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4 well dish  (Greiner Bio)


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    Structured Review

    Greiner Bio 4 well dish
    4 Well Dish, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 96/100, based on 732 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cellview+cell+culture+dish+627860/Cellview+Cell+Culture+Dish+Ps+35%2F10+Mm/pm41915835-413-6-8
    Average 96 stars, based on 732 article reviews
    4 well dish - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Injection:

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease.
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Imaging:

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease.
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Article Title: β-tubulin phosphorylation by Chk1 is required for normal spindle formation during cell division.
    Article Snippet: .. Time-lapse imaging and Biotracker staining HEK 293T cells were seeded onto 35-mm diameter Petri dishes with a 175 μm-thickness glass base (Greiner, #627860) and an inverted fluorescence microscope (Observer D1; Zeiss) was used. ..

    Laser-Scanning Microscopy:

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease.
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Article Title: A zebrafish multimodal toolbox to study the blood-brain barrier in health and disease
    Article Snippet: .. Injected Tg(fli1:EGFP) and non-injected Tg(cldn5a: EGFP) zebrafish larvae were anesthetized with tricaine and mounted in 0.8% LMP agarose on a glass bottom imaging dish (Cat. No. 627860; Greiner bio-one) with their yolk sac facing upwards and were imaged within 3 h. Image analysis was performed with a confocal laser scanning microscope (Leica TCS SP8 X/ Leica TCS SP8 SMD/Leica Stellaris 8; Leica DMI 6000) using a 20x dry objective (NA 0.75) and 40x oil immersion objective (NA 1.30). ..

    Confocal Microscopy:

    Article Title: Optogenetic mediated contractility enables reversible control of microglial morphology and migration in vivo.
    Article Snippet: Embryos were embedded in 1–1.3% low-melting (LM) agarose (PeqGOLD Low Melt Agarose, PeqLab Biotechnologie GmbH), dissolved in E3 medium with 0.01% tricaine. .. Embryos were mounted on glass-bottom dishes (Greiner Bio-One, #627871) for confocal microscopy or pulled together with agar into glass capillaries (Brand, #701904) with a rod (Brand, #701932), and then pushed halfway out, into the microscopy chamber for light–sheet microscopy on the Zeiss Z.1. .. For light-sheet microscopy on the Leica Viventis LS2 Live, each zebrafish embryo was mounted head down in one well of a 3 well sample chamber (Viventis, custom made) filled with E3 containing 0.01% tricaine and 0.003% PTU.

    Microscopy:

    Article Title: Optogenetic mediated contractility enables reversible control of microglial morphology and migration in vivo.
    Article Snippet: Embryos were embedded in 1–1.3% low-melting (LM) agarose (PeqGOLD Low Melt Agarose, PeqLab Biotechnologie GmbH), dissolved in E3 medium with 0.01% tricaine. .. Embryos were mounted on glass-bottom dishes (Greiner Bio-One, #627871) for confocal microscopy or pulled together with agar into glass capillaries (Brand, #701904) with a rod (Brand, #701932), and then pushed halfway out, into the microscopy chamber for light–sheet microscopy on the Zeiss Z.1. .. For light-sheet microscopy on the Leica Viventis LS2 Live, each zebrafish embryo was mounted head down in one well of a 3 well sample chamber (Viventis, custom made) filled with E3 containing 0.01% tricaine and 0.003% PTU.

    Article Title: β-tubulin phosphorylation by Chk1 is required for normal spindle formation during cell division.
    Article Snippet: .. Time-lapse imaging and Biotracker staining HEK 293T cells were seeded onto 35-mm diameter Petri dishes with a 175 μm-thickness glass base (Greiner, #627860) and an inverted fluorescence microscope (Observer D1; Zeiss) was used. ..

    Expressing:

    Article Title: Endoplasmic Reticulum Geometry Dictates Neuronal Bursting via Calcium Store Refill Rates and Exposes Selective Neuronal Vulnerability.
    Article Snippet: .. Cells were then seeded n a 4-well dish (Greiner Bio-One, 627975) and expression of he Ca2 + sensors was induced by adding Dox (1 μg/mL) for 3 ays. .. Cells were imaged on a STELARIS8 confocal microscope Leica, Wetzlar, Germany) with a controlled environment (37◦C, % CO2 ).

    Staining:

    Article Title: β-tubulin phosphorylation by Chk1 is required for normal spindle formation during cell division.
    Article Snippet: .. Time-lapse imaging and Biotracker staining HEK 293T cells were seeded onto 35-mm diameter Petri dishes with a 175 μm-thickness glass base (Greiner, #627860) and an inverted fluorescence microscope (Observer D1; Zeiss) was used. ..

    Fluorescence:

    Article Title: β-tubulin phosphorylation by Chk1 is required for normal spindle formation during cell division.
    Article Snippet: .. Time-lapse imaging and Biotracker staining HEK 293T cells were seeded onto 35-mm diameter Petri dishes with a 175 μm-thickness glass base (Greiner, #627860) and an inverted fluorescence microscope (Observer D1; Zeiss) was used. ..



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