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cytomat ambient hotel  (Thermo Fisher)


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    Thermo Fisher cytomat ambient hotel
    Cytomat Ambient Hotel, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytomat+hotel/cytomat+ambient+hotel/pmc11949028__jciinsight___10___181496___s127-12-33-37
    Average 90 stars, based on 1 article reviews
    cytomat ambient hotel - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Development and Validation of an Automated High-Throughput System for Zebrafish In Vivo Screenings
    Article Snippet: The HTS platform integrates an embryo sorter adapted from the Copas XL from Union Biometrica with a larger embryo reservoir and specific sensors and alarms, two liquid handling devices (Starlet’s from Hamilton), a plate-feeder carrousel (Cytomat Hotel from Thermo), an automatic incubator (Cytomat from Thermo), a reader (fully motorized inverted microscope Axiovert 200 M from Zeiss and EMCCD camera from Hamamatsu) and a robotic arm (TX60 from Staubli) as shown in .

    Sequencing:

    Article Title: Total synthesis of long DNA sequences: Synthesis of a contiguous 32-kb polyketide synthase gene cluster
    Article Snippet: .. Gene synthesis and sequencing were assisted by an integrated automation system consisting of a BioMek FX, a robotic ORCA arm, and a tip lift (Beckman Coulter), plate sealer and piercer (Velocity11), Palo Alto, CA), two tetrad thermal cyclers (MJ Research, Cambridge, MA), and a cytomat hotel (Kendro, Asheville, NC). .. Vector Construction.

    Fluorescence:

    Article Title: Coupled high-throughput functional screening and next generation sequencing for identification of plant polymer decomposing enzymes in metagenomic libraries.
    Article Snippet: .. Absorbance and fluorescence readings were recorded after 24 h and 5 days using an automated workflow on an integrated Biomek FXp Workstation (Beckman Coulter) with Cytomat hotel (Thermo Scientific, Waltham, MA, USA), 6K15 centrifuge (Sigma Laborzentrifugen GmbH, Osterode, Germany), fly-by bar code reader (Beckman Coulter), and Paradigm multimode scanner (Molecular Devices). ..

    Incubation:

    Article Title: Designs and Concept-Reliance of a Fully Automated High Content Screening Platform
    Article Snippet: .. A high capacity incubator Cytomat 24C (Thermo Fisher Scientific), set at 37°C, 5% CO 2 and 98% humidity and a Cytomat Hotel (Thermo Fisher Scientific) ambient temperature incubator, are used for sample plate incubation and storage, varying on the onboard assay conditions. .. The fixing and staining process performed on deck is done by using three MultiDrop Combis (Thermo Fisher Scientific) with three ELx405 Washers (BioTek Instruments, Winooski, WI) and an ABgene3000 (Thermo Fisher Scientific), sealing the sample plates.



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    Optical density of A) P . chrysogenum KF657, B) D . salina LF304, C) H . varia KF560, D) A . cruciatus LF680, E) Tritiracium sp. LF562, F) P . pinophilum LF458, G) M . brevicaulis LF580 and H) Calcarisporium sp. KF525. Mycelia were grown in defined medium buffered at pH 4.25 with glucose (red), xylose (blue), galactose (cyan) or glycerol (green) as carbon source, or no added carbon source (grey) in 300 μl cultures in 100-well plates in a BioScreen C (1) or 150 μl cultures in 96-well plates in a <t>Cytomat</t> <t>plate</t> hotel (2). Error bars represent ± standard error of the mean (sem) for 3 to 6 replicates. Note that a short break in the power supply disturbed data collection after 110 hours for M . breviaculis LF580 and Calcarisporium sp. KF525. Data collection was restored after 160 hours.
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    Optical density of A) P . chrysogenum KF657, B) D . salina LF304, C) H . varia KF560, D) A . cruciatus LF680, E) Tritiracium sp. LF562, F) P . pinophilum LF458, G) M . brevicaulis LF580 and H) Calcarisporium sp. KF525. Mycelia were grown in defined medium buffered at pH 4.25 with glucose (red), xylose (blue), galactose (cyan) or glycerol (green) as carbon source, or no added carbon source (grey) in 300 μl cultures in 100-well plates in a BioScreen C (1) or 150 μl cultures in 96-well plates in a <t>Cytomat</t> <t>plate</t> hotel (2). Error bars represent ± standard error of the mean (sem) for 3 to 6 replicates. Note that a short break in the power supply disturbed data collection after 110 hours for M . breviaculis LF580 and Calcarisporium sp. KF525. Data collection was restored after 160 hours.
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    Image Search Results


    Optical density of A) P . chrysogenum KF657, B) D . salina LF304, C) H . varia KF560, D) A . cruciatus LF680, E) Tritiracium sp. LF562, F) P . pinophilum LF458, G) M . brevicaulis LF580 and H) Calcarisporium sp. KF525. Mycelia were grown in defined medium buffered at pH 4.25 with glucose (red), xylose (blue), galactose (cyan) or glycerol (green) as carbon source, or no added carbon source (grey) in 300 μl cultures in 100-well plates in a BioScreen C (1) or 150 μl cultures in 96-well plates in a Cytomat plate hotel (2). Error bars represent ± standard error of the mean (sem) for 3 to 6 replicates. Note that a short break in the power supply disturbed data collection after 110 hours for M . breviaculis LF580 and Calcarisporium sp. KF525. Data collection was restored after 160 hours.

    Journal: PLoS ONE

    Article Title: High throughput, small scale methods to characterise the growth of marine fungi

    doi: 10.1371/journal.pone.0236822

    Figure Lengend Snippet: Optical density of A) P . chrysogenum KF657, B) D . salina LF304, C) H . varia KF560, D) A . cruciatus LF680, E) Tritiracium sp. LF562, F) P . pinophilum LF458, G) M . brevicaulis LF580 and H) Calcarisporium sp. KF525. Mycelia were grown in defined medium buffered at pH 4.25 with glucose (red), xylose (blue), galactose (cyan) or glycerol (green) as carbon source, or no added carbon source (grey) in 300 μl cultures in 100-well plates in a BioScreen C (1) or 150 μl cultures in 96-well plates in a Cytomat plate hotel (2). Error bars represent ± standard error of the mean (sem) for 3 to 6 replicates. Note that a short break in the power supply disturbed data collection after 110 hours for M . breviaculis LF580 and Calcarisporium sp. KF525. Data collection was restored after 160 hours.

    Article Snippet: For growth in 96-well plates, NuncTM Flat Bottom 96-well Clear Polystyrene Plates (Thermo Scientific 260860; well depth 11.4 mm, well diameter 7 mm at top) containing 145 μl medium were inoculated with 7.5 μl conidial or mycelial suspension and incubated at 24°C with 1100 rpm agitation in a Thermo Scientific Cytomat plate hotel (throw = 1 mm; holding up to 23 plates).

    Techniques: