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axio observer upright lsm 780 confocal microscope  (Carl Zeiss)


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    Carl Zeiss axio observer upright lsm 780 confocal microscope
    Axio Observer Upright Lsm 780 Confocal Microscope, supplied by Carl Zeiss, 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/product/axio+780+upright+microscope/pm36182026-85-6-5?v=Carl+Zeiss
    Average 99 stars, based on 1 article reviews
    axio observer upright lsm 780 confocal microscope - by Bioz Stars, 2026-07
    99/100 stars

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    Image Search Results


    Choices in image processing alter the final ratio image, especially at its edge. The position of a nucleus (yellow) in a M. truncatula root hair is shown in the bright field image of the root hair (grey), merged with the YFP image. Path A shows what happens when images are not processed, while Path B attempts to follow the image processing steps reported in Sieberer et al. . The 2D microscope image of the YFP and CFP intensities at the nucleus reflects the 3D structure of the nucleus, I 1 and I 2 B . The ratios YFP/CFP of images are I 2 A and I 3 B . We used the nuclear localised Ca 2 + sensor YC2.1.

    Journal: International Journal of Molecular Sciences

    Article Title: What Drives Symbiotic Calcium Signalling in Legumes? Insights and Challenges of Imaging

    doi: 10.3390/ijms20092245

    Figure Lengend Snippet: Choices in image processing alter the final ratio image, especially at its edge. The position of a nucleus (yellow) in a M. truncatula root hair is shown in the bright field image of the root hair (grey), merged with the YFP image. Path A shows what happens when images are not processed, while Path B attempts to follow the image processing steps reported in Sieberer et al. . The 2D microscope image of the YFP and CFP intensities at the nucleus reflects the 3D structure of the nucleus, I 1 and I 2 B . The ratios YFP/CFP of images are I 2 A and I 3 B . We used the nuclear localised Ca 2 + sensor YC2.1.

    Article Snippet: We imaged the root hairs using a confocal microscope (Zeiss Axio Imager Z2 upright microscope, LSM 780), and as Ca 2 + sensors, we used members of the Yellow cameleon (YC) family of genetically-encoded calcium sensors, specifically YC2.1 (Figures 4 and 5) and YC3.6 (Figures 6 and 8).

    Techniques: Microscopy

    Choices in image processing alter the final ratio image, especially at its edge. The position of a nucleus (yellow) in a M. truncatula root hair is shown in the bright field image of the root hair (grey), merged with the YFP image. The path A shows what happens when images are not processed, while the path B attempts to follow the image processing steps reported in Sieberer et al . The 2D microscope image of the YFP and CFP intensities at the nucleus reflects the 3D structure of the nucleus, I 1 and I 2 B . The ratio YFP/CFP images are I 2 A and I 3 B . We use the nuclear localised Ca 2+ sensor YC2.1.

    Journal: bioRxiv

    Article Title: What Drives Symbiotic Calcium Signalling In Legumes? Insights And Challenges Of Imaging

    doi: 10.1101/559971

    Figure Lengend Snippet: Choices in image processing alter the final ratio image, especially at its edge. The position of a nucleus (yellow) in a M. truncatula root hair is shown in the bright field image of the root hair (grey), merged with the YFP image. The path A shows what happens when images are not processed, while the path B attempts to follow the image processing steps reported in Sieberer et al . The 2D microscope image of the YFP and CFP intensities at the nucleus reflects the 3D structure of the nucleus, I 1 and I 2 B . The ratio YFP/CFP images are I 2 A and I 3 B . We use the nuclear localised Ca 2+ sensor YC2.1.

    Article Snippet: We imaged the root hairs using a confocal microscope (Zeiss Axio Imager Z2 upright microscope, LSM 780) and, as Ca 2+ sensors, we used members of the yellow cameleon (YC) family of genetically-encoded calcium sensors, specifically YC2.1 ( and ) and YC3.6 ( and ).

    Techniques: Microscopy