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inverted fluorescent microscope nikon eclipse te2000-u  (Nikon)


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    Nikon inverted fluorescent microscope nikon eclipse te2000-u
    Inverted Fluorescent Microscope Nikon Eclipse Te2000 U, 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/fluorescence+microscope+nikon+eclipse+te2000-u/pm40250144-42-14-16
    Average 90 stars, based on 1 article reviews
    inverted fluorescent microscope nikon eclipse te2000-u - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Investigation of Dextran-Coated Magnetic Nanoparticles Encapsulated by medication and modified with Folate for Targeted drug delivery: Invito and docking studies
    Article Snippet: • Fe3O4@DEX-CP-FA NPs were produced by the chemical.. • We measured the size of the nanoparticle by using DLS, AFM, SEM, and

    Article Title: Gas6 induces AIM to suppress acute lung injury in mice by inhibiting NLRP3 inflammasome activation and inducing autophagy
    Article Snippet: Cells were visualized using a fluorescence microscope (Nikon ECLIPSE TE2000-U, Nikon Instruments Inc., Melville, NY, USA).

    Article Title: Positively-charged, chalcone-hydroxypyrone hybrid ruthenium(II)-arene complexes functionalized with ethacrynic acid: Synthesis, characterizaion, and antitumor effect.
    Article Snippet: A new family of ethacrynic acid-functionalized, chalcone-hydroxypyrone hybrid ruthenium(II)-arene complexes (4a-4e) have been designed, synthesis and fully characterized by 1H and 13C NMR, ESI-MS, elemental analysis, and melting point tests.. The molecular structure of 3a, one of the precursor complexes, has been determined by single-crystal X-ray diffraction.. The cytotoxicity of the obtained complexes toward human cancer cell lines such as HeLa, MGC803, A549, MDA-MB-231, and MCF-7 cells have been investigated by MTT assay.

    Article Title: Synthesis and comparison of cationic polymers for structural effects of backbones and grafted side chains on their <scp>DNA</scp> transfection for efficient gene delivery
    Article Snippet: Many cationic polymers with varied architectures either in backbones or in side chains have been used for gene delivery.. However, these polymers yielding different DNA transfection efficiency cannot answer whether backbones or side chains havemore influence on DNA delivery.. In this research, polyurethanes (PUs) made from the reaction of L-lysine diisocyanate and 1,4-piperazinediethanol were synthesized.

    Article Title: Bison, Elk, and Other Captive Wildlife Species Humoral Immune Responses against SARS-CoV-2.
    Article Snippet: Following incubation, plates were washed two times with PBS-T and observed under a fluorescence microscope (Nikon ECLIPSE TE2000-U, Nikon, Yokohama, Japan) to determine endpoint titer to BCoV based on the presence or absence of viral replication.

    Fluorescence:

    Article Title: Calpastatin, a calpain specific inhibitor, reduce seizures in a mouse model of temporal lobe epilepsy
    Article Snippet: After staining, tissue sections were mounted on slides using Vectorshield (Vector Labs). .. Images were obtained using a Nikon Eclipse TE2000‐U fluorescence microscope. .. To detect αII‐spectrin breakdown products (SBDP) as an indicator of calpain activation, brain sections were incubated with a rabbit polyclonal anti‐αII‐spectrin N‐terminal fragment (SNTF) antibody (1:200, Sigma Cat. No. ABN2264).

    Article Title: Inhibition of Mettl3 by STM2457 and Loss of Macrophage Mettl3 Alleviate Pulmonary Hypertension and Right Heart Remodeling.
    Article Snippet: Background m6A RNA methylation is a critical epigenetic modification involved in the pathogenesis of pulmonary arterial hypertension (PAH).. While macrophage-mediated inflammation plays a central role in PAH, the specific contributions of m6A regulators within macrophages are not yet fully understood.. This study explores the role of METTL3 in macrophages, with particular emphasis on its contribution to the progression of PAH.

    Article Title: The toxicity of superparamagnetic iron oxide nanoparticles induced on the testicular cells: In vitro study.
    Article Snippet: Superparamagnetic iron oxide nanoparticles (SPIONs) have gained significant attention in biomedical research due to their potential applications.. However, little is known about their impact and toxicity on testicular cells.. To address this issue, we conducted an in vitro study using primary mouse testicular cells, testis fragments, and sperm to investigate the cytotoxic effects of sodium citrate-coated SPIONs (Cit_SPIONs).

    Microscopy:

    Article Title: Calpastatin, a calpain specific inhibitor, reduce seizures in a mouse model of temporal lobe epilepsy
    Article Snippet: After staining, tissue sections were mounted on slides using Vectorshield (Vector Labs). .. Images were obtained using a Nikon Eclipse TE2000‐U fluorescence microscope. .. To detect αII‐spectrin breakdown products (SBDP) as an indicator of calpain activation, brain sections were incubated with a rabbit polyclonal anti‐αII‐spectrin N‐terminal fragment (SNTF) antibody (1:200, Sigma Cat. No. ABN2264).

    Article Title: Inhibition of Mettl3 by STM2457 and Loss of Macrophage Mettl3 Alleviate Pulmonary Hypertension and Right Heart Remodeling.
    Article Snippet: Background m6A RNA methylation is a critical epigenetic modification involved in the pathogenesis of pulmonary arterial hypertension (PAH).. While macrophage-mediated inflammation plays a central role in PAH, the specific contributions of m6A regulators within macrophages are not yet fully understood.. This study explores the role of METTL3 in macrophages, with particular emphasis on its contribution to the progression of PAH.

    Article Title: The toxicity of superparamagnetic iron oxide nanoparticles induced on the testicular cells: In vitro study.
    Article Snippet: Superparamagnetic iron oxide nanoparticles (SPIONs) have gained significant attention in biomedical research due to their potential applications.. However, little is known about their impact and toxicity on testicular cells.. To address this issue, we conducted an in vitro study using primary mouse testicular cells, testis fragments, and sperm to investigate the cytotoxic effects of sodium citrate-coated SPIONs (Cit_SPIONs).

    Imaging:

    Article Title: The toxicity of superparamagnetic iron oxide nanoparticles induced on the testicular cells: In vitro study.
    Article Snippet: Superparamagnetic iron oxide nanoparticles (SPIONs) have gained significant attention in biomedical research due to their potential applications.. However, little is known about their impact and toxicity on testicular cells.. To address this issue, we conducted an in vitro study using primary mouse testicular cells, testis fragments, and sperm to investigate the cytotoxic effects of sodium citrate-coated SPIONs (Cit_SPIONs).



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    Nikon fluorescent microscope nikon eclipse te2000-u
    RUXO does not protect against pilocarpine-induced acute or chronic neuronal loss nor mossy fiber sprouting. ( a ) Representative images of Fluoro-Jade B (FJB)-stained DG, CA1 and CA3 subregions. Mounted coronal brain sections (14 ​μm) were stained with FJB to selectively stain dying neurons 48 ​h post-SE. Approximately 10 sections from a 1-in-20 series of sections from each brain (SE- RUXO, n ​= ​3; SE-DMSO, n ​= ​3) were processed. ( b ) FJB-positive cells were counted blindly within standardized areas of the DG, CA1 and CA3 regions of the hippocampus using ImageJ Analysis software (v. 1.53a). Number of FJB-positive cells in DG, CA1, or CA3, are reported as mean ​± ​SEM. Statistical analysis was performed with either unpaired Student's t -test (DG and CA3), or Mann-Whintey (CA1). ( c ) Representative images of ZnT3 staining in DG 4 weeks after SE induction. ( d ) ZnT3 immunoreactivity was quantified in the inner molecular layers of the upper and lower blades of the DG in 3 sections (from anterior to posterior) and values averaged. Sham animals showed no labeling in upper or lower DG while pilocarpine-injected rats showed presence of ZnT3 <t>fluorescent</t> staining indicative of mossy fiber sprouting (MFS). No statistically significant difference was observed in ZnT3 staining intensity between DMSO- (n ​= ​3) and RUXO-treated (n ​= ​3) rats by one-way ANOVA followed by Fisher's LSD post-hoc test. All images were taken with a Nikon Eclipse TE2000-U fluorescent <t>microscope</t> at 10x magnification. Fluorescence intensity was quantified with ImageJ on 16 bit-converted images.
    Fluorescent Microscope Nikon Eclipse Te2000 U, 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
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    Image Search Results


    RUXO does not protect against pilocarpine-induced acute or chronic neuronal loss nor mossy fiber sprouting. ( a ) Representative images of Fluoro-Jade B (FJB)-stained DG, CA1 and CA3 subregions. Mounted coronal brain sections (14 ​μm) were stained with FJB to selectively stain dying neurons 48 ​h post-SE. Approximately 10 sections from a 1-in-20 series of sections from each brain (SE- RUXO, n ​= ​3; SE-DMSO, n ​= ​3) were processed. ( b ) FJB-positive cells were counted blindly within standardized areas of the DG, CA1 and CA3 regions of the hippocampus using ImageJ Analysis software (v. 1.53a). Number of FJB-positive cells in DG, CA1, or CA3, are reported as mean ​± ​SEM. Statistical analysis was performed with either unpaired Student's t -test (DG and CA3), or Mann-Whintey (CA1). ( c ) Representative images of ZnT3 staining in DG 4 weeks after SE induction. ( d ) ZnT3 immunoreactivity was quantified in the inner molecular layers of the upper and lower blades of the DG in 3 sections (from anterior to posterior) and values averaged. Sham animals showed no labeling in upper or lower DG while pilocarpine-injected rats showed presence of ZnT3 fluorescent staining indicative of mossy fiber sprouting (MFS). No statistically significant difference was observed in ZnT3 staining intensity between DMSO- (n ​= ​3) and RUXO-treated (n ​= ​3) rats by one-way ANOVA followed by Fisher's LSD post-hoc test. All images were taken with a Nikon Eclipse TE2000-U fluorescent microscope at 10x magnification. Fluorescence intensity was quantified with ImageJ on 16 bit-converted images.

    Journal: Neurotherapeutics

    Article Title: Ruxolitinib-dependent reduction of seizure load and duration is accompanied by spatial memory improvement in the rat pilocarpine model of temporal lobe epilepsy

    doi: 10.1016/j.neurot.2024.e00506

    Figure Lengend Snippet: RUXO does not protect against pilocarpine-induced acute or chronic neuronal loss nor mossy fiber sprouting. ( a ) Representative images of Fluoro-Jade B (FJB)-stained DG, CA1 and CA3 subregions. Mounted coronal brain sections (14 ​μm) were stained with FJB to selectively stain dying neurons 48 ​h post-SE. Approximately 10 sections from a 1-in-20 series of sections from each brain (SE- RUXO, n ​= ​3; SE-DMSO, n ​= ​3) were processed. ( b ) FJB-positive cells were counted blindly within standardized areas of the DG, CA1 and CA3 regions of the hippocampus using ImageJ Analysis software (v. 1.53a). Number of FJB-positive cells in DG, CA1, or CA3, are reported as mean ​± ​SEM. Statistical analysis was performed with either unpaired Student's t -test (DG and CA3), or Mann-Whintey (CA1). ( c ) Representative images of ZnT3 staining in DG 4 weeks after SE induction. ( d ) ZnT3 immunoreactivity was quantified in the inner molecular layers of the upper and lower blades of the DG in 3 sections (from anterior to posterior) and values averaged. Sham animals showed no labeling in upper or lower DG while pilocarpine-injected rats showed presence of ZnT3 fluorescent staining indicative of mossy fiber sprouting (MFS). No statistically significant difference was observed in ZnT3 staining intensity between DMSO- (n ​= ​3) and RUXO-treated (n ​= ​3) rats by one-way ANOVA followed by Fisher's LSD post-hoc test. All images were taken with a Nikon Eclipse TE2000-U fluorescent microscope at 10x magnification. Fluorescence intensity was quantified with ImageJ on 16 bit-converted images.

    Article Snippet: All images were taken with a Nikon Eclipse TE2000-U fluorescent microscope at 10x magnification.

    Techniques: Staining, Software, Labeling, Injection, Microscopy, Fluorescence