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Carl Zeiss lsm 510 model
Lsm 510 Model, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lsm 510 model/product/Carl Zeiss
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
lsm 510 model - by Bioz Stars, 2021-05
86/100 stars

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Article Title: Physio-Genetic Dissection of Dark-Induced Leaf Senescence and Timing Its Reversal in Barley 1Physio-Genetic Dissection of Dark-Induced Leaf Senescence and Timing Its Reversal in Barley 1 [OPEN]
Article Snippet: From the same samples, semithin sections were collected and observed microscopically (the Zeiss LSM 510 model, Axioverd 200 M).

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  • 99
    Carl Zeiss confocal laser scanning microscope
    Effect of 1/4MIC of 6a and N , O acetal naphthoquinone derivatives 7a , 7b , and 7c on biofilm development. ( A ) Biofilm formed on surfaces and stained with crystal violet. ( B ) <t>Confocal</t> <t>laser</t> <t>scanning</t> microscopy (CLSM). Effects of 1/4MIC of the derivatives 7b (32 µg/mL) and 7c (16 µg/mL) on biofilm formed by the MRSA strain BMB9393, compared with the untreated biofilm (C neg ). Van vancomycin (1/4 MIC; 0.5 µg/mL). NS not significant; ** p value
    Confocal Laser Scanning 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/result/confocal laser scanning microscope/product/Carl Zeiss
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    confocal laser scanning microscope - by Bioz Stars, 2021-05
    99/100 stars
      Buy from Supplier

    97
    Carl Zeiss model lsm510 laser scanning system
    Detection of GFP-L2 fusion protein bound to HeLa cells by fluorescence. (A) Phase-contrast microscopy of a HeLa cell cultured in a spinner flask. HeLa cells cultured in a spinner flask were incubated with GFP-L2(108–126) at 4°C for 1 h (B) and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (C). (B and C) The section near the center of a round cell cultured in suspension is presented. HeLa cells cultured on a glass slide were incubated with plain GFP at 4°C for 1 h (D), with GFP-L2(108–126) at 4°C for 1 h (E), and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (F). (E) The section near the surfaces of flat cells showed fluorescent dots with parts of nuclei. (F) The section near the centers of cells showed cytoplasmic fluorescence. Fluorescence was examined with a Carl Zeiss <t>LSM510</t> laser scanning confocal system. (D, E, and F) Nuclei were stained with propidium iodide.
    Model Lsm510 Laser Scanning System, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/model lsm510 laser scanning system/product/Carl Zeiss
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    model lsm510 laser scanning system - by Bioz Stars, 2021-05
    97/100 stars
      Buy from Supplier

    97
    Carl Zeiss confocal laser scanning fluorescence microscopy
    Enhancement of Aβ cellular uptake by RAP in brain vascular smooth muscle cells. The effect of RAP on the cellular uptake of Aβ in HBVSMC was analyzed using <t>confocal</t> <t>laser</t> <t>scanning</t> <t>microscopy.</t> HBVSMC were treated with 500 n m FAM-labeled
    Confocal Laser Scanning Fluorescence Microscopy, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/confocal laser scanning fluorescence microscopy/product/Carl Zeiss
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    confocal laser scanning fluorescence microscopy - by Bioz Stars, 2021-05
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    97
    Carl Zeiss laser scanning confocal microscope
    Effects of the sEphB4 injection on fluorescein leakage and CNV (choroidal neovascularization) lesion in rat. Fluorescein angiogram (FA) was performed 14 days after <t>laser</t> photocoagulation and intravitreal injection of the sEphB4. (A) Representative FA images in laser-induced rat (B) FA score: sEphB4 injection resulted in a dose dependent inhibition of fluorescein leakage CNV (20 FA images were pooled in each group). (C) Representative CNV lesions from PBS or different concentrations of sEphB4-HSA injection measured in FITC-labeled isolectin-B4 stained flat retinal mounts on day 14. (D) After being stained with isolectin B4, retinal flatmounts were visualized with a laser <t>scanning</t> <t>confocal</t> <t>microscope</t> Z stack images of CNV lesion were taken. The image stacks were rendered in 3D using velocity imaging software (Improvision Inc., Waltham, USA) and processed to digitally extract the fluorescent lesion volume. CNV volume was measured in micrometers cubed (14 images/each group), A dose dependent significant reduction of CNV volume was seen in EphB4-HSA treated rats compared with PBS (phosphate-buffered saline) injection.
    Laser Scanning Confocal Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/laser scanning confocal microscope/product/Carl Zeiss
    Average 97 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    laser scanning confocal microscope - by Bioz Stars, 2021-05
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    Image Search Results


    Effect of 1/4MIC of 6a and N , O acetal naphthoquinone derivatives 7a , 7b , and 7c on biofilm development. ( A ) Biofilm formed on surfaces and stained with crystal violet. ( B ) Confocal laser scanning microscopy (CLSM). Effects of 1/4MIC of the derivatives 7b (32 µg/mL) and 7c (16 µg/mL) on biofilm formed by the MRSA strain BMB9393, compared with the untreated biofilm (C neg ). Van vancomycin (1/4 MIC; 0.5 µg/mL). NS not significant; ** p value

    Journal: Scientific Reports

    Article Title: Antibiofilm effects of N,O-acetals derived from 2-amino-1,4-naphthoquinone are associated with downregulation of important global virulence regulators in methicillin-resistant Staphylococcus aureus

    doi: 10.1038/s41598-020-76372-z

    Figure Lengend Snippet: Effect of 1/4MIC of 6a and N , O acetal naphthoquinone derivatives 7a , 7b , and 7c on biofilm development. ( A ) Biofilm formed on surfaces and stained with crystal violet. ( B ) Confocal laser scanning microscopy (CLSM). Effects of 1/4MIC of the derivatives 7b (32 µg/mL) and 7c (16 µg/mL) on biofilm formed by the MRSA strain BMB9393, compared with the untreated biofilm (C neg ). Van vancomycin (1/4 MIC; 0.5 µg/mL). NS not significant; ** p value

    Article Snippet: Before visualization, SYTO 9 solution was removed and the material visualized using a confocal laser scanning microscope (Model LSM510 Carl Zeiss Meditec; Jena, Germany).

    Techniques: Staining, Confocal Laser Scanning Microscopy

    Detection of GFP-L2 fusion protein bound to HeLa cells by fluorescence. (A) Phase-contrast microscopy of a HeLa cell cultured in a spinner flask. HeLa cells cultured in a spinner flask were incubated with GFP-L2(108–126) at 4°C for 1 h (B) and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (C). (B and C) The section near the center of a round cell cultured in suspension is presented. HeLa cells cultured on a glass slide were incubated with plain GFP at 4°C for 1 h (D), with GFP-L2(108–126) at 4°C for 1 h (E), and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (F). (E) The section near the surfaces of flat cells showed fluorescent dots with parts of nuclei. (F) The section near the centers of cells showed cytoplasmic fluorescence. Fluorescence was examined with a Carl Zeiss LSM510 laser scanning confocal system. (D, E, and F) Nuclei were stained with propidium iodide.

    Journal: Journal of Virology

    Article Title: Human Papillomavirus Type 16 Minor Capsid Protein L2 N-Terminal Region Containing a Common Neutralization Epitope Binds to the Cell Surface and Enters the Cytoplasm

    doi: 10.1128/JVI.75.5.2331-2336.2001

    Figure Lengend Snippet: Detection of GFP-L2 fusion protein bound to HeLa cells by fluorescence. (A) Phase-contrast microscopy of a HeLa cell cultured in a spinner flask. HeLa cells cultured in a spinner flask were incubated with GFP-L2(108–126) at 4°C for 1 h (B) and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (C). (B and C) The section near the center of a round cell cultured in suspension is presented. HeLa cells cultured on a glass slide were incubated with plain GFP at 4°C for 1 h (D), with GFP-L2(108–126) at 4°C for 1 h (E), and with GFP-L2(108–126) at 4°C for 1 h and at 37°C for 4 h (F). (E) The section near the surfaces of flat cells showed fluorescent dots with parts of nuclei. (F) The section near the centers of cells showed cytoplasmic fluorescence. Fluorescence was examined with a Carl Zeiss LSM510 laser scanning confocal system. (D, E, and F) Nuclei were stained with propidium iodide.

    Article Snippet: Fluorescence was examined with a model LSM510 laser scanning system (Carl Zeiss Co. Ltd., Oberkochen, Germany).

    Techniques: Fluorescence, Microscopy, Cell Culture, Incubation, Staining

    Enhancement of Aβ cellular uptake by RAP in brain vascular smooth muscle cells. The effect of RAP on the cellular uptake of Aβ in HBVSMC was analyzed using confocal laser scanning microscopy. HBVSMC were treated with 500 n m FAM-labeled

    Journal:

    Article Title: Receptor-associated Protein Interacts with Amyloid-? Peptide and Promotes Its Cellular Uptake *

    doi: 10.1074/jbc.M109.015032

    Figure Lengend Snippet: Enhancement of Aβ cellular uptake by RAP in brain vascular smooth muscle cells. The effect of RAP on the cellular uptake of Aβ in HBVSMC was analyzed using confocal laser scanning microscopy. HBVSMC were treated with 500 n m FAM-labeled

    Article Snippet: After incubation with FAM-labeled Aβ40 (500 n m ) at 37 °C for 4 h in serum-free DMEM in the presence or absence of RAP (500 n m ), the fluorescence of Aβ40 was observed by confocal laser scanning fluorescence microscopy (Model LSM 510 inverted microscope, Carl Zeiss, Jena, Germany) at 488-nm argon excitation using a 510–535-nm bandpass barrier filter.

    Techniques: Confocal Laser Scanning Microscopy, Labeling

    Effects of the sEphB4 injection on fluorescein leakage and CNV (choroidal neovascularization) lesion in rat. Fluorescein angiogram (FA) was performed 14 days after laser photocoagulation and intravitreal injection of the sEphB4. (A) Representative FA images in laser-induced rat (B) FA score: sEphB4 injection resulted in a dose dependent inhibition of fluorescein leakage CNV (20 FA images were pooled in each group). (C) Representative CNV lesions from PBS or different concentrations of sEphB4-HSA injection measured in FITC-labeled isolectin-B4 stained flat retinal mounts on day 14. (D) After being stained with isolectin B4, retinal flatmounts were visualized with a laser scanning confocal microscope Z stack images of CNV lesion were taken. The image stacks were rendered in 3D using velocity imaging software (Improvision Inc., Waltham, USA) and processed to digitally extract the fluorescent lesion volume. CNV volume was measured in micrometers cubed (14 images/each group), A dose dependent significant reduction of CNV volume was seen in EphB4-HSA treated rats compared with PBS (phosphate-buffered saline) injection.

    Journal: Annals of Translational Medicine

    Article Title: Inhibition of laser induced rats choroidal neovascularization by intravitreous injection of sEphB4-HSA

    doi: 10.21037/atm-20-3810

    Figure Lengend Snippet: Effects of the sEphB4 injection on fluorescein leakage and CNV (choroidal neovascularization) lesion in rat. Fluorescein angiogram (FA) was performed 14 days after laser photocoagulation and intravitreal injection of the sEphB4. (A) Representative FA images in laser-induced rat (B) FA score: sEphB4 injection resulted in a dose dependent inhibition of fluorescein leakage CNV (20 FA images were pooled in each group). (C) Representative CNV lesions from PBS or different concentrations of sEphB4-HSA injection measured in FITC-labeled isolectin-B4 stained flat retinal mounts on day 14. (D) After being stained with isolectin B4, retinal flatmounts were visualized with a laser scanning confocal microscope Z stack images of CNV lesion were taken. The image stacks were rendered in 3D using velocity imaging software (Improvision Inc., Waltham, USA) and processed to digitally extract the fluorescent lesion volume. CNV volume was measured in micrometers cubed (14 images/each group), A dose dependent significant reduction of CNV volume was seen in EphB4-HSA treated rats compared with PBS (phosphate-buffered saline) injection.

    Article Snippet: The sections were cover-slipped (Vectashield medium; Vector Laboratories), and the lectin labeling was examined with the 20× objective of a laser scanning confocal microscope (LSM; model 510; Carl Zeiss Meditec, Dublin, CA).

    Techniques: Injection, Inhibition, Labeling, Staining, Microscopy, Imaging, Software