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fluorescent cool white light intensity equal to 100 µmol·photons·m–2·s−1  (Osram Sylvania)

 
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    Osram Sylvania fluorescent cool white light intensity equal to 100 µmol·photons·m–2·s−1
    Fluorescent Cool White Light Intensity Equal To 100 µmol·Photons·M–2·S−1, supplied by Osram Sylvania, 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/fluorescent+light+intensity/fluorescent+cool+white+light+intensity+equal+to+100+%C2%B5mol%C2%B7photons%C2%B7m+2%C2%B7s+1/10__3390_slash_en14051340-60-19-22
    Average 90 stars, based on 1 article reviews
    fluorescent cool white light intensity equal to 100 µmol·photons·m–2·s−1 - by Bioz Stars, 2026-10
    90/100 stars

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    other:

    Article Title: Mass spore production and inoculation of Calonectria pteridis on Eucalyptus spp. under different environmental conditions
    Article Snippet: Mycelial growth at different temperatures A 5-mm-diameter mycelial plug of LPF059 was transferred to the center of Petri dishes containing 30 mL of GAA and the plates were maintained at 5, 10, 15, 20, 25, 30, 35 or 40°C under a 12-h photoperiod (39 μmol s-1m-2 fluorescent light intensity, Osram, 20W) in a completely randomized design with five replicates per temperature.



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    In vivo G FP expression analysis control of the native and mutated promoters of AmXLN2 , AmBXL2 and AmABF1 . ( a ) Schematic representation of the native promoters and their variants with deleted putative XlnR-binding sites: P XLN2 Δ:P XLN2 with 5′-GGCTGA-3′ deleted; P BXL2 Δ:P BXL2 with 5′-GGTTAA-3′ deleted; P ABF1 Δ:P ABF1 with 5′-GGCTAT-3′ deleted. ( b ) Relative <t>fluorescence</t> intensity, ( c ) relative <t>GFP</t> transcriptional level, and ( d ) bright-field and corresponding fluorescence images of the reporter strains. Three independent replicates were performed for the statistical analysis. ∗ P < 0.05,∗∗ P < 0.01, ns: no significance.
    Fluorescent Cool White Light Intensity Equal To 100 µmol·Photons·M–2·S−1, supplied by Osram Sylvania, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    cool white fluorescent light intensity  (Osram Sylvania)
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    In vivo G FP expression analysis control of the native and mutated promoters of AmXLN2 , AmBXL2 and AmABF1 . ( a ) Schematic representation of the native promoters and their variants with deleted putative XlnR-binding sites: P XLN2 Δ:P XLN2 with 5′-GGCTGA-3′ deleted; P BXL2 Δ:P BXL2 with 5′-GGTTAA-3′ deleted; P ABF1 Δ:P ABF1 with 5′-GGCTAT-3′ deleted. ( b ) Relative <t>fluorescence</t> intensity, ( c ) relative <t>GFP</t> transcriptional level, and ( d ) bright-field and corresponding fluorescence images of the reporter strains. Three independent replicates were performed for the statistical analysis. ∗ P < 0.05,∗∗ P < 0.01, ns: no significance.
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    Image Search Results


    In vivo G FP expression analysis control of the native and mutated promoters of AmXLN2 , AmBXL2 and AmABF1 . ( a ) Schematic representation of the native promoters and their variants with deleted putative XlnR-binding sites: P XLN2 Δ:P XLN2 with 5′-GGCTGA-3′ deleted; P BXL2 Δ:P BXL2 with 5′-GGTTAA-3′ deleted; P ABF1 Δ:P ABF1 with 5′-GGCTAT-3′ deleted. ( b ) Relative fluorescence intensity, ( c ) relative GFP transcriptional level, and ( d ) bright-field and corresponding fluorescence images of the reporter strains. Three independent replicates were performed for the statistical analysis. ∗ P < 0.05,∗∗ P < 0.01, ns: no significance.

    Journal: Synthetic and Systems Biotechnology

    Article Title: AmXlnR, a transcription factor involved in xylan degradation and pentose catabolism, enhances pullulan production from xylose in Aureobasidium melanogenum

    doi: 10.1016/j.synbio.2026.02.007

    Figure Lengend Snippet: In vivo G FP expression analysis control of the native and mutated promoters of AmXLN2 , AmBXL2 and AmABF1 . ( a ) Schematic representation of the native promoters and their variants with deleted putative XlnR-binding sites: P XLN2 Δ:P XLN2 with 5′-GGCTGA-3′ deleted; P BXL2 Δ:P BXL2 with 5′-GGTTAA-3′ deleted; P ABF1 Δ:P ABF1 with 5′-GGCTAT-3′ deleted. ( b ) Relative fluorescence intensity, ( c ) relative GFP transcriptional level, and ( d ) bright-field and corresponding fluorescence images of the reporter strains. Three independent replicates were performed for the statistical analysis. ∗ P < 0.05,∗∗ P < 0.01, ns: no significance.

    Article Snippet: GFP fluorescence intensity was visualized using an Olympus U-LH100HG fluorescent microscope and quantified using a BioTeK Synergy H1 Hybrid Reader (BioTek Instruments Inc., USA) (485 nm excitation and 520 nm emission).

    Techniques: In Vivo, Expressing, Control, Binding Assay, Fluorescence