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yeast genomic library  (ATCC)


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    Structured Review

    ATCC yeast genomic library
    Yeast Genomic Library, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 115 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/yeast+genomic+library/YEp13/pmc13093828-455-7-10
    Average 94 stars, based on 115 article reviews
    yeast genomic library - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Yeast J-protein Sis1 prevents prion toxicity by moderating depletion of prion protein
    Article Snippet: .. We repeated the screen using a separate, randomly assembled yeast genomic library on a TRP1 -based high-copy plasmid obtained from ATCC (cat. no 77162). ..

    Article Title: The proteasome biogenesis regulator Rpn4 cooperates with the unfolded protein response to promote resistance to endoplasmic reticulum stress
    Article Snippet: .. Strain SSY1341 was transformed with a yeast genomic library in the YEp13 multicopy vector ( ; available from the American Type Culture Collection as ATCC 37323; kindly provided by Michael Knop, ZMBH). ..

    Article Title: The proteasome biogenesis regulator Rpn4 cooperates with the unfolded protein response to promote ER stress resistance
    Article Snippet: .. Strain SSY1341 was transformed with a yeast genomic library in the YEp13 multicopy vector ( ; available from the American Type Culture Collection as ATCC 37323; kindly provided by Michael Knop, ZMBH). ..

    Article Title: Cloning of the SPO11 gene that complements a meiotic recombination defect in sake yeast.
    Article Snippet: Please cite Bioeng., htt Cross hybridization breeding of sake yeasts is hampered by difficulty in acquisition of haploid cells through sporulation.. We previously demonstrated that typical sake yeast strains were defective in meiotic chromosome recombination, which caused poor sporulation and loss of spore viability.. In this study, we screened a single copy plasmid genomic DNA library of the laboratory Saccharomyces cerevisiae GRF88 for genes that might complement the meiotic recombination defect of UTCAH-3, a strain derived from the sake yeast Kyokai no. 7 (K7).

    Transformation Assay:

    Article Title: The proteasome biogenesis regulator Rpn4 cooperates with the unfolded protein response to promote resistance to endoplasmic reticulum stress
    Article Snippet: .. Strain SSY1341 was transformed with a yeast genomic library in the YEp13 multicopy vector ( ; available from the American Type Culture Collection as ATCC 37323; kindly provided by Michael Knop, ZMBH). ..

    Article Title: Aegeline, a natural product from the plant Aegle marmelos, mimics the yeast SNARE protein Sec22p in suppressing α-synuclein and Bax toxicity in yeast.
    Article Snippet: Herein, we have identified yeast Sec22p (ySec22p), a SNARE protein essential for endoplasmic reticulum to Golgi trafficking, as a suppressor of Bax-induced yeast apoptosis and corroborated published observations that ySec22p suppresses α-synuclein’s toxicity in yeast.. It has been suggested that compounds which enhance expression, in neurons, of human homologues of ySec22p (Sec22Bp/Sec22p/Sec22A) would prevent synucleinopathies, such as Parkinson’s disease.. With the aim of finding a small molecule that would mimic ySec22p, a library of natural products consisting of 394-compounds was screened using yeast cells that express either human α-synuclein or human Bax.

    Article Title: The proteasome biogenesis regulator Rpn4 cooperates with the unfolded protein response to promote ER stress resistance
    Article Snippet: .. Strain SSY1341 was transformed with a yeast genomic library in the YEp13 multicopy vector ( ; available from the American Type Culture Collection as ATCC 37323; kindly provided by Michael Knop, ZMBH). ..

    Article Title: TOR-dependent regulation of the yeast homolog of the juvenile Batten Disease-associated gene CLN3
    Article Snippet: .. Yeast strain, LWY031, was transformed with a yeast genomic library (ATCC 37323, Yep13 based) and colonies were selected on minimal media without leucine and histidine and in the presence of 3-aminotriazole (1 mM). ..

    Article Title: Cloning of the SPO11 gene that complements a meiotic recombination defect in sake yeast.
    Article Snippet: Please cite Bioeng., htt Cross hybridization breeding of sake yeasts is hampered by difficulty in acquisition of haploid cells through sporulation.. We previously demonstrated that typical sake yeast strains were defective in meiotic chromosome recombination, which caused poor sporulation and loss of spore viability.. In this study, we screened a single copy plasmid genomic DNA library of the laboratory Saccharomyces cerevisiae GRF88 for genes that might complement the meiotic recombination defect of UTCAH-3, a strain derived from the sake yeast Kyokai no. 7 (K7).

    Construct:

    Article Title: Aegeline, a natural product from the plant Aegle marmelos, mimics the yeast SNARE protein Sec22p in suppressing α-synuclein and Bax toxicity in yeast.
    Article Snippet: Herein, we have identified yeast Sec22p (ySec22p), a SNARE protein essential for endoplasmic reticulum to Golgi trafficking, as a suppressor of Bax-induced yeast apoptosis and corroborated published observations that ySec22p suppresses α-synuclein’s toxicity in yeast.. It has been suggested that compounds which enhance expression, in neurons, of human homologues of ySec22p (Sec22Bp/Sec22p/Sec22A) would prevent synucleinopathies, such as Parkinson’s disease.. With the aim of finding a small molecule that would mimic ySec22p, a library of natural products consisting of 394-compounds was screened using yeast cells that express either human α-synuclein or human Bax.

    Cloning:

    Article Title: Cloning of the SPO11 gene that complements a meiotic recombination defect in sake yeast.
    Article Snippet: Please cite Bioeng., htt Cross hybridization breeding of sake yeasts is hampered by difficulty in acquisition of haploid cells through sporulation.. We previously demonstrated that typical sake yeast strains were defective in meiotic chromosome recombination, which caused poor sporulation and loss of spore viability.. In this study, we screened a single copy plasmid genomic DNA library of the laboratory Saccharomyces cerevisiae GRF88 for genes that might complement the meiotic recombination defect of UTCAH-3, a strain derived from the sake yeast Kyokai no. 7 (K7).

    Marker:

    Article Title: Cloning of the SPO11 gene that complements a meiotic recombination defect in sake yeast.
    Article Snippet: Please cite Bioeng., htt Cross hybridization breeding of sake yeasts is hampered by difficulty in acquisition of haploid cells through sporulation.. We previously demonstrated that typical sake yeast strains were defective in meiotic chromosome recombination, which caused poor sporulation and loss of spore viability.. In this study, we screened a single copy plasmid genomic DNA library of the laboratory Saccharomyces cerevisiae GRF88 for genes that might complement the meiotic recombination defect of UTCAH-3, a strain derived from the sake yeast Kyokai no. 7 (K7).



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    ATCC high copy yeast genomic dna library
    Screening of a genomic library for arsenic resistance in yeast and identified hits. (a) Cartoon of the screening setup and arsenic concentrations used. Growth of yeast <t>gDNA</t> transformants on gradient plates containing (b) arsenate [As(V)] and (c) arsenite [As(III)]. Growth was scored after incubating the cells for 3–5 days at 30°C. P‐only represents the empty vector containing cells.
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    Screening of a genomic library for arsenic resistance in yeast and identified hits. (a) Cartoon of the screening setup and arsenic concentrations used. Growth of yeast <t>gDNA</t> transformants on gradient plates containing (b) arsenate [As(V)] and (c) arsenite [As(III)]. Growth was scored after incubating the cells for 3–5 days at 30°C. P‐only represents the empty vector containing cells.
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    Image Search Results


    Screening of a genomic library for arsenic resistance in yeast and identified hits. (a) Cartoon of the screening setup and arsenic concentrations used. Growth of yeast gDNA transformants on gradient plates containing (b) arsenate [As(V)] and (c) arsenite [As(III)]. Growth was scored after incubating the cells for 3–5 days at 30°C. P‐only represents the empty vector containing cells.

    Journal: MicrobiologyOpen

    Article Title: Identification of novel arsenic resistance genes in yeast

    doi: 10.1002/mbo3.1284

    Figure Lengend Snippet: Screening of a genomic library for arsenic resistance in yeast and identified hits. (a) Cartoon of the screening setup and arsenic concentrations used. Growth of yeast gDNA transformants on gradient plates containing (b) arsenate [As(V)] and (c) arsenite [As(III)]. Growth was scored after incubating the cells for 3–5 days at 30°C. P‐only represents the empty vector containing cells.

    Article Snippet: High copy yeast genomic DNA library (AB320 genomic DNA library in YEp13 plasmid in Escherichia coli obtained from the American Type Culture Collection ATCC [No: 37323]) was introduced into yeast cells by transformation for subsequent genomic library screening.

    Techniques: Plasmid Preparation

    Growth of yeast gDNA transformants on plates containing given concentrations of (a) arsenate [As(V)] and (b) arsenite [As(III)]. Growth was scored after incubating the cells for 5 days at 30°C. P‐only represents the empty vector.

    Journal: MicrobiologyOpen

    Article Title: Identification of novel arsenic resistance genes in yeast

    doi: 10.1002/mbo3.1284

    Figure Lengend Snippet: Growth of yeast gDNA transformants on plates containing given concentrations of (a) arsenate [As(V)] and (b) arsenite [As(III)]. Growth was scored after incubating the cells for 5 days at 30°C. P‐only represents the empty vector.

    Article Snippet: High copy yeast genomic DNA library (AB320 genomic DNA library in YEp13 plasmid in Escherichia coli obtained from the American Type Culture Collection ATCC [No: 37323]) was introduced into yeast cells by transformation for subsequent genomic library screening.

    Techniques: Plasmid Preparation