indirect Immunofluorescence LabelingBackgroundThis is the method for indirect immunofluorescence labeling; that is, the antibodies do
Method:－Maintaining－Lymphoblastoid－Cell－Lines
Method: Maintaining Lymphoblastoid Cell LinesJune 10, 1990Rosalie VeilePurpose:To grow lymphoblastoid cells for permanent storage and for DNA extracti
MN－in－Human－Lymphocytes－(method－description)
MN in Human Lymphocytes (method description)Lymphocyte isolation Lymphocytes were isolated using Ficoll-Paque density gradients. Blood was diluted
Method:－Logging－in－Specimens－and－Record－Keeping
Method: Logging in Specimens and Record KeepingJune 10, 1990Rosalie VeilePurpose:To keep a written and computerized record of all cell lines, the date
Method:－Cell－Counts－Using－a－Hemacytometer
Method: Cell Counts Using a HemacytometerJune 1, 1990Rosalie VeilePurpose:The purpose of this procedure is to determine the cell density of the cultur
Methylation－of－Fatty－Acids－(Kropinski－Method)
Methylation of Fatty Acids (Kropinski Method)OBJECTIVE:To methylate fatty acids in whole cells or lipopolysaccharide.REAGENTS :Methanol-Hydrochloride
Assay－of－superoxide－dismutase－activity1
Assay of superoxide dismutase activity by combining electrophoresis and densitometryAbstract. A modified technique was developed to assay superoxide d
A－novel－method－of－growing－fungi－for－DNA－extraction
Preparation of fungi for DNA extraction typically involves growing cultures in liquid culture in Erlenmeyer flasks, Roux bottles or even microfuge tub
Large－Scale－Plasmid－Preps:－PEG－method
1. Grow 250 500 mL of bacteria overnight in LB with 50 µg/mL of ampicillin.2. Transfer culture to Nalgene bottles. Spin in SGA rotor at 6000 rpm, at
Ethanol－precipitation－method－for－purifying－PCR－products
1. For each PCR reaction (50 µL) prepare a 1.5mL microcentrifuge tube containing the following: - 5 µL of 3M sodium acetate (NaOAc), pH 4.6
A－rapid,－quantitative－and－inexpensive－method－for－detecting－apoptosis
ASTRACTWe describe a rapid and quantitative flow cytometric method for determining the apoptotic or anti-apoptotic potential of a gene in various cell
Ethanol－precipitation－method－for－purifying－PCR－products
1. For each PCR reaction (50 µL) prepare a 1.5mL microcentrifuge tube containing the following: - 5 µL of 3M sodium acetate (NaOAc), pH 4.6
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
Method:－Preparation－of－Lymphocyte－Cell－Pellet－for－Storage
Method: Preparation of Lymphocyte Cell Pellet for StorageJune 10, 1990Rosalie VeilePurpose:Following propagation to 1 X 108 cells, lymphoblastoid cell