Vectors for efficient and high-throughput construction of fluorescent Drosophila reporters using the PhiC31 site-specific integration system

Genesis

Volumn 48, Issue 7, 2010, Pages 452-456

  Boy, Aurelia L ^a   Zhai, Zongzhao ^a   Habring Müller, Anette ^b   Kussler Schneider, Yvonne ^a   Kaspar, Petra ^a   Lohmann, Ingrid ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b MAX PLANCK INSTITUTE FOR DEVELOPMENTAL BIOLOGY   (Germany)

Author keywords

Drosophila; eGFP; Gateway system; mCherry; PhiC31 integrase; Reporter lines; Transgenesis; Venus

Indexed keywords

ENHANCED GREEN FLUORESCENT PROTEIN; INTEGRASE; PHIC31; PLASMID VECTOR; UNCLASSIFIED DRUG; HYBRID PROTEIN;

ARTICLE; CLONING; CLONING VECTOR; DROSOPHILA; EMBRYO; ENHANCER REGION; GENE CONSTRUCT; GENE EXPRESSION; GENE INSERTION; GENE LOCUS; GENETIC RECOMBINATION; GENOMICS; HIGH THROUGHPUT SCREENING; INSECT GENOME; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REGULATORY MECHANISM; REPORTER GENE; ANIMAL; BINDING SITE; DROSOPHILA MELANOGASTER; GENE EXPRESSION REGULATION; GENE TRANSFER; GENE VECTOR; GENETICS; METABOLISM; MOLECULAR CLONING; PLASMID; PROCEDURES; PROMOTER REGION; TRANSGENIC ANIMAL;

ANIMALIA;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; BINDING SITES; CLONING, MOLECULAR; DROSOPHILA MELANOGASTER; ENHANCER ELEMENTS, GENETIC; GENE EXPRESSION REGULATION; GENE TRANSFER TECHNIQUES; GENES, REPORTER; GENETIC VECTORS; HIGH-THROUGHPUT SCREENING ASSAYS; INTEGRASES; PLASMIDS; PROMOTER REGIONS, GENETIC; RECOMBINANT FUSION PROTEINS; RECOMBINATION, GENETIC;

EID: 77954713658     PISSN: 1526954X     EISSN: 1526968X     Source Type: Journal    
DOI: 10.1002/dvg.20637     Document Type: Article

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