Visualizing Endogenous mRNAs in Living Yeast Using m-TAG, a PCR-Based RNA Aptamer Integration Method, and Fluorescence Microscopy

Methods in Molecular Biology

Volumn 714, Issue , 2011, Pages 237-247

  Haim Vilmovsky, Liora ^b   Gerst, Jeffrey E ^a  

^a WEIZMANN INSTITUTE OF SCIENCE   (Israel)

^b NONE

Author keywords

Cre recombinase; Gene tagging; Green fluorescent protein; mRNA; MS2; Saccharomyces cerevisiae; Yeast

Indexed keywords

APTAMER; CRE RECOMBINASE; DNA; FUNGAL RNA; INTEGRASE; MESSENGER RNA;

ARTICLE; CYTOLOGY; FLUORESCENCE MICROSCOPY; GENETIC TRANSFORMATION; GENETICS; IMMOBILIZED CELL; ISOLATION AND PURIFICATION; METABOLISM; METHODOLOGY; MOLECULAR IMAGING; MOLECULAR PROBE; POLYMERASE CHAIN REACTION; PRECIPITATION; SACCHAROMYCES CEREVISIAE;

APTAMERS, NUCLEOTIDE; CELLS, IMMOBILIZED; CHEMICAL PRECIPITATION; DNA; INTEGRASES; MICROSCOPY, FLUORESCENCE; MOLECULAR IMAGING; MOLECULAR PROBES; POLYMERASE CHAIN REACTION; RNA, FUNGAL; RNA, MESSENGER; SACCHAROMYCES CEREVISIAE; TRANSFORMATION, GENETIC;

EID: 79960038127     PISSN: 10643745     EISSN: 19406029     Source Type: Book Series    
DOI: 10.1007/978-1-61779-005-8_15     Document Type: Chapter

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