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olympus bx51wi microscope  (Olympus)


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    Structured Review

    Olympus olympus bx51wi microscope
    Olympus Bx51wi Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 3230 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/microscope+stage/BX61WI%2FBX51WI+Fixed+Stage+Microscope/pm42893407-436-12-12
    Average 99 stars, based on 3230 article reviews
    olympus bx51wi microscope - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Microscopy:

    Article Title: Phenotype and gene signature of testicular tumors in 129.MOLF‐Chr19 mice resemble human teratomas
    Article Snippet: .. An Axio Scope A1 microscope (Leica, Wetzlar, Germany) was used for direct histopathological evaluation of tissue sections, whereas microphotographs were acquired by scanning the slides with a computer‐directed microscope stage (Olympus SLIDEVIEW VS200, Evident, Hamburg, Germany). ..

    Article Title: Deciphering migraine pain mechanisms through electrophysiological insights of trigeminal ganglion neurons.
    Article Snippet: .. First, the trigeminal ganglion neuron samples were placed in plastic chambers and set on the microscope stage (Olympus BX51WI, Olympus, Japan). ..

    Article Title: Oxylipins produced by Pseudomonas aeruginosa promote biofilm formation and virulence.
    Article Snippet: .. The cover slips were incubated for 6 h at 37 C, then placed inverted on the microscope stage (Olympus BX53 system microscope) and the twitching motility filmed using an XM10 incorporated camera (Olympus) controlled by the software cellSens Standard 1.6 (Olympus). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy.
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Micro- scope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging (Figures 2 and 3). g. Excite Cal-520 indicator using a 488 nm laser (set the intensity to a minimum such that the in- dicator fluorescence does not photobleach; see solution in ‘‘problems 2 and 3’’); ensure that the cells are in focus and in the incident angle of the laser achieves TIRF (Figures 2, 3A, 3C, and 3E). ..

    Article Title: Control of Synaptic Communication through Molecularly Engineered Bioluminescence Light Emission and Sensing
    Article Snippet: .. Recordings were made from co-culture coverslips attached to the bottom of a recording chamber (RC26-GLP, Warner Instruments) fixed to a microscope stage (BX51WI, Olympus). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Microscope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging ( and ). ..

    Article Title: [1909.03992] Acoustomicrofluidic separation of tardigrades from raw cultures for sample preparation
    Article Snippet: After repeated passive filtration, the processed sample was loaded into a separate syringe and injected into the active microfluidic tardigrade separation device using a syringe pump (neMESYS, CETONI GmbH) along with two sheath flows (pure DI water). .. The SAWbased active separation device was mounted on top of a microscope stage (BX53, Olympus), and a 10-bit high-speed COMS camera (pco.1200 hs, PCO) was used to capture the images. .. An RF signal generator (N5181A, Agilent Technologies) and an amplifier (LZT-22+, Mini-Circuits) were used to produce high-frequency (45 MHz and 72 MHz) AC signals with varying amplitude to actuate the IDTs.

    Incubation:

    Article Title: Oxylipins produced by Pseudomonas aeruginosa promote biofilm formation and virulence.
    Article Snippet: .. The cover slips were incubated for 6 h at 37 C, then placed inverted on the microscope stage (Olympus BX53 system microscope) and the twitching motility filmed using an XM10 incorporated camera (Olympus) controlled by the software cellSens Standard 1.6 (Olympus). ..

    Software:

    Article Title: Oxylipins produced by Pseudomonas aeruginosa promote biofilm formation and virulence.
    Article Snippet: .. The cover slips were incubated for 6 h at 37 C, then placed inverted on the microscope stage (Olympus BX53 system microscope) and the twitching motility filmed using an XM10 incorporated camera (Olympus) controlled by the software cellSens Standard 1.6 (Olympus). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy.
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Micro- scope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging (Figures 2 and 3). g. Excite Cal-520 indicator using a 488 nm laser (set the intensity to a minimum such that the in- dicator fluorescence does not photobleach; see solution in ‘‘problems 2 and 3’’); ensure that the cells are in focus and in the incident angle of the laser achieves TIRF (Figures 2, 3A, 3C, and 3E). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Microscope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging ( and ). ..

    Imaging:

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy.
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Micro- scope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging (Figures 2 and 3). g. Excite Cal-520 indicator using a 488 nm laser (set the intensity to a minimum such that the in- dicator fluorescence does not photobleach; see solution in ‘‘problems 2 and 3’’); ensure that the cells are in focus and in the incident angle of the laser achieves TIRF (Figures 2, 3A, 3C, and 3E). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Microscope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging ( and ). ..

    Inverted Microscopy:

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy.
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Micro- scope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging (Figures 2 and 3). g. Excite Cal-520 indicator using a 488 nm laser (set the intensity to a minimum such that the in- dicator fluorescence does not photobleach; see solution in ‘‘problems 2 and 3’’); ensure that the cells are in focus and in the incident angle of the laser achieves TIRF (Figures 2, 3A, 3C, and 3E). ..

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Microscope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging ( and ). ..

    Article Title: Method of treating metastatic cancer
    Article Snippet: .. Peptide was added to treated wells at 15 uM at 12 hour intervals and images were taken with a MoticTM camera on an Olympus inverted-microscope stage. .. Peptide was added to treated wells at 15 uM at 12 hour intervals and images were taken with a Motic camera on an Olympus inverted-microscope stage.

    Fluorescence:

    Article Title: A protocol for detecting elemental calcium signals (Ca 2+ puffs) in mammalian cells using total internal reflection fluorescence microscopy.
    Article Snippet: .. Add 1 mL imaging buffer to the perfusion chamber to ensure that the cells are properly immersed. c. Clean the bottom of the cover slip using a kimwipe to avoid artifacts while focusing/imaging. d. On an Olympus IX81 inverted microscope equipped with PlanApo 60x/1.45 Oil TIRFM Micro- scope Objective, place a drop of low autofluorescence immersion oil. e. Next, fasten the Warner perfusion chamber on to the microscope stage. f. We use Olympus CellSens Dimensions 2.3 (Build 189987) software for imaging (Figures 2 and 3). g. Excite Cal-520 indicator using a 488 nm laser (set the intensity to a minimum such that the in- dicator fluorescence does not photobleach; see solution in ‘‘problems 2 and 3’’); ensure that the cells are in focus and in the incident angle of the laser achieves TIRF (Figures 2, 3A, 3C, and 3E). ..



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    Image Search Results


    Journal: iScience

    Article Title: Sleep deprivation impairs ventral hippocampus-medial prefrontal connectivity and task learning in rats

    doi: 10.1016/j.isci.2026.115683

    Figure Lengend Snippet:

    Article Snippet: Optical microscope , Olympus , BX51WI.

    Techniques: Recombinant, Software, Functional Assay, Imaging, Microscopy

    Journal: iScience

    Article Title: A Ca²⁺ level-independent component of recovery from sensory adaptation supports continuous vesicle supply at cochlear hair cell ribbon synapses

    doi: 10.1016/j.isci.2026.117694

    Figure Lengend Snippet:

    Article Snippet: Excised apical turns of 9–11 days-old rat cochleae (Sprague-Dawley, either sex) were placed into a chamber under an upright microscope (Olympus, BX51WI) and superfused with extracellular solution at 2–3 mL/minute.

    Techniques: Recombinant, Software, Microscopy, Glass, Transferring