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inverted epifluorescence microscope te2000- e- pfs  (Nikon)


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    Structured Review

    Nikon inverted epifluorescence microscope te2000- e- pfs
    Inverted Epifluorescence Microscope Te2000 E Pfs, 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/inverted+microscope+te2000-pfs/pm39869799-450-10-18
    Average 90 stars, based on 1 article reviews
    inverted epifluorescence microscope te2000- e- pfs - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    Imaging:

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equipped with a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: Cell culture container and method of producing the same
    Article Snippet: The degrees of cell network formation were observed using an inverted microscope (TE2000-PFS) produced by Nikon Corporation.

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration.
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equippedwith a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: N-terminal β-strand of single-headed kinesin-1 can modulate the off-axis force-generation and resultant rotation pitch.
    Article Snippet: Funding information JSPS KAKENHI, Grant/Award Numbers: JP19H03190, JP19H05357, JP19H05378, JP20K06635, JP20K15744, JPJSBP12

    Article Title: Switching direction in electric-signal-induced cell migration by cyclic guanosine monophosphate and phosphatidylinositol signaling
    Article Snippet: To visualize GFP fused proteins, cells were examined through an inverted microscope (TE2000-PFS; Nikon) with an Apo TIRF 60×1.49 oil immersion lens.

    Article Title: DNA damage strength modulates a bimodal switch of p53 dynamics for cell-fate control
    Article Snippet: Cell images were acquired with an inverted microscope (TE2000-PFS; Nikon, Tokyo, Japan) enclosed in a humidified chamber maintained at 37°C.

    Inverted Microscopy:

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equipped with a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: Cell culture container and method of producing the same
    Article Snippet: The degrees of cell network formation were observed using an inverted microscope (TE2000-PFS) produced by Nikon Corporation.

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration.
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equippedwith a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: N-terminal β-strand of single-headed kinesin-1 can modulate the off-axis force-generation and resultant rotation pitch.
    Article Snippet: Funding information JSPS KAKENHI, Grant/Award Numbers: JP19H03190, JP19H05357, JP19H05378, JP20K06635, JP20K15744, JPJSBP12

    Article Title: Switching direction in electric-signal-induced cell migration by cyclic guanosine monophosphate and phosphatidylinositol signaling
    Article Snippet: To visualize GFP fused proteins, cells were examined through an inverted microscope (TE2000-PFS; Nikon) with an Apo TIRF 60×1.49 oil immersion lens.

    Article Title: DNA damage strength modulates a bimodal switch of p53 dynamics for cell-fate control
    Article Snippet: Cell images were acquired with an inverted microscope (TE2000-PFS; Nikon, Tokyo, Japan) enclosed in a humidified chamber maintained at 37°C.

    Fluorescence:

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equipped with a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: Cell culture container and method of producing the same
    Article Snippet: The degrees of cell network formation were observed using an inverted microscope (TE2000-PFS) produced by Nikon Corporation.

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration.
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equippedwith a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: N-terminal β-strand of single-headed kinesin-1 can modulate the off-axis force-generation and resultant rotation pitch.
    Article Snippet: Funding information JSPS KAKENHI, Grant/Award Numbers: JP19H03190, JP19H05357, JP19H05378, JP20K06635, JP20K15744, JPJSBP12

    Article Title: Switching direction in electric-signal-induced cell migration by cyclic guanosine monophosphate and phosphatidylinositol signaling
    Article Snippet: To visualize GFP fused proteins, cells were examined through an inverted microscope (TE2000-PFS; Nikon) with an Apo TIRF 60×1.49 oil immersion lens.

    Article Title: DNA damage strength modulates a bimodal switch of p53 dynamics for cell-fate control
    Article Snippet: Cell images were acquired with an inverted microscope (TE2000-PFS; Nikon, Tokyo, Japan) enclosed in a humidified chamber maintained at 37°C.

    Produced:

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equipped with a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: Cell culture container and method of producing the same
    Article Snippet: The degrees of cell network formation were observed using an inverted microscope (TE2000-PFS) produced by Nikon Corporation.

    Article Title: Self-organization of the phosphatidylinositol lipids signaling system for random cell migration.
    Article Snippet: Fluorescence images were obtained by using an inverted microscope (TE2000-PFS; Nikon) equippedwith a confocal unit (CSU-10; Yokogawa) through a 60× oil immersion objective lens (N.A.

    Article Title: N-terminal β-strand of single-headed kinesin-1 can modulate the off-axis force-generation and resultant rotation pitch.
    Article Snippet: Funding information JSPS KAKENHI, Grant/Award Numbers: JP19H03190, JP19H05357, JP19H05378, JP20K06635, JP20K15744, JPJSBP12

    Article Title: Switching direction in electric-signal-induced cell migration by cyclic guanosine monophosphate and phosphatidylinositol signaling
    Article Snippet: To visualize GFP fused proteins, cells were examined through an inverted microscope (TE2000-PFS; Nikon) with an Apo TIRF 60×1.49 oil immersion lens.

    Article Title: DNA damage strength modulates a bimodal switch of p53 dynamics for cell-fate control
    Article Snippet: Cell images were acquired with an inverted microscope (TE2000-PFS; Nikon, Tokyo, Japan) enclosed in a humidified chamber maintained at 37°C.



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