Development of the FUN-1 family of fluorescent probes for vacuole labeling and viability testing of yeasts /

QR kód

Development of the FUN-1 family of fluorescent probes for vacuole labeling and viability testing of yeasts /

Uloženo v:

Podrobná bibliografie
Další autoři:	Haugland, R. P., Millard, P. J., Roth, B. L., Thi, H. P., Yue, S. T.
Médium:	Článek
Jazyk:	English
Témata:	Fluorescent labelling Fluorescent tracer Fungi Metabolism Saccharomyces cerevisiae Viability Yeast
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo otaguje tento záznam!

Thư viện lưu trữ:	Thư viện Trường Đại học Đà Lạt

Podobné jednotky

Measurement of the effects of acetic acid and extracellular pH on intracellular pH of nonfermenting, individual saccharomyces cerevisiae cells by fluorescence microscopy /
Autor: Guldfeldt, Lars Uhre.

A flow cytometric method for rapid selection of novel industrial yeast hybrids /

Hydrostatic pressure enhances vital staining with carboxyfluorescein or carboxydichlorofluorescein in saccharomyces cerevisiae : Efficient detection of labeled yeasts by flow cytometry /
Autor: Abe, Fumiyoshi.

Evidence for the interplay between trehalose metabolism and Hsp104 in yeast /

In situ accessibility of saccharomyces cerevisiae 26S rRNA to Cy3-labeled oligonucleotide probes comprising the D1 and D2 domains /

Effectiveness of SYTOX green stain for bacterial viability assessment /
Autor: Lebaron, P.

An inverse correlation between stress resistance and stuck fermentations in wine yeasts. A molecular study /
Autor: Ivorra, Carmen.

Specific cell wall proteins confer resistance to nisin upon yeast cells /

Effect of specific growth rate on fermentative capacity of baker's yeast /
Autor: Hoek, Pim Van

Detection of G proteins by affinity probe capillary electrophoresis using a fluorescently labeled GTP analogue /

Reversible ratiometric probe for quantitative DNA measurements /
Autor: Ueberfeld, Jorn.

Flow cytometric analysis of the in situ accessibility of escherichia coli 16s rrna for fluorescently labeled oligonucleotide probes /

Reproducibility of quantitative proteomic analyses of complex biological mixtures by multidimensional protein identification technology /
Autor: Washburn, Michael P.

Metabolic responses of pyruvate decarboxylase-negative Saccharomyces cerevisiae to glucose excess /
Autor: Flikweert, M. T.

Silencing MIG1 in Saccharomyces cerevisiae : Effects of antisense MIG1 expression and MIG1 gene disruption /

Identification and characterization of phenylpyruvate decarboxylase genes in saccharomyces cerevisiae /

Yeast genome-wide expression analysis identifies a strong ergosterol and oxidative stress response during the initial stages of an industrial lager fermentation /

Effects of inactivation and constitutive expression of the unfolded- protein response pathway on protein production in the yeast saccharomyces cerevisiae /
Autor: Valkonen, Mari.

Direct detection of viable bacteria, molds, yeasts by reverse transcriptase PCR in contaminated milk samples after heat treatment /
Autor: Vaitilingom, Marc.

Assimilation of cellooligosaccharides by a cell surface-engineered yeast expressing -glucosidase and carboxymethylcellulase from aspergillus aculeatus /

A fluorescent gram stain for flow cytometry and epifluorescence microscopy /

Characterization of the cricket hindgut microbiota with fluorescently labeled rRNA-targeted oligonucleotide probes /

Microchemical element imaging of yeast and human cells using synchrotron X-ray microprobe with kirkpatrick-baez optics /

Engineering redox cofactor regeneration for improved pentose fermentation in saccharomyces cerevisiae /

Gene dosage effect of L-proline biosynthetic enzymes on L-proline accumulation and freeze tolerance in saccharomyces cerevisiae /
Autor: Terao, Yukiyasu.

Quantification of toxic cyanobacteria in water by use of competitive PCR followed by sequence-specific labeling of oligonucleotide probes /

Enhanced emission of highly labeled DNA oligomers near silver metallic surfaces /
Autor: Malicka, Joanna.

Thiram and dimethyldithiocarbamic acid interconversion in Saccharomyces cerevisiae : A possible metabolic pathway under the control of the glutathione redox cycle /
Autor: Elskens, M. T.

A new sensitive, whole-cell hybridization technique for detection of bacteria involving a biotinylated oligonucleotide probe targeting rRNA and tyramide signal amplification /

Nitrogen availability of grape juice limits killer yeast growth and fermentation activity during mixed-culture fermentation with sensitive commercial yeast strains /

Metabolic engineering of ammonium assimilation in xylose-fermenting saccharomyces cerevisiae improves ethanol production /
Autor: Roca, Christophe.

Functional expression of a fungal laccase in saccharomyces cerevisiae by directed evolution /

Improvement of nitrogen assimilation and fermentation kinetics under enological conditions by derepression of alternative nitrogen-assimilatory pathways in an industrial saccharomyces cerevisiae strain /
Autor: Salmon, Jean-Michel.

The H+-ATPase in the plasma membrane of saccharomyces cerevisiae is activated during growth latency in octanoic acid-supplemented medium accompanying the decrease in intracellular pH and cell viability /

Evaluation of the redox dye 5-cyano-2,3-tolyl-tetrazolium chloride for activity studies by simultaneous use of microautoradiography and fluorescence in situ hybridization /
Autor: Nielsen, Jeppe Lund.

Disruption of the CAR1 gene encoding arginase enhances freeze tolerance of the commercial baker's yeast saccharomyces cerevisiae /

Effects of overproduction of the catalytic domain of 3-hydroxy-3- methylglutaryl coenzyme A reductase on squalene synthesis in Saccharomyces cerevisiae /
Autor: Donald, K. A.

Genetically controlled cell lysis in the yeast Saccharomyces cerevisiae /

Lysine-overproducing mutants of Saccharomyces cerevisiae baker's yeast isolated in continuous culture /
Autor: Gasent-Ramirez, J. M.

Induction of lipid peroxidation during heavy metal stress in Saccharomyces cerevisiae and influence of plasma membrane fatty acid unsaturation /
Autor: Howlett, N. G.