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63× objective  (Carl Zeiss)


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    Carl Zeiss 63× objective
    63× Objective, 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/track+objects+algorithm+metamorph+6%2E3/63+objective+%C3%97/pmc01665509-124-8-17
    Average 90 stars, based on 1 article reviews
    63× objective - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: A multicellular star-shaped actin network underpins epithelial organization and connectivity.
    Article Snippet: Dynamics experiments on live organoid-derived monolayers were performed on a live imaging setup on an inverted Zeiss microscope equipped with a CSU-X1 spinning disk head (Yokogawa–Andor), using Zeiss ×40 and ×63 objectives.

    Article Title: Green silver nanoparticles curcumin conjugate induced photodynamic therapy of lung cancer and lung cancer stem cells.
    Article Snippet: The stained cells were observed with the 63× objective of the Zeiss microscope (Carl Zeiss Microscopy GmbH, Jena, Germany) with the help of specic lters with different excitation (Ex) and emission (Em) wavelengths: Ex341/ Em452 nm for DAPI, Ex467/Em571 nm for Cum–PEG–BpAgNPs, Ex504/Em511 nm for the ER Tracker, Ex380/Em576 nm for the Lyso Tracker, and Ex490/Em516 nm for the Mito Tracker.

    Article Title: FG repeats drive co-clustering of nuclear pores and P granules in the C. elegans germline
    Article Snippet: Animals were imaged using an inverted Zeiss Axio Observer with CSU-W1 SoRa spinning disk scan head (Yokogawa), 1×/2.8×/4× relay lens (Yokogawa) and an iXon Life 888 EMCCD camera (Andor) controlled by Slidebook 6.0 software (Intelligent Imaging Innovations).

    Article Title: The HCF101 protein is an important component of the cytosolic iron-sulfur synthesis pathway in Toxoplasma gondii.
    Article Snippet: Trails length (at least 100 per condition) were captured on random fields with a 63× objective on a Zeiss AXIO Imager Z2 epifluorescence microscope and were quantified using the NeuronJ plug-in on the ImageJ software as described previously [86].

    Article Title: Mice lacking Astn2 have ASD-like behaviors and altered cerebellar circuit properties
    Article Snippet: Slices were imaged using an upright wide-field brightfield Axioplan 2 microscope fitted with a 40× or 63× objective (Zeiss).

    Article Title: The HCF101 protein is an important component of the cytosolic iron–sulfur synthesis pathway in Toxoplasma gondii
    Article Snippet: Trails length (at least 100 per condition) were captured on random fields with a 63× objective on a Zeiss AXIO Imager Z2 epifluorescence microscope and were quantified using the NeuronJ plug-in on the ImageJ software as described previously [ ].

    Article Title: Distinct functional domains of Dystroglycan regulate inhibitory synapse formation and maintenance in cerebellar Purkinje cells
    Article Snippet: For analysis of synaptic colocalization, puncta density, and puncta volume: 0.2 μm z-stacks covering 5μm were acquired using a 63× objective on a Zeiss LSM 980 (as described above) such that the PC layer and molecular layer were captured in the image.

    Confocal Microscopy:

    Article Title: Shielding siRNA by peptide-based nanofibers: An efficient approach for turning off EGFR gene in breast cancer.
    Article Snippet: Cells were treated with NF/EGFR-(FITC)siRNA (25 pmol of siRNA) and incubated for 5 h. After this period of incubation, the cells were fixed by formaldehyde solution 4 % v/v and the nucleus was stained by DAPI (BIOTIUM) while cellular membrane stained with CellBrite Cytoplasmic Membrane dye (BIOTIUM). .. Finally, the cellular uptake of the FITC-siRNA was evaluated by confocal microscopy and fluorescence intensity was monitored to visualize DAPI (Ex/Em = 350/465 nm) as nuclear stain, cellular membranes (Alexa 647, Ex/Em = 650/665 nm) and siRNA conjugated with FITC (Alexa 488, Ex = 490/525 nm), using a confocal microscope (Zeiss LSM 900 Airyscan 2) at 40× magnification (oil immersion objective lens) [35,59]. ..

    Fluorescence:

    Article Title: Shielding siRNA by peptide-based nanofibers: An efficient approach for turning off EGFR gene in breast cancer.
    Article Snippet: Cells were treated with NF/EGFR-(FITC)siRNA (25 pmol of siRNA) and incubated for 5 h. After this period of incubation, the cells were fixed by formaldehyde solution 4 % v/v and the nucleus was stained by DAPI (BIOTIUM) while cellular membrane stained with CellBrite Cytoplasmic Membrane dye (BIOTIUM). .. Finally, the cellular uptake of the FITC-siRNA was evaluated by confocal microscopy and fluorescence intensity was monitored to visualize DAPI (Ex/Em = 350/465 nm) as nuclear stain, cellular membranes (Alexa 647, Ex/Em = 650/665 nm) and siRNA conjugated with FITC (Alexa 488, Ex = 490/525 nm), using a confocal microscope (Zeiss LSM 900 Airyscan 2) at 40× magnification (oil immersion objective lens) [35,59]. ..

    Staining:

    Article Title: Shielding siRNA by peptide-based nanofibers: An efficient approach for turning off EGFR gene in breast cancer.
    Article Snippet: Cells were treated with NF/EGFR-(FITC)siRNA (25 pmol of siRNA) and incubated for 5 h. After this period of incubation, the cells were fixed by formaldehyde solution 4 % v/v and the nucleus was stained by DAPI (BIOTIUM) while cellular membrane stained with CellBrite Cytoplasmic Membrane dye (BIOTIUM). .. Finally, the cellular uptake of the FITC-siRNA was evaluated by confocal microscopy and fluorescence intensity was monitored to visualize DAPI (Ex/Em = 350/465 nm) as nuclear stain, cellular membranes (Alexa 647, Ex/Em = 650/665 nm) and siRNA conjugated with FITC (Alexa 488, Ex = 490/525 nm), using a confocal microscope (Zeiss LSM 900 Airyscan 2) at 40× magnification (oil immersion objective lens) [35,59]. ..

    Microscopy:

    Article Title: Shielding siRNA by peptide-based nanofibers: An efficient approach for turning off EGFR gene in breast cancer.
    Article Snippet: Cells were treated with NF/EGFR-(FITC)siRNA (25 pmol of siRNA) and incubated for 5 h. After this period of incubation, the cells were fixed by formaldehyde solution 4 % v/v and the nucleus was stained by DAPI (BIOTIUM) while cellular membrane stained with CellBrite Cytoplasmic Membrane dye (BIOTIUM). .. Finally, the cellular uptake of the FITC-siRNA was evaluated by confocal microscopy and fluorescence intensity was monitored to visualize DAPI (Ex/Em = 350/465 nm) as nuclear stain, cellular membranes (Alexa 647, Ex/Em = 650/665 nm) and siRNA conjugated with FITC (Alexa 488, Ex = 490/525 nm), using a confocal microscope (Zeiss LSM 900 Airyscan 2) at 40× magnification (oil immersion objective lens) [35,59]. ..



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