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postacquisition image processing  (Oxford Instruments)


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  • 99

    Structured Review

    Oxford Instruments postacquisition image processing
    Postacquisition Image Processing, supplied by Oxford Instruments, used in various techniques. Bioz Stars score: 99/100, based on 44185 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/postacquisition+processing+postacquisition+image+processing/Imaris/pm34313548-311-0-14
    Average 99 stars, based on 44185 article reviews
    postacquisition image processing - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Staining:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Imaging:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Generated:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Microscopy:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Fluorsave:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Software:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Incubation:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Fluorescence:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Mass Cytometry:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Cytometry:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr

    Protease Inhibitor:

    Article Title: Disrupted glial metabolism and myelin vulnerability in a mouse model of glucose transporter type 1 deficiency syndrome.
    Article Snippet: slipped using FluorSave TM reagent (Millipore). Imaging was performed using a NI-E Spinning disk microscope with a Nikon 20x objective. GFAP-, S100β-, OLIG2- and ASPA-positive cells were counted using Imaris software (version 10.2.0, Oxford Instruments) or ImageJ (version 1.53t) with automated, supervised counting. The number of positive cells was divided by the volume of striatum analyzed and expr



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