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nephelostar  (BMG Labtech)


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    BMG Labtech nephelostar
    Nephelostar, supplied by BMG Labtech, used in various techniques. Bioz Stars score: 95/100, based on 223 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nephelostar/NEPHELOstar+Plus/10__1016_slash_j__bbrep__2026__102572-90-10-11
    Average 95 stars, based on 223 article reviews
    nephelostar - by Bioz Stars, 2026-10
    95/100 stars

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    other:

    Article Title: Tuberculous Meningitis with the Soap Bubble Appearance Abscess Formation Resulting from a Paradoxical Reaction during Treatment in an Immunocompetent Host.
    Article Snippet: While treatment options for human African trypanosomiasis (HAT) have improved significantly, there is still a need for new drugs with eradication now a realistic possibility.. Here, we report the development of 2,4-diaminothiazoles that demonstrate significant potency against Trypanosoma brucei, the causative agent of HAT.. Using phenotypic screening to guide structure−activity relationships, potent drug-like inhibitors were developed.

    Article Title: Genetic modules for α‐factor pheromone controlled growth regulation of Saccharomyces cerevisiae
    Article Snippet: Growth of the yeast cells was monitored using the NepheloStar (BMG LABTECH) under following conditions: temperature: 30°C, shaking: 170 rpm, width 3 mm, orbital; cycles: 200, 30 min each.

    Article Title: Hydrogen-Deuterium Exchange Mass Spectrometry Reveals Mechanistic Insights into RNA Oligonucleotide-Mediated Inhibition of TDP-43 Aggregation.
    Article Snippet: Light scattering of 50 μL of each solution in a 96-well plate (Corning Product No. 3881) was then monitored using a Nephelostar (BMG Labtech GmbH) using an excitation wavelength of 635 ± 10 nm, over 6 h at 25 °C.

    Article Title: Hydrogen–Deuterium Exchange Mass Spectrometry Reveals Mechanistic Insights into RNA Oligonucleotide-Mediated Inhibition of TDP-43 Aggregation
    Article Snippet: Light scattering of 50 μL of each solution in a 96-well plate (Corning Product No. 3881) was then monitored using a Nephelostar (BMG Labtech GmbH) using an excitation wavelength of 635 ± 10 nm, over 6 h at 25 °C.

    Article Title: Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM
    Article Snippet: After incubating compound in PBS for 90 min at room temperature, the Nephelometric turbidity units (NTUs) were measured with NEPHELOstar (BMG LABTECH, Cary, North Carolina).

    Article Title: Supplemental Information Biochemical and Structural Characterization of Selective Allosteric Inhibitors of the Plasmodium falciparum Drug Target, Prolyl-tRNA-synthetase. Authors:
    Article Snippet: Triplicate aliquots were transferred to a flat bottomed polystyrene plate which was immediately read on the NEPHELOstar (BMG Lab Technologies).

    Incubation:

    Article Title: Applying nephelometry for analyzing liquid yeast cultures
    Article Snippet: .. The measurement, incubation, and shaking were performed fully automatically using Nephelostar (BMG LABTECH). ..



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    (A) Spores of B. cinerea were grown in PDB with 1/10 dilution of different ddH 2 O AWF extracts (mAWF, iAWF) in 96-wells microplates. Growth represented by the OD 635nm was monitored every 15 min for 48 h in a <t>nephelometric</t> reader. The average growth rates were calculated during the exponential phase. Results are represented as the mean percentage of growth compared to the control condition (PDB, 100%). Experiments were repeated three times with four different biological AWF replicates. A two-sample t-test was performed (*p<0.05). (B) H 2 O 2 production by B. cinerea following growth in mAWF and iAWF extracts compared to control conditions (PDB). At the end of the growth inhibition assay, each well of the microplate, was subjected to DAB staining to reveal H 2 O 2 production. Two staining controls without the fungus were performed with either PDB + DAB, as a negative control, or PDB + DAB + 5 mM H 2 O 2 + HRP (horseradish peroxidase) as a positive control. Experiments were repeated twice, and the same results were observed with four different biological replicas of AWF extracts.
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    (A) Spores of B. cinerea were grown in PDB with 1/10 dilution of different ddH 2 O AWF extracts (mAWF, iAWF) in 96-wells microplates. Growth represented by the OD 635nm was monitored every 15 min for 48 h in a <t>nephelometric</t> reader. The average growth rates were calculated during the exponential phase. Results are represented as the mean percentage of growth compared to the control condition (PDB, 100%). Experiments were repeated three times with four different biological AWF replicates. A two-sample t-test was performed (*p<0.05). (B) H 2 O 2 production by B. cinerea following growth in mAWF and iAWF extracts compared to control conditions (PDB). At the end of the growth inhibition assay, each well of the microplate, was subjected to DAB staining to reveal H 2 O 2 production. Two staining controls without the fungus were performed with either PDB + DAB, as a negative control, or PDB + DAB + 5 mM H 2 O 2 + HRP (horseradish peroxidase) as a positive control. Experiments were repeated twice, and the same results were observed with four different biological replicas of AWF extracts.
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    Image Search Results


    (A) Spores of B. cinerea were grown in PDB with 1/10 dilution of different ddH 2 O AWF extracts (mAWF, iAWF) in 96-wells microplates. Growth represented by the OD 635nm was monitored every 15 min for 48 h in a nephelometric reader. The average growth rates were calculated during the exponential phase. Results are represented as the mean percentage of growth compared to the control condition (PDB, 100%). Experiments were repeated three times with four different biological AWF replicates. A two-sample t-test was performed (*p<0.05). (B) H 2 O 2 production by B. cinerea following growth in mAWF and iAWF extracts compared to control conditions (PDB). At the end of the growth inhibition assay, each well of the microplate, was subjected to DAB staining to reveal H 2 O 2 production. Two staining controls without the fungus were performed with either PDB + DAB, as a negative control, or PDB + DAB + 5 mM H 2 O 2 + HRP (horseradish peroxidase) as a positive control. Experiments were repeated twice, and the same results were observed with four different biological replicas of AWF extracts.

    Journal: bioRxiv

    Article Title: Apoplast multi-omics profiling during fungal infection uncovers new players of basal and early induced immunity

    doi: 10.64898/2026.01.28.702280

    Figure Lengend Snippet: (A) Spores of B. cinerea were grown in PDB with 1/10 dilution of different ddH 2 O AWF extracts (mAWF, iAWF) in 96-wells microplates. Growth represented by the OD 635nm was monitored every 15 min for 48 h in a nephelometric reader. The average growth rates were calculated during the exponential phase. Results are represented as the mean percentage of growth compared to the control condition (PDB, 100%). Experiments were repeated three times with four different biological AWF replicates. A two-sample t-test was performed (*p<0.05). (B) H 2 O 2 production by B. cinerea following growth in mAWF and iAWF extracts compared to control conditions (PDB). At the end of the growth inhibition assay, each well of the microplate, was subjected to DAB staining to reveal H 2 O 2 production. Two staining controls without the fungus were performed with either PDB + DAB, as a negative control, or PDB + DAB + 5 mM H 2 O 2 + HRP (horseradish peroxidase) as a positive control. Experiments were repeated twice, and the same results were observed with four different biological replicas of AWF extracts.

    Article Snippet: Growth was automatically recorded each 15 minutes during 48h (193 cycles) using a nephelometric reader (NEPHELOstar Plus, BMG Labtech, Omega 5.70), equipped with a 635-nm laser as radiation source.

    Techniques: Control, Growth Inhibition Assay, Staining, Negative Control, Positive Control