A one pot, one step, precision cloning method with high throughput capability - Test2 - elhamkhani - TriplyDB

A one pot, one step, precision cloning method with high throughput capability

A one pot, one step, precision cloning method with high throughput capability

http://www.wikidata.org/entity/Q33382728

about

Transcriptional activators of human genes with programmable DNA-specificity Small RNA sX13: a multifaceted regulator of virulence in the plant pathogen Xanthomonas Assembly of designer TAL effectors by Golden Gate cloning Genome-scale engineering for systems and synthetic biology Efficient construction of sequence-specific TAL effectors for modulating mammalian transcription Testing the causality between CYP9M10 and pyrethroid resistance using the TALEN and CRISPR/Cas9 technologies Techniques for the Analysis of Protein-Protein Interactions in Vivo From Gene Targeting to Genome Editing: Transgenic animals applications and beyond Synthetic analog and digital circuits for cellular computation and memory Optogenetic control of nuclear protein export.Genetically engineering self-organization of human pluripotent stem cells into a liver bud-like tissue using Gata6.An asymmetric SMC-kleisin bridge in prokaryotic condensin High-throughput recombinant protein expression in Escherichia coli: current status and future perspectives Synthetic biology to access and expand nature's chemical diversity Detection and functional characterization of a 215 amino acid N-terminal extension in the Xanthomonas type III effector XopD A rapid cloning method employing orthogonal end protection Intraradical colonization by arbuscular mycorrhizal fungi triggers induction of a lipochitooligosaccharide receptor End-to-end automated microfluidic platform for synthetic biology: from design to functional analysis Developments in the tools and methodologies of synthetic biology A survey of enabling technologies in synthetic biology High-throughput protein expression using a combination of ligation-independent cloning (LIC) and infrared fluorescent protein (IFP) detection A modular cloning system for standardized assembly of multigene constructs GoldenBraid: an iterative cloning system for standardized assembly of reusable genetic modules Quick and clean cloning: a ligation-independent cloning strategy for selective cloning of specific PCR products from non-specific mixes Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting Dissecting virulence function from recognition: cell death suppression in Nicotiana benthamiana by XopQ/HopQ1-family effectors relies on EDS1-dependent immunity.The Predicted Lytic Transglycosylase HpaH from Xanthomonas campestris pv. vesicatoria Associates with the Type III Secretion System and Promotes Effector Protein Translocation.A TAL-Based Reporter Assay for Monitoring Type III-Dependent Protein Translocation in Xanthomonas.Arabidopsis thaliana DM2h (R8) within the Landsberg RPP1-like Resistance Locus Underlies Three Different Cases of EDS1-Conditioned Autoimmunity.Type III-Dependent Translocation of HrpB2 by a Nonpathogenic hpaABC Mutant of the Plant-Pathogenic Bacterium Xanthomonas campestris pv. vesicatoria Arabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate geranylfarnesyl diphosphate.Standards for plant synthetic biology: a common syntax for exchange of DNA parts.Xanthomonas campestris pv. vesicatoria Secretes Proteases and Xylanases via the Xps Type II Secretion System and Outer Membrane Vesicles.A library of synthetic transcription activator-like effector-activated promoters for coordinated orthogonal gene expression in plants Refined requirements for protein regions important for activity of the TALE AvrBs3.High-level diterpene production by transient expression in Nicotiana benthamiana The periplasmic HrpB1 protein from Xanthomonas spp. binds to peptidoglycan and to components of the type III secretion system.HrcQ provides a docking site for early and late type III secretion substrates from Xanthomonas Analysis of new type III effectors from Xanthomonas uncovers XopB and XopS as suppressors of plant immunity.Functional characterization of the type III secretion substrate specificity switch protein HpaC from Xanthomonas campestris pv. vesicatoria.

P2860

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P2860

A one pot, one step, precision cloning method with high throughput capability

http://www.wikidata.org/entity/Q33382728

description

2008 nî lūn-bûn

@nan

2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

A one pot, one step, precision cloning method with high throughput capability

@ast

A one pot, one step, precision cloning method with high throughput capability

@en

type

label

A one pot, one step, precision cloning method with high throughput capability

@ast

A one pot, one step, precision cloning method with high throughput capability

@en

prefLabel

A one pot, one step, precision cloning method with high throughput capability

@ast

A one pot, one step, precision cloning method with high throughput capability

@en

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JOURNAL.PONE.0003647

P1433

P1476

A one pot, one step, precision cloning method with high throughput capability

@en

P2093

Carola Engler

http://www.w3.org/2001/XMLSchema#string

Romy Kandzia

http://www.w3.org/2001/XMLSchema#string

Sylvestre Marillonnet

http://www.w3.org/2001/XMLSchema#string

P2860

Many paths to many clones: a comparative look at high-throughput cloning methods

In planta engineering of viral RNA replicons: efficient assembly by recombination of DNA modules delivered by Agrobacterium.

Rapid high-yield expression of full-size IgG antibodies in plants coinfected with noncompeting viral vectors.

Modification of the Creator recombination system for proteomics applications--improved expression by addition of splice sites.

Seamless cloning and gene fusion.

NOMAD: a versatile strategy for in vitro DNA manipulation applied to promoter analysis and vector design.

Class-IIS restriction enzymes--a review.

Introduction of arbitrary sequences into genes by use of class IIs restriction enzymes.

Method of artificial DNA splicing by directed ligation (SDL).

Rapid single step subcloning procedure by combined action of type II and type IIs endonucleases with ligase.

P304

e3647

http://www.w3.org/2001/XMLSchema#string

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scholarly article

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10.1371/JOURNAL.PONE.0003647

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P407

P433

11

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P478

3

http://www.w3.org/2001/XMLSchema#string

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2008-11-05T00:00:00Z

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23452410

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18985154

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2574415

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