Evidence map›Paper›PMID 42867791›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2027

Modular Cloning for Rapid Generation of Recombinant Plasmids for Analyses of Salmonella enterica Pathogenesis.

Michael Hensel

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Michael HenselAbteilung Mikrobiologie and CellNanOs-Center of Cellular Nanoanalytics Osnabrück Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany. Michael.Hensel@uni-osnabrueck.de.ORCID http://orcid.org/0000-0001-6604-6253

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analyses of virulence functions of Salmonella enterica demand generation of plasmids for complementation of mutated genes, expression of tagged alleles of effector proteins of the type III secretion systems, or fusions to reporter genes for investigation of regulation of expression, or protein localization and fate after translocation into host cells. Here, a simple and versatile approach for generation of plasmids from modular DNA fragments is described. The Modular Cloning approach is based on Gibson assembly and uses standardized overlap sequences that enable various combinations and reuse of fragments. Modular Cloning does not demand the introduction of sites for restriction enzymes or commercial cloning kits and allows rapid generation of plasmids for various applications in cellular and molecular microbiology of S. enterica.

Indexed as

Cloning, MolecularPlasmidsSalmonella entericaGibson assembly cloningModular cloning techniqueRecombinant plasmidsSynthetic biology

Identifiers

PMID42867791

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.