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bright field phase contrast microscope nikon-eclipse te 2000-s  (Nikon)


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    Nikon bright field phase contrast microscope nikon-eclipse te 2000-s
    Bright Field Phase Contrast Microscope Nikon Eclipse Te 2000 S, 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/bright+field+phase+contrast+microscope+nikon-eclipse+te+2000-s/pmc11438155-173-15-20
    Average 90 stars, based on 1 article reviews
    bright field phase contrast microscope nikon-eclipse te 2000-s - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: 6 α-Hydroxy-4[14], 10[15]-guainadien-8β, 12-olide induced cell cycle arrest via modulation of EMT and Wnt/β-catenin pathway in HER-2 positive breast cancer cells.
    Article Snippet: Cyathocline purpurea has potential biological activities and has been widely used in traditional Chinese and Ayurvedic medicine.. The aim of the present study is to elucidate the anticancer effect of its 6 α-hydroxy-4[14], 10[15]-guainadien-8β, 12-olide (SRCP1) against HER-2 positive subtype of breast carcinoma.. Anticancer effect of SRCP1 was assessed by cell viability, senescence, apoptosis, cell cycle, DNA synthesis, and gene expression assays.

    Microscopy:

    Article Title: Characterization and angiogenic potential of CD146 + endometrial stem cells
    Article Snippet: .. Formation of endothelial rings was observed at different time points and qualitatively analysed using a bright field phase contrast microscope (Nikon-Eclipse TE 2000-S) and photographed. .. Differentiated endothelial cells were extracted from the matrigel and RNA isolated using the Qiagen RNeasy Mini Kit (Qiagen, Cat. No. 74104) according to the manufacturer’s instructions.

    Article Title: Cancer stem-like cells from head and neck cancers are chemosensitized by the Wnt antagonist, sFRP4, by inducing apoptosis, decreasing stemness, drug resistance and epithelial to mesenchymal transition.
    Article Snippet: .. The secondary spheres were observed for morphology and the total number of spheres were counted, together with the number of spheres of different sizes using a bright field phase contrast microscope (Nikon—Eclipse TE 2000-S) and photographs were taken using a Qimaging—QICAM-fast 1394 (Surrey, BC, Canada). .. Caspase assay After treatment of Hep2 and KB spheroids with the various drug treatments, the activity of apoptosis-inducing caspase-3 was assayed using the EnzChek DEVD-CHO Caspase3 Assay Kit (Invitrogen, Carlsbad, CA, USA), which provides a fluorescent substrate R110.



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    bright field phase contrast microscope nikon-eclipse te 2000-s  (Nikon)
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    Nikon bright field phase contrast microscope nikon-eclipse te 2000-s
    Bright Field Phase Contrast Microscope Nikon Eclipse Te 2000 S, 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/bright+field+phase+contrast+microscope+nikon-eclipse+te+2000-s/pmc11438155-173-15-20
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    Effect of ALV-J on ESCs. (A and B) The morphology of ESCs infected (cESC-ALV-J) or uninfected ( cESC ) with ALV-J under an phase-contrast <t>microscope</t> at 20X (A) and 40X (B). (C) Cell proliferation and cell number calculation. (D) RNA concentration of exosomes from ESCs infected or uninfected with ALV-J. *, P < 0.05. **, P < 0.01. ***, P < 0.001. The scale bar indicates 250 μm. (E) Western blot analysis on cESC-ALV-J and cESC. Results use antibodies against skeletal muscle-specific markers (MYHC and Pax7) and cESC markers (Oct4 and Nanog).
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    Effect of ALV-J on ESCs. (A and B) The morphology of ESCs infected (cESC-ALV-J) or uninfected ( cESC ) with ALV-J under an phase-contrast <t>microscope</t> at 20X (A) and 40X (B). (C) Cell proliferation and cell number calculation. (D) RNA concentration of exosomes from ESCs infected or uninfected with ALV-J. *, P < 0.05. **, P < 0.01. ***, P < 0.001. The scale bar indicates 250 μm. (E) Western blot analysis on cESC-ALV-J and cESC. Results use antibodies against skeletal muscle-specific markers (MYHC and Pax7) and cESC markers (Oct4 and Nanog).
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    bright field phase-contrast microscope nikon-eclipse te 2000-s  (Nikon)
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    Effect of ALV-J on ESCs. (A and B) The morphology of ESCs infected (cESC-ALV-J) or uninfected ( cESC ) with ALV-J under an phase-contrast <t>microscope</t> at 20X (A) and 40X (B). (C) Cell proliferation and cell number calculation. (D) RNA concentration of exosomes from ESCs infected or uninfected with ALV-J. *, P < 0.05. **, P < 0.01. ***, P < 0.001. The scale bar indicates 250 μm. (E) Western blot analysis on cESC-ALV-J and cESC. Results use antibodies against skeletal muscle-specific markers (MYHC and Pax7) and cESC markers (Oct4 and Nanog).
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    Effect of ALV-J on ESCs. (A and B) The morphology of ESCs infected (cESC-ALV-J) or uninfected ( cESC ) with ALV-J under an phase-contrast microscope at 20X (A) and 40X (B). (C) Cell proliferation and cell number calculation. (D) RNA concentration of exosomes from ESCs infected or uninfected with ALV-J. *, P < 0.05. **, P < 0.01. ***, P < 0.001. The scale bar indicates 250 μm. (E) Western blot analysis on cESC-ALV-J and cESC. Results use antibodies against skeletal muscle-specific markers (MYHC and Pax7) and cESC markers (Oct4 and Nanog).

    Journal: Poultry Science

    Article Title: Exosomal circ_CCDC7/gga-miR-6568-3p/Pax7 axis accelerates the differentiation of chicken embryonic stem cells infected with subgroup J avian leukosis virus

    doi: 10.1016/j.psj.2024.103898

    Figure Lengend Snippet: Effect of ALV-J on ESCs. (A and B) The morphology of ESCs infected (cESC-ALV-J) or uninfected ( cESC ) with ALV-J under an phase-contrast microscope at 20X (A) and 40X (B). (C) Cell proliferation and cell number calculation. (D) RNA concentration of exosomes from ESCs infected or uninfected with ALV-J. *, P < 0.05. **, P < 0.01. ***, P < 0.001. The scale bar indicates 250 μm. (E) Western blot analysis on cESC-ALV-J and cESC. Results use antibodies against skeletal muscle-specific markers (MYHC and Pax7) and cESC markers (Oct4 and Nanog).

    Article Snippet: Subsequently, the filter paper was picked up with forceps, and the cESCs in the embryonic disc adsorbed on the filter paper were rinsed into the PBS in the 1.5 mL eppendorf tube. cESCs in PBS were centrifuged at 1,000 rpm for 5 min, resuspended in Dulbecco's Modified Eagle Medium ( DMEM ), seeded at a density of 1 × 10 5 cells in a 6-well plate, and cultured at 39°C with 5% CO 2 for 72 h. The DMEM included high glucose medium with 10% fetal bovine serum ( FBS ; Thermo Fisher Scientific, Inc., Waltham, MA), 2% chicken serum, 1% sodium pyruvate, 1% glutamax, 1% non-essential amino acids ( NEAA ; Thermo Fisher Scientific, Inc., Waltham, MA), 10 μg/mL leukocyte inhibitory factor ( LIF ; Thermo Fisher Scientific, Inc., Waltham, MA), 10 μg/mL stem cell growth factor ( SCF ; Thermo Fisher Scientific, Inc., Waltham, MA), and 50 μg/mL fibroblast growth factor 2 ( FGF2 ; Thermo Fisher Scientific, Inc., Waltham, MA). cESCs’ cultural medium was changed every 2 d, and passaging was done every 3 d. Cells were visualized under a bright-field phase-contrast microscope (Nikon-Eclipse TE 2000-S).

    Techniques: Infection, Microscopy, Concentration Assay, Western Blot