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inverted microscope nikon eclipse te-2000u  (Nikon)


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    Nikon inverted microscope nikon eclipse te-2000u
    Inverted Microscope Nikon Eclipse Te 2000u, 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+eclipse+te-2000u/pmc12226173-77-12-13
    Average 90 stars, based on 1 article reviews
    inverted microscope nikon eclipse te-2000u - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: TASK-1 induces gefitinib resistance by promoting cancer initiating cell formation and epithelial-mesenchymal transition in lung cancer
    Article Snippet: Images of the wounded areas were captured at different time-points with an inverted microscope (Eclipse TE-2000U; Nikon, Tokyo, Japan) equipped with a video camera (DS-U1; Nikon).

    Article Title: Interaction of propofol with voltage-gated human Kv1.5 channel through specific amino acids within the pore region.
    Article Snippet: The intravenous anesthetic propofol affects the function of a diversity of ligand-gated and voltage-gated ion channels.. However, there is little information as to whether propofol directly interacts with voltage-gated ion channel proteins to modulate their functions.. The Kv1.5 channel is activated by membrane depolarization during action potentials and contributes to atrial repolarization in the human heart.

    Article Title: TASK-1 induces gefitinib resistance by promoting cancer initiating cell formation and epithelial-mesenchymal transition in lung cancer.
    Article Snippet: Images of the wounded areas were captured at different time-points with an inverted microscope (Eclipse TE‐2000U; Nikon, Tokyo, Japan) equipped with a video camera (DS‐U1; Nikon).

    Article Title: Serum albumin attenuates the open-channel blocking effects of propofol on the human Kv1.5 channel.
    Article Snippet: The intravenous anesthetic propofol modulates various ion channel functions.. It is generally accepted that approximately 98% of propofol binds to blood constituents and that the free (unbound) drug preferentially affects target proteins including ion channels.. However, modulatory effects of propofol on ion channels have not been previously explored in the presence of serum albumin.

    Article Title: Clinical and neonatal outcomes of complete zona pellucida removal by laser-assisted hatching after single vitrified-warmed blastocyst transfer.
    Article Snippet: Laser-assisted hatching (LAH) is a widely used and unavoidable technique in assisted reproductive technology after frozen embryo transfer (FET).. We aimed to investigate the safety and efficacy of completely ZP (zona pellucida) removed by an assisted laser group compared to an intact group after FET.. This retrospective study involved 320 SVBT single vitrifiedwarmed blastocyst transfers of 213 patients who underwent clomiphene citrate (CC) based minimal stimulation protocol.

    Inverted Microscopy:

    Article Title: The miR-370 /UQCRC2 axis facilitates tumorigenesis by regulating epithelial-mesenchymal transition in Gastric Cancer
    Article Snippet: .. A Nikon inverted microscope (ECLIPSE TE-2000U), equipped with a video camera (DS-U1, Nikon), was used to capture images 0 and 24 h after wounding. .. A transwell insert pre-coated with Matrigel (Corning, Inc., Corning, NY, USA) was used to test the invasiveness of GC cells.

    Article Title: Activation of ARK5/miR-1181/HOXA10 axis promotes epithelial-mesenchymal transition in ovarian cancer.
    Article Snippet: .. The wounded areas were photographed at the beginning (0 h, top panels) and the end (10 h, bottom panels) of the assay using a Nikon inverted microscope (Eclipse TE-2000U) equipped with a video camera (DS-U1) (both from Nikon, Japan). ..



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    Image Search Results


    TIRFM configuration to study HCs transport to appositional and non-appositional plasma membrane zones. A representative cartoon showing two cells in juxtaposition and all the components involved in the data acquisition. TIRF microscopy configuration utilizes a critical angle, which creates a 100–200 nm-deep evanescent wave between the glass coverslip surface and cells to excite fluorophores located in the vicinity of the plasma membrane. Analysis was performed in the appositional and non-appositional zones ( a ). An example of how TIFR configuration is achieved under the microscopy is shown ( b ). Tagged connexins were illuminated in epifluorescence (left panel). Then, the surface reflective interference contrast (SRIC) filter ensures an appropriate field with cells attached to the glass (middle panel). Finally, it is switched to TIRF microscopy configuration for the data acquisition (right panel) ( b ).

    Journal: International Journal of Molecular Sciences

    Article Title: Differential Regulation of Hemichannels and Gap Junction Channels by RhoA GTPase and Actin Cytoskeleton: A Comparative Analysis of Cx43 and Cx26

    doi: 10.3390/ijms25137246

    Figure Lengend Snippet: TIRFM configuration to study HCs transport to appositional and non-appositional plasma membrane zones. A representative cartoon showing two cells in juxtaposition and all the components involved in the data acquisition. TIRF microscopy configuration utilizes a critical angle, which creates a 100–200 nm-deep evanescent wave between the glass coverslip surface and cells to excite fluorophores located in the vicinity of the plasma membrane. Analysis was performed in the appositional and non-appositional zones ( a ). An example of how TIFR configuration is achieved under the microscopy is shown ( b ). Tagged connexins were illuminated in epifluorescence (left panel). Then, the surface reflective interference contrast (SRIC) filter ensures an appropriate field with cells attached to the glass (middle panel). Finally, it is switched to TIRF microscopy configuration for the data acquisition (right panel) ( b ).

    Article Snippet: Images were acquired using a Nikon Eclipse TE-2000U epifluorescence inverted microscope.

    Techniques: Clinical Proteomics, Membrane, Microscopy