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lightcycler 96 well plates  (Roche)


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    Structured Review

    Roche lightcycler 96 well plates
    Lightcycler 96 Well Plates, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 10067 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lightcycler 96 well plates/product/Roche
    Average 99 stars, based on 10067 article reviews
    lightcycler 96 well plates - by Bioz Stars, 2026-02
    99/100 stars

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    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche <t>LightCycler</t> <t>480</t> System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.
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    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche <t>LightCycler</t> <t>480</t> System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.
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    Roche 96 well plates
    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche <t>LightCycler</t> <t>480</t> System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.
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    Roche well plate
    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche <t>LightCycler</t> <t>480</t> System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.
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    Roche well plate setting
    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche <t>LightCycler</t> <t>480</t> System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.
    Well Plate Setting, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/well plate setting/product/Roche
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    Image Search Results


    AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Journal: Biomedicines

    Article Title: Alzheimer’s Disease-Associated Molecular Abnormalities in White Matter Glia and Related Pathologies Detected in Unfractionated and O4-Selected Serum Exosomes Using a Liquid Biopsy Approach

    doi: 10.3390/biomedicines14010251

    Figure Lengend Snippet: AD effects on immature and non-myelinating oligodendrocyte glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) mRNA transcripts were measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) CNPase , ( B ) GALC , ( C ) PLP1 , and ( D ) PDGFR-α. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were analyzed by two-way ANOVA with post hoc Tukey multiple-comparison tests. Significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Article Snippet: Targeted arrays were constructed by spotting and drying primer pairs (10 pmol/10 μL) into individual wells of a Lightcycler 480 Multi-well Plate 96 (Roche, Indianapolis, IN, USA).

    Techniques: Expressing, Control, Quantitative RT-PCR, Comparison

    AD effects on mature oligodendrocyte/myelin glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) purified RNA was reverse-transcribed to generate cDNA, and gene expression was measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) MOG , ( B ) MAG , and ( C ) MBP. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were first analyzed by two-way ANOVA followed by post hoc Tukey multiple-comparison tests. The corresponding significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Journal: Biomedicines

    Article Title: Alzheimer’s Disease-Associated Molecular Abnormalities in White Matter Glia and Related Pathologies Detected in Unfractionated and O4-Selected Serum Exosomes Using a Liquid Biopsy Approach

    doi: 10.3390/biomedicines14010251

    Figure Lengend Snippet: AD effects on mature oligodendrocyte/myelin glycoprotein mRNA expression in frontal lobe white matter. Control (n = 8) and AD (n = 8) purified RNA was reverse-transcribed to generate cDNA, and gene expression was measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) MOG , ( B ) MAG , and ( C ) MBP. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were first analyzed by two-way ANOVA followed by post hoc Tukey multiple-comparison tests. The corresponding significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Article Snippet: Targeted arrays were constructed by spotting and drying primer pairs (10 pmol/10 μL) into individual wells of a Lightcycler 480 Multi-well Plate 96 (Roche, Indianapolis, IN, USA).

    Techniques: Expressing, Control, Purification, Reverse Transcription, Gene Expression, Quantitative RT-PCR, Comparison

    AD effects on expression of astrocytic mRNA transcripts in frontal lobe white matter. Control (n = 8) and AD (n = 8) purified RNA was reverse-transcribed to generate cDNA, and gene expression was measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) Nestin , ( B ) Vimentin , and ( C ) GFAP. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were first analyzed by two-way ANOVA followed by post hoc Tukey multiple-comparison tests. The corresponding significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Journal: Biomedicines

    Article Title: Alzheimer’s Disease-Associated Molecular Abnormalities in White Matter Glia and Related Pathologies Detected in Unfractionated and O4-Selected Serum Exosomes Using a Liquid Biopsy Approach

    doi: 10.3390/biomedicines14010251

    Figure Lengend Snippet: AD effects on expression of astrocytic mRNA transcripts in frontal lobe white matter. Control (n = 8) and AD (n = 8) purified RNA was reverse-transcribed to generate cDNA, and gene expression was measured by qRT-PCR using a Roche LightCycler 480 System. Violin plots (mean, quartiles, and range) display results corresponding to ( A ) Nestin , ( B ) Vimentin , and ( C ) GFAP. Relative mRNA abundance was calculated using the 2 −ΔΔCt method with results normalized to internal control genes. Data were first analyzed by two-way ANOVA followed by post hoc Tukey multiple-comparison tests. The corresponding significant ( p ≤ 0.05) differences are shown within the panels. See for the full gene names, PCR primer sequences, and gene functions.

    Article Snippet: Targeted arrays were constructed by spotting and drying primer pairs (10 pmol/10 μL) into individual wells of a Lightcycler 480 Multi-well Plate 96 (Roche, Indianapolis, IN, USA).

    Techniques: Expressing, Control, Purification, Reverse Transcription, Gene Expression, Quantitative RT-PCR, Comparison