Creating recombination-activated genes and sequence-defined mutant libraries using transposons.

Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Research Abstract Details 

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Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Abstract Text:

Larry Gallagher,Cheri Turner,Elizabeth Ramage,Colin Manoil,

The properties of a collection of transposon Tn5 derivatives that generate reporter gene fusions and internal protein tags are summarized. Procedures utilizing several of the transposons for generating genes activated by Cre-loxP recombination and for creating large sequence-defined mutant libraries are described in detail.

Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Publishing Authors By Initials

L Gallagher,C Turner,E Ramage,C Manoil,

For similar genetic processes: recombination, genetic research abstracts see: genetic processes: recombination, genetic research

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Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Journal Published:

PUBLICATION TYPE: Review

Journal: Methods in enzymology

VOLUME: 421

Page Numbers: 126-40

Journal Abbreviation: Meth. Enzymol.

ISSN: 0076-6879

DAY: 3

MONTH: 12

YEAR: 2007

Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Information

Number of References: 20

LANGUAGE: eng

NlmUniqueID: 212271

Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Keywords Mesh Terms:

KEYWORDS: Recombination, Genetic

MESH TERMS:

Chemical & Substance for Abstract: Creating recombination-activated genes and sequence-defined mutant libraries using transposons. Information

Substance Name: DNA Transposable Elements

Registry Number: 0

Grant and Affiliation Information for Creating recombination-activated genes and sequence-defined mutant libraries using transposons.

AFFILIATION: Department of Genome Sciences, University of Washington, Seattle, WA, USA.

Country: United States

AGENCY: United States NIAID

GRANT: 1U54 AI 57141

ACRONYM: AI

MEDLINETA: Methods Enzymol

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