Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 6, 1997, Pages 2122-2127

  Haseloff, Jim ^a   Siemering, Kirby R ^a   Prasher, Douglas C ^b   Hodge, Sarah ^a  

^a MRC LABORATORY OF MOLECULAR BIOLOGY   (United Kingdom)

^b UNITED STATES DEPARTMENT OF AGRICULTURE   (United States)

Author keywords

confocal microscopy; cryptic splicing; endoplasmic reticulum; genetic marker; plant transformation

Indexed keywords

HYBRID PROTEIN; NUCLEIC ACID;

ARABIDOPSIS; ARTICLE; CELLULAR DISTRIBUTION; DNA SEQUENCE; ENDOPLASMIC RETICULUM; GENE EXPRESSION; GENE MUTATION; GENETIC CODE; GENETIC TRANSFORMATION; INTRON; JELLYFISH; MARKER GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN ANALYSIS;

ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; ARABIDOPSIS; BASE SEQUENCE; CODON; ENDOPLASMIC RETICULUM; GENETIC MARKERS; GREEN FLUORESCENT PROTEINS; INTRONS; LUMINESCENT PROTEINS; MOLECULAR SEQUENCE DATA; PLANTS, GENETICALLY MODIFIED; PLASMIDS; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING; RHIZOBIUM RADIOBACTER; RNA, MESSENGER; SCYPHOZOA; SEQUENCE DELETION; TRANSCRIPTION, GENETIC; TRANSFORMATION, GENETIC;

AEQUOREA VICTORIA; ARABIDOPSIS; ARABIDOPSIS THALIANA; VICTORIA;

EID: 0030989517     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.6.2122     Document Type: Article

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