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confocal image displayed on maximum intensity projection zeiss lsm880  (Carl Zeiss)


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    Carl Zeiss confocal image displayed on maximum intensity projection zeiss lsm880
    Confocal Image Displayed On Maximum Intensity Projection Zeiss Lsm880, supplied by Carl Zeiss, 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/maximum+intensity/pm40565279-53-5-7?v=Carl+Zeiss
    Average 90 stars, based on 1 article reviews
    confocal image displayed on maximum intensity projection zeiss lsm880 - by Bioz Stars, 2026-08
    90/100 stars

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    Lesions identified for animal 40884 using Invicro VivoQuant ( Ai and B ) <t>or</t> <t>Imaris</t> ( Aii and C ) at different time points and different views. A : 3D view of lesions at 18 weeks post-infection in Invicro VivoQuant (i) and the same lesions in Imaris (ii) . B-C : Slice views of lesions identified with Invicro VivoQuant ( B ) or Imaris ( C ) at 6 (i, iv) , 14 (ii, v) , and 18 (iii, vi) weeks post-infection in both sagittal (i-iii) and coronal (iv-vi) slice views (see also and ). <t>PET</t> signal associated with the heart (shown by an arrow in Ai-ii ) was excluded from our analyses.
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    Image Search Results


    Lesions identified for animal 40884 using Invicro VivoQuant ( Ai and B ) or Imaris ( Aii and C ) at different time points and different views. A : 3D view of lesions at 18 weeks post-infection in Invicro VivoQuant (i) and the same lesions in Imaris (ii) . B-C : Slice views of lesions identified with Invicro VivoQuant ( B ) or Imaris ( C ) at 6 (i, iv) , 14 (ii, v) , and 18 (iii, vi) weeks post-infection in both sagittal (i-iii) and coronal (iv-vi) slice views (see also and ). PET signal associated with the heart (shown by an arrow in Ai-ii ) was excluded from our analyses.

    Journal: bioRxiv

    Article Title: Using Imaris to rigorously track PET-defined sites of lung inflammation in Mycobacterium tuberculosis -exposed non-human primates

    doi: 10.1101/2025.07.04.663191

    Figure Lengend Snippet: Lesions identified for animal 40884 using Invicro VivoQuant ( Ai and B ) or Imaris ( Aii and C ) at different time points and different views. A : 3D view of lesions at 18 weeks post-infection in Invicro VivoQuant (i) and the same lesions in Imaris (ii) . B-C : Slice views of lesions identified with Invicro VivoQuant ( B ) or Imaris ( C ) at 6 (i, iv) , 14 (ii, v) , and 18 (iii, vi) weeks post-infection in both sagittal (i-iii) and coronal (iv-vi) slice views (see also and ). PET signal associated with the heart (shown by an arrow in Ai-ii ) was excluded from our analyses.

    Article Snippet: We therefore investigated if simply using actual maximum PET channel intensity, provided by Imaris for individual lesions, may nevertheless provide important information.

    Techniques: Infection

    We illustrate how PET/CT scans are typically analyzed with Invicro VivoQuant, the standard proprietary packages for PET/CT data analysis ( A ), and with Imaris, proprietary packages typically used for fluorescent microscopy data analysis ( B ). A : With Invicro VivoQuant (i-iv) , the operator analyzes reconstructed 3D images by using 2D slices and manually labeling contours of the lesions, defined by PET signal. Invicro VivoQuant then provides various SUV characteristics, such as max SUV, for ether individual lesions or the whole lung. B : With Imaris (i-vi) , PET/CT DICOM files are imported as 2-channel images, and scans done at different times can be incorporated into the same Imaris file by adding new time frames. Then scans for different time points are aligned using “Correct for drift” routine by using landmarks (6 locations of spine vertebra). Then region of interest ( ROI ) is then identified around each suspected lesion and the data in ROI is processed using 3D routine “Surfaces”. All lesions then can be grouped into the specific group depending on the location of the lesion (e.g., lung vs. lymph nodes).

    Journal: bioRxiv

    Article Title: Using Imaris to rigorously track PET-defined sites of lung inflammation in Mycobacterium tuberculosis -exposed non-human primates

    doi: 10.1101/2025.07.04.663191

    Figure Lengend Snippet: We illustrate how PET/CT scans are typically analyzed with Invicro VivoQuant, the standard proprietary packages for PET/CT data analysis ( A ), and with Imaris, proprietary packages typically used for fluorescent microscopy data analysis ( B ). A : With Invicro VivoQuant (i-iv) , the operator analyzes reconstructed 3D images by using 2D slices and manually labeling contours of the lesions, defined by PET signal. Invicro VivoQuant then provides various SUV characteristics, such as max SUV, for ether individual lesions or the whole lung. B : With Imaris (i-vi) , PET/CT DICOM files are imported as 2-channel images, and scans done at different times can be incorporated into the same Imaris file by adding new time frames. Then scans for different time points are aligned using “Correct for drift” routine by using landmarks (6 locations of spine vertebra). Then region of interest ( ROI ) is then identified around each suspected lesion and the data in ROI is processed using 3D routine “Surfaces”. All lesions then can be grouped into the specific group depending on the location of the lesion (e.g., lung vs. lymph nodes).

    Article Snippet: We therefore investigated if simply using actual maximum PET channel intensity, provided by Imaris for individual lesions, may nevertheless provide important information.

    Techniques: Positron Emission Tomography-Computed Tomography, Microscopy, Labeling

    We analyzed PET/CT data from four Mtb-infected RMs (each with three PET/CT scans) either with Invicro VivoQuant, a standard software for PET/CT data analysis, or Imaris (Bitplane), software typically used for analysis of fluorescent microscopy data. For each lesion we plot maximum SUV as provided by Invicro VivoQuant (x axes) or maximum intensity as provided by Imaris (y axes), normalized using weight of the animal and 18F-FDG injection dose and multiplied by f = 10 (see ). We show data for animal 41883 ( A ), 44104 ( B ), 41634 ( C ), and 40884 ( D ) with n indicating the number of lesions detected in all scans and m being a regression slope between SUV values of Invicro VivoQuant vs. Imaris for all lesions or lesions found in individual scans; we show the regression lines in individual panels for all lesions. Scans done at different times are shown by different color intensity. The dashed line shows the slope of 1.

    Journal: bioRxiv

    Article Title: Using Imaris to rigorously track PET-defined sites of lung inflammation in Mycobacterium tuberculosis -exposed non-human primates

    doi: 10.1101/2025.07.04.663191

    Figure Lengend Snippet: We analyzed PET/CT data from four Mtb-infected RMs (each with three PET/CT scans) either with Invicro VivoQuant, a standard software for PET/CT data analysis, or Imaris (Bitplane), software typically used for analysis of fluorescent microscopy data. For each lesion we plot maximum SUV as provided by Invicro VivoQuant (x axes) or maximum intensity as provided by Imaris (y axes), normalized using weight of the animal and 18F-FDG injection dose and multiplied by f = 10 (see ). We show data for animal 41883 ( A ), 44104 ( B ), 41634 ( C ), and 40884 ( D ) with n indicating the number of lesions detected in all scans and m being a regression slope between SUV values of Invicro VivoQuant vs. Imaris for all lesions or lesions found in individual scans; we show the regression lines in individual panels for all lesions. Scans done at different times are shown by different color intensity. The dashed line shows the slope of 1.

    Article Snippet: We therefore investigated if simply using actual maximum PET channel intensity, provided by Imaris for individual lesions, may nevertheless provide important information.

    Techniques: Positron Emission Tomography-Computed Tomography, Infection, Software, Microscopy, Injection

    By using XYZ coordinates, provided by Imaris we plotted individual lesions detected in animals 41883 ( A ), 44104 ( B ), 41634 ( C ), and 40884 ( D ) at different time points after infection (times are denoted on individual panels). Note that the plots are from rear view of the animals (see also ). We also s how the total number of lesions detected at each time point as n . Lesions are plotted as spheres with the radius R = V/ (4 π ) where V is the PET volume determined by Imaris . Intensity of the color denotes scaled maximum PET signal intensity normalized to I max values for the largest maximum intensity for all lesions in all scans of a given animal; this also takes into account the actual injected FDG dose and weight of the animal . Black colors indicate animals that were asymptomatic and red colors indicate that the animal was diagnosed with active disease (TB).

    Journal: bioRxiv

    Article Title: Using Imaris to rigorously track PET-defined sites of lung inflammation in Mycobacterium tuberculosis -exposed non-human primates

    doi: 10.1101/2025.07.04.663191

    Figure Lengend Snippet: By using XYZ coordinates, provided by Imaris we plotted individual lesions detected in animals 41883 ( A ), 44104 ( B ), 41634 ( C ), and 40884 ( D ) at different time points after infection (times are denoted on individual panels). Note that the plots are from rear view of the animals (see also ). We also s how the total number of lesions detected at each time point as n . Lesions are plotted as spheres with the radius R = V/ (4 π ) where V is the PET volume determined by Imaris . Intensity of the color denotes scaled maximum PET signal intensity normalized to I max values for the largest maximum intensity for all lesions in all scans of a given animal; this also takes into account the actual injected FDG dose and weight of the animal . Black colors indicate animals that were asymptomatic and red colors indicate that the animal was diagnosed with active disease (TB).

    Article Snippet: We therefore investigated if simply using actual maximum PET channel intensity, provided by Imaris for individual lesions, may nevertheless provide important information.

    Techniques: Infection, Injection