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Cloning

About: Cloning is a research topic. Over the lifetime, 6465 publications have been published within this topic receiving 164540 citations. The topic is also known as: clone & organism cloning.


Papers
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Book ChapterDOI

4,611 citations

Journal ArticleDOI
TL;DR: A deletion of three base pairs that results in the omission of a phenylalanine residue at the center of the first predicted nucleotide-binding domain was detected in CF patients.

2,946 citations

Journal ArticleDOI
TL;DR: A Gateway-compatible Agrobacterium sp.
Abstract: The current challenge, now that two plant genomes have been sequenced, is to assign a function to the increasing number of predicted genes. In Arabidopsis, approximately 55% of genes can be assigned a putative function, however, less than 8% of these have been assigned a function by direct experimental evidence. To identify these functions, many genes will have to undergo comprehensive analyses, which will include the production of chimeric transgenes for constitutive or inducible ectopic expression, for antisense or dominant negative expression, for subcellular localization studies, for promoter analysis, and for gene complementation studies. The production of such transgenes is often hampered by laborious conventional cloning technology that relies on restriction digestion and ligation. With the aim of providing tools for high throughput gene analysis, we have produced a Gateway-compatible Agrobacterium sp. binary vector system that facilitates fast and reliable DNA cloning. This collection of vectors is freely available, for noncommercial purposes, and can be used for the ectopic expression of genes either constitutively or inducibly. The vectors can be used for the expression of protein fusions to the Aequorea victoria green fluorescent protein and to the β-glucuronidase protein so that the subcellular localization of a protein can be identified. They can also be used to generate promoter-reporter constructs and to facilitate efficient cloning of genomic DNA fragments for complementation experiments. All vectors were derived from pCambia T-DNA cloning vectors, with the exception of a chemically inducible vector, for Agrobacterium sp.-mediated transformation of a wide range of plant species.

2,490 citations

Book
01 Jan 1985
TL;DR: The construction and characterization of vaccinia virus recombinants expressing foreign genes Bovine papilloma virus DNA: A eukaryotic cloning vector is studied.
Abstract: Bacillus cloning methods Gene cloning in streptomyces Cloning in yeast Genetic Engineering of plants P element mediated germ line transformation of drosophila High efficiency gene transfer into mammalian cells The construction and characterization of vaccinia virus recombinants expressing foreign genes Bovine papilloma virus DNA: A eukaryotic cloning vector

2,266 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20223
202148
202066
201995
2018128
2017141