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Carl Zeiss confocal laser scanning inverted microscope
Confocal Laser Scanning Inverted Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 88/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/confocal laser scanning inverted microscope/product/Carl Zeiss
Average 88 stars, based on 3 article reviews
Price from $9.99 to $1999.99
confocal laser scanning inverted microscope - by Bioz Stars, 2020-09
88/100 stars

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Related Articles

TUNEL Assay:

Article Title: Neuroprotective Effect of DAHP via Antiapoptosis in Cerebral Ischemia
Article Snippet: .. TUNEL-stained sections stained with DAPI were visualized with a confocal laser scanning inverted microscope (Meta Zeiss LSM 510). .. Immunohistochemistry 24 hours following reperfusion, animals were deeply anesthetized with 4% chloral hydrate and then perfused transcardially with 500 ml of 0.9% saline, followed by 4% paraformaldehyde in 0.01 M PBS.

Inverted Microscopy:

Article Title: Mechanically Induced Avoidance Response of Chloroplasts in Fern Protonemal Cells 1
Article Snippet: .. The specimens were observed under a confocal laser scanning inverted microscope (LSM 410, Zeiss). ..

Article Title: A New Protein-Protein Interaction Sensor Based on Tripartite Split-GFP Association
Article Snippet: .. Imaging of HEK cells was performed using a Zeiss (Carl Zeiss) confocal laser scanning inverted microscope (LSM 710 NLO with Quazar spectral detector array). .. Flow cytometry measurements were performed using a BD Biosciences FACSCalibur™ cytometer.

Article Title: Neuroprotective Effect of DAHP via Antiapoptosis in Cerebral Ischemia
Article Snippet: .. TUNEL-stained sections stained with DAPI were visualized with a confocal laser scanning inverted microscope (Meta Zeiss LSM 510). .. Immunohistochemistry 24 hours following reperfusion, animals were deeply anesthetized with 4% chloral hydrate and then perfused transcardially with 500 ml of 0.9% saline, followed by 4% paraformaldehyde in 0.01 M PBS.

Article Title: Deficiency of the DNA repair enzyme ATM in rheumatoid arthritis
Article Snippet: .. Images were acquired with a confocal laser-scanning inverted microscope (LSM 510 META Axiovert 200; Carl Zeiss, Inc.) ( ). .. siRNA transfection.

Article Title: Modulating Thiazole Orange Aggregation in Giant Lipid Vesicles: Photophysical Study Associated with FLIM and FCS
Article Snippet: .. For the FLIM studies, a confocal laser scanning inverted microscope (Axio Observer A1) from Zeiss was coupled with a DCS-120 system from Becker & Hickl GmbH (BH). ..

Article Title: Current automated 3D cell detection methods are not a suitable replacement for manual stereologic cell counting
Article Snippet: .. In the image data set investigated by Chinta and Wasser ( )—live Drosophila embryos expressing histone-2Av-green fluorescence protein imaged with a confocal laser scanning inverted microscope (Zeiss 5 Live; Carl Zeiss, Jena, Germany) and a 63×/1.4 oil DIC Plan-Apochromat objective—the use of FARSIGHT resulted in slight oversegmentation, supposedly related to increased seed detection due to spatially distinct clusters of condensed chromatin (Chinta and Wasser, ). ..

Article Title: DNA-dependent protein kinase catalytic subunit mediates T-cell loss in rheumatoid arthritis
Article Snippet: .. Images were acquired with a confocal laser-scanning inverted microscope (LSM 510 META Axiovert 200; Carl Zeiss, Inc.). ..

Fluorescence:

Article Title: Current automated 3D cell detection methods are not a suitable replacement for manual stereologic cell counting
Article Snippet: .. In the image data set investigated by Chinta and Wasser ( )—live Drosophila embryos expressing histone-2Av-green fluorescence protein imaged with a confocal laser scanning inverted microscope (Zeiss 5 Live; Carl Zeiss, Jena, Germany) and a 63×/1.4 oil DIC Plan-Apochromat objective—the use of FARSIGHT resulted in slight oversegmentation, supposedly related to increased seed detection due to spatially distinct clusters of condensed chromatin (Chinta and Wasser, ). ..

Imaging:

Article Title: A New Protein-Protein Interaction Sensor Based on Tripartite Split-GFP Association
Article Snippet: .. Imaging of HEK cells was performed using a Zeiss (Carl Zeiss) confocal laser scanning inverted microscope (LSM 710 NLO with Quazar spectral detector array). .. Flow cytometry measurements were performed using a BD Biosciences FACSCalibur™ cytometer.

Expressing:

Article Title: Current automated 3D cell detection methods are not a suitable replacement for manual stereologic cell counting
Article Snippet: .. In the image data set investigated by Chinta and Wasser ( )—live Drosophila embryos expressing histone-2Av-green fluorescence protein imaged with a confocal laser scanning inverted microscope (Zeiss 5 Live; Carl Zeiss, Jena, Germany) and a 63×/1.4 oil DIC Plan-Apochromat objective—the use of FARSIGHT resulted in slight oversegmentation, supposedly related to increased seed detection due to spatially distinct clusters of condensed chromatin (Chinta and Wasser, ). ..

Staining:

Article Title: Neuroprotective Effect of DAHP via Antiapoptosis in Cerebral Ischemia
Article Snippet: .. TUNEL-stained sections stained with DAPI were visualized with a confocal laser scanning inverted microscope (Meta Zeiss LSM 510). .. Immunohistochemistry 24 hours following reperfusion, animals were deeply anesthetized with 4% chloral hydrate and then perfused transcardially with 500 ml of 0.9% saline, followed by 4% paraformaldehyde in 0.01 M PBS.

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    Carl Zeiss confocal inverted laser scanning microscope
    The spatial distribution of actin in RBC ghosts revealed by fluorescent probes of phalloidin-rhodamine and DNase I–FITC. The spatial distribution of the fluorescent probes was analyzed via a three-dimensional optical sectioning by a <t>confocal</t> <t>inverted</t> <t>laser</t> <t>scanning</t> <t>microscope.</t> ( A ) Optical sections ( a–h , 0.6 μm apart) of RBC ghost labeled by phalloidin-rhodamine (4.4 μM). Each square of the gallery of images possesses a dimension of 9.5 μm × 9.5 μm. ( B ) The distribution of phalloidin-rhodamine and DNase I–FITC in RBC ghosts in an optical section taken at the middle (half thickness) of the RBC ghost. Inset , The separate distribution of phalloidin-rhodamine ( red ) and DNase I ( green ) in a RBC ghost that was labeled with both phalloidin-rhodamine and DNase I–FITC. Bars: ( A ) 5 μm; ( B ) 10 μm.
    Confocal Inverted Laser Scanning Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 80/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/confocal inverted laser scanning microscope/product/Carl Zeiss
    Average 80 stars, based on 4 article reviews
    Price from $9.99 to $1999.99
    confocal inverted laser scanning microscope - by Bioz Stars, 2020-09
    80/100 stars
      Buy from Supplier

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    The spatial distribution of actin in RBC ghosts revealed by fluorescent probes of phalloidin-rhodamine and DNase I–FITC. The spatial distribution of the fluorescent probes was analyzed via a three-dimensional optical sectioning by a confocal inverted laser scanning microscope. ( A ) Optical sections ( a–h , 0.6 μm apart) of RBC ghost labeled by phalloidin-rhodamine (4.4 μM). Each square of the gallery of images possesses a dimension of 9.5 μm × 9.5 μm. ( B ) The distribution of phalloidin-rhodamine and DNase I–FITC in RBC ghosts in an optical section taken at the middle (half thickness) of the RBC ghost. Inset , The separate distribution of phalloidin-rhodamine ( red ) and DNase I ( green ) in a RBC ghost that was labeled with both phalloidin-rhodamine and DNase I–FITC. Bars: ( A ) 5 μm; ( B ) 10 μm.

    Journal: The Journal of Cell Biology

    Article Title: Mechanical Fluctuations of the Membrane-Skeleton Are Dependent on F-Actin ATPase in Human Erythrocytes

    doi:

    Figure Lengend Snippet: The spatial distribution of actin in RBC ghosts revealed by fluorescent probes of phalloidin-rhodamine and DNase I–FITC. The spatial distribution of the fluorescent probes was analyzed via a three-dimensional optical sectioning by a confocal inverted laser scanning microscope. ( A ) Optical sections ( a–h , 0.6 μm apart) of RBC ghost labeled by phalloidin-rhodamine (4.4 μM). Each square of the gallery of images possesses a dimension of 9.5 μm × 9.5 μm. ( B ) The distribution of phalloidin-rhodamine and DNase I–FITC in RBC ghosts in an optical section taken at the middle (half thickness) of the RBC ghost. Inset , The separate distribution of phalloidin-rhodamine ( red ) and DNase I ( green ) in a RBC ghost that was labeled with both phalloidin-rhodamine and DNase I–FITC. Bars: ( A ) 5 μm; ( B ) 10 μm.

    Article Snippet: The spatial distribution of the fluorescent probes was analyzed via a three-dimensional optical sectioning using a confocal inverted laser scanning microscope (LSM 410; Carl Zeiss Inc. , Thornwood, NY).

    Techniques: Laser-Scanning Microscopy, Labeling