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microscope nikon eclipse 90i epifluorescence microscope  (Nikon)


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    Structured Review

    Nikon microscope nikon eclipse 90i epifluorescence microscope
    Microscope Nikon Eclipse 90i Epifluorescence Microscope, supplied by Nikon, 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/90i+eclipse+epifluorescence+microscope/pm40346605-324-8-9
    Average 90 stars, based on 1 article reviews
    microscope nikon eclipse 90i epifluorescence microscope - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Cell type-specific role of CBX2 and its disordered region in spermatogenesis
    Article Snippet: Coverslips were put on top of sections with mounting media (VectaShield, Vector Laboratories H-1000) and sealed with nail polish (Fisher Scientific 72180). .. Slides were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an ORCA-ER-1394 CCD camera (Hamamatsu). ..

    Article Title: Elongin A associates with actively transcribed genes and modulates enhancer RNA levels with limited impact on transcription elongation rate in vivo
    Article Snippet: .. Images were acquired using the 100× oil objective on Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera and velocity imaging software (Perkin Elmer). ..

    Article Title: Cell type-specific role of CBX2 and its disordered region in spermatogenesis.
    Article Snippet: Coverslips were put on top of sections with mounting media (VectaShield, Vector Laboratories H-1000) and sealed with nail polish (Fisher Scientific 72180). .. Slides were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an ORCA-ER-1394 CCD camera (Hamamatsu). ..

    Article Title: A Polycomb domain found in committed cells impairs differentiation when introduced into PRC1 in pluripotent cells.
    Article Snippet: Coverslips were mounted on slides with Vectashield mounting media containing DAPI (Vector Laboratories). .. Cells were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (PerkinElmer). ..

    Article Title: Phase separation and nucleosome compaction are governed by the same domain of Polycomb Repressive Complex 1
    Article Snippet: .. Proteins were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (Perkin Elmer). ..

    Article Title: Phase separation of Polycomb-repressive complex 1 is governed by a charged disordered region of CBX2
    Article Snippet: .. Proteins were imaged at room temperature with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100× oil objective and Volocity software (Perkin Elmer). ..

    Article Title: A Polycomb domain found in committed cells impairs differentiation when introduced into PRC1 in pluripotent cells.
    Article Snippet: .. The proteins were loaded onto glass slides with coverslips and imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (Perkin Elmer). ..

    Imaging:

    Article Title: Elongin A associates with actively transcribed genes and modulates enhancer RNA levels with limited impact on transcription elongation rate in vivo
    Article Snippet: .. Images were acquired using the 100× oil objective on Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera and velocity imaging software (Perkin Elmer). ..

    Software:

    Article Title: Elongin A associates with actively transcribed genes and modulates enhancer RNA levels with limited impact on transcription elongation rate in vivo
    Article Snippet: .. Images were acquired using the 100× oil objective on Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera and velocity imaging software (Perkin Elmer). ..

    Article Title: A Polycomb domain found in committed cells impairs differentiation when introduced into PRC1 in pluripotent cells.
    Article Snippet: Coverslips were mounted on slides with Vectashield mounting media containing DAPI (Vector Laboratories). .. Cells were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (PerkinElmer). ..

    Article Title: Phase separation and nucleosome compaction are governed by the same domain of Polycomb Repressive Complex 1
    Article Snippet: .. Proteins were imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (Perkin Elmer). ..

    Article Title: Phase separation of Polycomb-repressive complex 1 is governed by a charged disordered region of CBX2
    Article Snippet: .. Proteins were imaged at room temperature with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100× oil objective and Volocity software (Perkin Elmer). ..

    Article Title: A Polycomb domain found in committed cells impairs differentiation when introduced into PRC1 in pluripotent cells.
    Article Snippet: .. The proteins were loaded onto glass slides with coverslips and imaged with a Nikon 90i Eclipse epifluorescence microscope equipped with an Orca ER camera (Hamamatsu) using a 100X oil objective and Volocity software (Perkin Elmer). ..



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    Adult salivary gland cellular architecture of the cat flea ( C. felis ). (A) Fluorescent staining of female salivary glands dissected 3-days post-feeding. The tissues were fixed with Bouin's solution and permeabilized using 0.1 % Triton X-100 in PBS. Nuclei were labeled with DAPI (blue signal in merged images), and salivary glands were counterstained with Evans blue (red fluorescent signal in merged images). Scale bar represents 100 μm (upper row) and 50 μm (lower row); (B) Fluorescent staining of female salivary glands dissected 7-days post-feeding. The samples were fixed with 4 % paraformaldehyde in cytoskeleton-stabilizing PHEM buffer and permeabilized using 0.1 % Triton X-100 in PBS. Actin filaments were labeled with conjugated phalloidin (purple signal), and nuclei were stained with DAPI (blue signal). Salivary glands were treated with a Vector TrueVIEW autofluorescence quenching kit. Scale bar represents 100 μm; (C) Comparative images of female salivary glands 1- and 14-days post-feeding (dpf), and differences in salivary gland structure between sexes. The preparations were fixed with Bouin's solution and permeabilized with 0.1 % Triton X-100 in PBS. Gland and duct nuclei were visualized with DAPI (blue signal). Scale bar represents 100 μm. The terminology of the flea's internal anatomy is according to . Abbreviations: BF, bright-field microscopy; CD, striated cuticle of duct; EC, epithelial (secretory) cell; L, lumen; N, nucleus; SD, salivary duct; SG, salivary glands. Micrographs on panel A were taken using a Nikon Eclipse <t>90i</t> <t>microscope,</t> and images on panels B and C were captured using an LSM 980 Airy Scan II confocal microscope. Created with BioRender.com .
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    Nikon epifluorescence microscope nikon eclipse 90i
    Adult salivary gland cellular architecture of the cat flea ( C. felis ). (A) Fluorescent staining of female salivary glands dissected 3-days post-feeding. The tissues were fixed with Bouin's solution and permeabilized using 0.1 % Triton X-100 in PBS. Nuclei were labeled with DAPI (blue signal in merged images), and salivary glands were counterstained with Evans blue (red fluorescent signal in merged images). Scale bar represents 100 μm (upper row) and 50 μm (lower row); (B) Fluorescent staining of female salivary glands dissected 7-days post-feeding. The samples were fixed with 4 % paraformaldehyde in cytoskeleton-stabilizing PHEM buffer and permeabilized using 0.1 % Triton X-100 in PBS. Actin filaments were labeled with conjugated phalloidin (purple signal), and nuclei were stained with DAPI (blue signal). Salivary glands were treated with a Vector TrueVIEW autofluorescence quenching kit. Scale bar represents 100 μm; (C) Comparative images of female salivary glands 1- and 14-days post-feeding (dpf), and differences in salivary gland structure between sexes. The preparations were fixed with Bouin's solution and permeabilized with 0.1 % Triton X-100 in PBS. Gland and duct nuclei were visualized with DAPI (blue signal). Scale bar represents 100 μm. The terminology of the flea's internal anatomy is according to . Abbreviations: BF, bright-field microscopy; CD, striated cuticle of duct; EC, epithelial (secretory) cell; L, lumen; N, nucleus; SD, salivary duct; SG, salivary glands. Micrographs on panel A were taken using a Nikon Eclipse <t>90i</t> <t>microscope,</t> and images on panels B and C were captured using an LSM 980 Airy Scan II confocal microscope. Created with BioRender.com .
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    https://www.bioz.com/product/90i+eclipse+epifluorescence+microscope/bio_rxiv__2024__02__01__578426-211-46-48
    Average 90 stars, based on 1 article reviews
    epifluorescence microscope nikon eclipse 90i - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    Adult salivary gland cellular architecture of the cat flea ( C. felis ). (A) Fluorescent staining of female salivary glands dissected 3-days post-feeding. The tissues were fixed with Bouin's solution and permeabilized using 0.1 % Triton X-100 in PBS. Nuclei were labeled with DAPI (blue signal in merged images), and salivary glands were counterstained with Evans blue (red fluorescent signal in merged images). Scale bar represents 100 μm (upper row) and 50 μm (lower row); (B) Fluorescent staining of female salivary glands dissected 7-days post-feeding. The samples were fixed with 4 % paraformaldehyde in cytoskeleton-stabilizing PHEM buffer and permeabilized using 0.1 % Triton X-100 in PBS. Actin filaments were labeled with conjugated phalloidin (purple signal), and nuclei were stained with DAPI (blue signal). Salivary glands were treated with a Vector TrueVIEW autofluorescence quenching kit. Scale bar represents 100 μm; (C) Comparative images of female salivary glands 1- and 14-days post-feeding (dpf), and differences in salivary gland structure between sexes. The preparations were fixed with Bouin's solution and permeabilized with 0.1 % Triton X-100 in PBS. Gland and duct nuclei were visualized with DAPI (blue signal). Scale bar represents 100 μm. The terminology of the flea's internal anatomy is according to . Abbreviations: BF, bright-field microscopy; CD, striated cuticle of duct; EC, epithelial (secretory) cell; L, lumen; N, nucleus; SD, salivary duct; SG, salivary glands. Micrographs on panel A were taken using a Nikon Eclipse 90i microscope, and images on panels B and C were captured using an LSM 980 Airy Scan II confocal microscope. Created with BioRender.com .

    Journal: Current Research in Insect Science

    Article Title: Salivary glands of the cat flea, Ctenocephalides felis : Dissection and microscopy guide

    doi: 10.1016/j.cris.2024.100080

    Figure Lengend Snippet: Adult salivary gland cellular architecture of the cat flea ( C. felis ). (A) Fluorescent staining of female salivary glands dissected 3-days post-feeding. The tissues were fixed with Bouin's solution and permeabilized using 0.1 % Triton X-100 in PBS. Nuclei were labeled with DAPI (blue signal in merged images), and salivary glands were counterstained with Evans blue (red fluorescent signal in merged images). Scale bar represents 100 μm (upper row) and 50 μm (lower row); (B) Fluorescent staining of female salivary glands dissected 7-days post-feeding. The samples were fixed with 4 % paraformaldehyde in cytoskeleton-stabilizing PHEM buffer and permeabilized using 0.1 % Triton X-100 in PBS. Actin filaments were labeled with conjugated phalloidin (purple signal), and nuclei were stained with DAPI (blue signal). Salivary glands were treated with a Vector TrueVIEW autofluorescence quenching kit. Scale bar represents 100 μm; (C) Comparative images of female salivary glands 1- and 14-days post-feeding (dpf), and differences in salivary gland structure between sexes. The preparations were fixed with Bouin's solution and permeabilized with 0.1 % Triton X-100 in PBS. Gland and duct nuclei were visualized with DAPI (blue signal). Scale bar represents 100 μm. The terminology of the flea's internal anatomy is according to . Abbreviations: BF, bright-field microscopy; CD, striated cuticle of duct; EC, epithelial (secretory) cell; L, lumen; N, nucleus; SD, salivary duct; SG, salivary glands. Micrographs on panel A were taken using a Nikon Eclipse 90i microscope, and images on panels B and C were captured using an LSM 980 Airy Scan II confocal microscope. Created with BioRender.com .

    Article Snippet: The preparations were observed using a Zeiss LSM 980 Airy Scan II confocal microscope or Nikon Eclipse 90i epifluorescent microscope.

    Techniques: Staining, Labeling, Plasmid Preparation, Microscopy