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Carl Zeiss axioimager a1 upright microscope
Axioimager A1 Upright Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 99/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/axioimager a1 upright microscope/product/Carl Zeiss
Average 99 stars, based on 15 article reviews
Price from $9.99 to $1999.99
axioimager a1 upright microscope - by Bioz Stars, 2020-11
99/100 stars

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Related Articles

Immunocytochemistry:

Article Title: Glioblastoma Tissue Slice Tandem-Cultures for Quantitative Evaluation of Inhibitory Effects on Invasion and Growth
Article Snippet: .. Microscopic pictures were taken with a Zeiss Axioskop upright microscope, equipped with a Zeiss AxioCam ICc 1 camera (Carl Zeiss, Jena, Germany) and analyzed using the FIJI distribution of the ImageJ software suite and the FigureJ plugin. ..

Fluorescence:

Article Title: AAV2-BDNF promotes respiratory axon plasticity and recovery of diaphragm function following spinal cord injury
Article Snippet: .. GFP fluorescence histogram All images for analysis were taken in 30-μm sections using a Zeiss upright epifluorescence microscope (Carl Zeiss, Oberkochen, Germany) at ×10 and stitched together using Metamorph software (RRID:SCR_002368; Molecular Devices, San Jose, CA, USA). ..

Microscopy:

Article Title: AAV2-BDNF promotes respiratory axon plasticity and recovery of diaphragm function following spinal cord injury
Article Snippet: .. GFP fluorescence histogram All images for analysis were taken in 30-μm sections using a Zeiss upright epifluorescence microscope (Carl Zeiss, Oberkochen, Germany) at ×10 and stitched together using Metamorph software (RRID:SCR_002368; Molecular Devices, San Jose, CA, USA). ..

Article Title: Encoding of environmental cues in central amygdala neurons during foraging
Article Snippet: .. MicroscopyEpifluorescence images were obtained with an upright epifluorescence microscope (Zeiss) with 5×/0.15 or 10×/0.3 objectives (Zeiss). .. Images were minimally processed with ImageJ software (NIH) to adjust for brightness and contrast for optimal representation of the data.

Article Title: AAV2-BDNF promotes respiratory axon plasticity and recovery of diaphragm function following spinal cord injury
Article Snippet: .. PhMN soma size All images for analysis were taken in 30-μm sections using a Zeiss upright epifluorescence microscope at ×10 and stitched together using MetaMorph software. ..

Article Title: Single-Molecule Insights into ATP-Dependent Conformational Dynamics of Nucleoprotein Filaments of Deinococcus radiodurans RecA
Article Snippet: .. Optical Tweezers SetupA custom dual-trap optical tweezers setup built around an upright fluorescent microscope (AxioImager.Z1, Carl Zeiss, Oberkochen, Germany) was used as described previously [ , ]. .. In brief, a ND:YVO4 1064 nm laser beam (Spectra-Physics, Mountain View, CA, USA) was split in two using a polarizing beam splitter cube and focused with an oil immersion lens (LOMO 100X, NA 1.32, St. Petersburg, Russia) to generate two orthogonally polarized optical traps.

Article Title: Low skeletal muscle capillarization limits muscle adaptation to resistance exercise training in older adults
Article Snippet: .. Images were captured at 20x magnification with a Zeiss upright microscope (AxioImager M1;Zeiss,Oberkochen,Germany) and analysis completed using the AxioVision Rel software (v4.9). ..

Article Title: Cell shape regulates global histone acetylation in human mammary epithelial cells
Article Snippet: .. Stained samples were imaged using a Spot RT camera attached to a Zeiss upright epifluorescence microscope or a Stanford Photonics XR/Mega-10 ICCD camera attached to a Zeiss spinning disk confocal microscope. .. DNA was stained with DAPI and the corresponding fluorescence was measured by acquiring confocal sections separated by 0.16 μm using a spinning disk confocal microscope.

Article Title: Glioblastoma Tissue Slice Tandem-Cultures for Quantitative Evaluation of Inhibitory Effects on Invasion and Growth
Article Snippet: .. Microscopic pictures were taken with a Zeiss Axioskop upright microscope, equipped with a Zeiss AxioCam ICc 1 camera (Carl Zeiss, Jena, Germany) and analyzed using the FIJI distribution of the ImageJ software suite and the FigureJ plugin. ..

Article Title: Ablation of striatal somatostatin interneurons affects MSN morphology and electrophysiological properties, and increases cocaine-induced hyperlocomotion in mice.
Article Snippet: .. The visual identification of MSNs from SST-Cre-/- iDTR+/- and SST-Cre+/- iDTR+/- mice was made with a 63x water-immersion objective of a Zeiss upright microscope (Axioskop 2FS Plus; Zeiss, Germany). ..

Mouse Assay:

Article Title: Ablation of striatal somatostatin interneurons affects MSN morphology and electrophysiological properties, and increases cocaine-induced hyperlocomotion in mice.
Article Snippet: .. The visual identification of MSNs from SST-Cre-/- iDTR+/- and SST-Cre+/- iDTR+/- mice was made with a 63x water-immersion objective of a Zeiss upright microscope (Axioskop 2FS Plus; Zeiss, Germany). ..

Staining:

Article Title: Cell shape regulates global histone acetylation in human mammary epithelial cells
Article Snippet: .. Stained samples were imaged using a Spot RT camera attached to a Zeiss upright epifluorescence microscope or a Stanford Photonics XR/Mega-10 ICCD camera attached to a Zeiss spinning disk confocal microscope. .. DNA was stained with DAPI and the corresponding fluorescence was measured by acquiring confocal sections separated by 0.16 μm using a spinning disk confocal microscope.

Software:

Article Title: AAV2-BDNF promotes respiratory axon plasticity and recovery of diaphragm function following spinal cord injury
Article Snippet: .. GFP fluorescence histogram All images for analysis were taken in 30-μm sections using a Zeiss upright epifluorescence microscope (Carl Zeiss, Oberkochen, Germany) at ×10 and stitched together using Metamorph software (RRID:SCR_002368; Molecular Devices, San Jose, CA, USA). ..

Article Title: AAV2-BDNF promotes respiratory axon plasticity and recovery of diaphragm function following spinal cord injury
Article Snippet: .. PhMN soma size All images for analysis were taken in 30-μm sections using a Zeiss upright epifluorescence microscope at ×10 and stitched together using MetaMorph software. ..

Article Title: Low skeletal muscle capillarization limits muscle adaptation to resistance exercise training in older adults
Article Snippet: .. Images were captured at 20x magnification with a Zeiss upright microscope (AxioImager M1;Zeiss,Oberkochen,Germany) and analysis completed using the AxioVision Rel software (v4.9). ..

Article Title: Glioblastoma Tissue Slice Tandem-Cultures for Quantitative Evaluation of Inhibitory Effects on Invasion and Growth
Article Snippet: .. Microscopic pictures were taken with a Zeiss Axioskop upright microscope, equipped with a Zeiss AxioCam ICc 1 camera (Carl Zeiss, Jena, Germany) and analyzed using the FIJI distribution of the ImageJ software suite and the FigureJ plugin. ..

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  • 88
    Carl Zeiss axioimager a1 upright epifluorescent microscope
    The FANCD2 NLS mutants fail to correct the ICL sensitivity of FA-D2 patient cells. ( A ) FA-D2 cells stably expressing LacZ, FANCD2-WT, FANCD2-∆N57, FANCD2-∆N100, FANCD2-3N, or FANCD2-K561R were incubated in the absence or presence of 8 or 16 nM MMC for 24 h and the numbers of chromosome aberrations including gaps and breaks, dicentrics, and complex chromosome aberrations, including radial formations, were scored. Metaphase spreads were analyzed using a Zeiss <t>AxioImager.A1</t> upright <t>epifluorescent</t> microscope with AxioVision LE 4.6 image acquisition software. At least 80 metaphases were scored per treatment. Error bars represent the standard error of the means. ( B ) FA-D2 cells stably expressing LacZ, FANCD2-WT and FANCD2-∆N57 were incubated in the absence (NT) or presence of 40 nM MMC for 18 h, and allowed to recover for 0, 4.5 or 7 h. Cells were then fixed, stained with rabbit polyclonal anti-DNA-PK CS pS2056, and counterstained with DAPI. At least 300 cells were scored for nuclei with > 5 DNA-PK CS foci. Error bars represent the standard error of the means from two independent experiments. ***, p
    Axioimager A1 Upright Epifluorescent Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 88/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/axioimager a1 upright epifluorescent microscope/product/Carl Zeiss
    Average 88 stars, based on 15 article reviews
    Price from $9.99 to $1999.99
    axioimager a1 upright epifluorescent microscope - by Bioz Stars, 2020-11
    88/100 stars
      Buy from Supplier

    92
    Carl Zeiss axoexaminer a1 upright microscope
    The FANCD2 NLS mutants fail to correct the ICL sensitivity of FA-D2 patient cells. ( A ) FA-D2 cells stably expressing LacZ, FANCD2-WT, FANCD2-∆N57, FANCD2-∆N100, FANCD2-3N, or FANCD2-K561R were incubated in the absence or presence of 8 or 16 nM MMC for 24 h and the numbers of chromosome aberrations including gaps and breaks, dicentrics, and complex chromosome aberrations, including radial formations, were scored. Metaphase spreads were analyzed using a Zeiss <t>AxioImager.A1</t> upright <t>epifluorescent</t> microscope with AxioVision LE 4.6 image acquisition software. At least 80 metaphases were scored per treatment. Error bars represent the standard error of the means. ( B ) FA-D2 cells stably expressing LacZ, FANCD2-WT and FANCD2-∆N57 were incubated in the absence (NT) or presence of 40 nM MMC for 18 h, and allowed to recover for 0, 4.5 or 7 h. Cells were then fixed, stained with rabbit polyclonal anti-DNA-PK CS pS2056, and counterstained with DAPI. At least 300 cells were scored for nuclei with > 5 DNA-PK CS foci. Error bars represent the standard error of the means from two independent experiments. ***, p
    Axoexaminer A1 Upright Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 92/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/axoexaminer a1 upright microscope/product/Carl Zeiss
    Average 92 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    axoexaminer a1 upright microscope - by Bioz Stars, 2020-11
    92/100 stars
      Buy from Supplier

    92
    Carl Zeiss upright microscope
    The FANCD2 NLS mutants fail to correct the ICL sensitivity of FA-D2 patient cells. ( A ) FA-D2 cells stably expressing LacZ, FANCD2-WT, FANCD2-∆N57, FANCD2-∆N100, FANCD2-3N, or FANCD2-K561R were incubated in the absence or presence of 8 or 16 nM MMC for 24 h and the numbers of chromosome aberrations including gaps and breaks, dicentrics, and complex chromosome aberrations, including radial formations, were scored. Metaphase spreads were analyzed using a Zeiss <t>AxioImager.A1</t> upright <t>epifluorescent</t> microscope with AxioVision LE 4.6 image acquisition software. At least 80 metaphases were scored per treatment. Error bars represent the standard error of the means. ( B ) FA-D2 cells stably expressing LacZ, FANCD2-WT and FANCD2-∆N57 were incubated in the absence (NT) or presence of 40 nM MMC for 18 h, and allowed to recover for 0, 4.5 or 7 h. Cells were then fixed, stained with rabbit polyclonal anti-DNA-PK CS pS2056, and counterstained with DAPI. At least 300 cells were scored for nuclei with > 5 DNA-PK CS foci. Error bars represent the standard error of the means from two independent experiments. ***, p
    Upright Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 92/100, based on 1396 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/upright microscope/product/Carl Zeiss
    Average 92 stars, based on 1396 article reviews
    Price from $9.99 to $1999.99
    upright microscope - by Bioz Stars, 2020-11
    92/100 stars
      Buy from Supplier

    Image Search Results


    The FANCD2 NLS mutants fail to correct the ICL sensitivity of FA-D2 patient cells. ( A ) FA-D2 cells stably expressing LacZ, FANCD2-WT, FANCD2-∆N57, FANCD2-∆N100, FANCD2-3N, or FANCD2-K561R were incubated in the absence or presence of 8 or 16 nM MMC for 24 h and the numbers of chromosome aberrations including gaps and breaks, dicentrics, and complex chromosome aberrations, including radial formations, were scored. Metaphase spreads were analyzed using a Zeiss AxioImager.A1 upright epifluorescent microscope with AxioVision LE 4.6 image acquisition software. At least 80 metaphases were scored per treatment. Error bars represent the standard error of the means. ( B ) FA-D2 cells stably expressing LacZ, FANCD2-WT and FANCD2-∆N57 were incubated in the absence (NT) or presence of 40 nM MMC for 18 h, and allowed to recover for 0, 4.5 or 7 h. Cells were then fixed, stained with rabbit polyclonal anti-DNA-PK CS pS2056, and counterstained with DAPI. At least 300 cells were scored for nuclei with > 5 DNA-PK CS foci. Error bars represent the standard error of the means from two independent experiments. ***, p

    Journal: PLoS ONE

    Article Title: Coordinate Nuclear Targeting of the FANCD2 and FANCI Proteins via a FANCD2 Nuclear Localization Signal

    doi: 10.1371/journal.pone.0081387

    Figure Lengend Snippet: The FANCD2 NLS mutants fail to correct the ICL sensitivity of FA-D2 patient cells. ( A ) FA-D2 cells stably expressing LacZ, FANCD2-WT, FANCD2-∆N57, FANCD2-∆N100, FANCD2-3N, or FANCD2-K561R were incubated in the absence or presence of 8 or 16 nM MMC for 24 h and the numbers of chromosome aberrations including gaps and breaks, dicentrics, and complex chromosome aberrations, including radial formations, were scored. Metaphase spreads were analyzed using a Zeiss AxioImager.A1 upright epifluorescent microscope with AxioVision LE 4.6 image acquisition software. At least 80 metaphases were scored per treatment. Error bars represent the standard error of the means. ( B ) FA-D2 cells stably expressing LacZ, FANCD2-WT and FANCD2-∆N57 were incubated in the absence (NT) or presence of 40 nM MMC for 18 h, and allowed to recover for 0, 4.5 or 7 h. Cells were then fixed, stained with rabbit polyclonal anti-DNA-PK CS pS2056, and counterstained with DAPI. At least 300 cells were scored for nuclei with > 5 DNA-PK CS foci. Error bars represent the standard error of the means from two independent experiments. ***, p

    Article Snippet: Nuclear foci were analyzed using a Zeiss AxioImager.A1 upright epifluorescent microscope with AxioVision LE 4.6 image acquisition software.

    Techniques: Stable Transfection, Expressing, Incubation, Microscopy, Software, Staining