eclipse te300 inverted fluorescence phase contrast microscope (Nikon)
Nikon is a verified supplier 
99
Structured Review
Nikon
eclipse te300 inverted fluorescence phase contrast microscope
Eclipse Te300 Inverted Fluorescence Phase Contrast Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59597 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/eclipse+te300+inverted+microscope/Objectives/pmc12811465-194-7-6
Average 99 stars, based on 59597 article reviews
Eclipse Te300 Inverted Fluorescence Phase Contrast Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 59597 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/eclipse+te300+inverted+microscope/Objectives/pmc12811465-194-7-6
Average 99 stars, based on 59597 article reviews
eclipse te300 inverted fluorescence phase contrast microscope - by Bioz Stars,
2026-09
99/100 stars
Images
1) Product Images from "Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii"
Article Title: Comparative analysis of Borrelia’s Defence mechanisms and their impact on genetic manipulation of low-passage isolates of Borrelia afzelii and Borrelia garinii
Journal: Current Research in Microbial Sciences
doi: 10.1016/j.crmicr.2025.100543
Figure Legend Snippet: Fluorescence of spirochetes transformed with a GFP plasmid. B. afzelii #1192 transformed with in vitro methylated (a) and with unmethylated pBSV2_OspA_GFP (b). B. afzelii #1201 transformed with in vitro methylated (c) and with unmethylated pBSV2_OspA_GFP (d). B. garinii #1195 transformed with in vitro methylated pBSV2_OspA_GFP (e). B. garinii #1226 transformed with in vitro methylated pBSV2_OspA_GFP (f). All cultures were grown in modified BSK II medium at 34°C. All photos were taken using a Nikon Eclipse TE300 Inverted Fluorescence Phase Contrast Microscope using a 40x objective.
Techniques Used: Fluorescence, Transformation Assay, Plasmid Preparation, In Vitro, Methylation, Modification, Microscopy
Related Articles
Inverted Microscopy:Article Title: Exosomes are specialized vehicles to induce fibronectin assembly Article Snippet: Tissues underwent the antigen retrieval step again for 20 min if the same tissue would be subjected to multiple labeling before being mounted in ProLong Gold with DAPI (Thermo Fisher Scientific P36931). .. Images were collected using a Nikon Article Title: The T3SS structural and effector genes of Chlamydia trachomatis are expressed in distinct phenotypic cell forms Article Snippet: .. Inclusions were imaged using a Nikon Article Title: Discovery of a bell-shaped dose response curve to melanin-concentrating hormone in the 3T3-L1 adipocyte model: low-dose MCH facilitates adipogenesis Article Snippet: .. Phase contrast images were obtained soon after cell staining to reduce the loss of morphological detail using a Nikon Article Title: Echs1 -mediated histone crotonylation facilitates zygotic genome activation and expression of repetitive elements in early mammalian embryos Article Snippet: .. Using Nikon Article Title: M2-like macrophages derived from THP-1 cells promote myofibroblast differentiation of synovial fibroblasts in association with the TGF-β1/SMAD2/3 signaling pathway. Article Snippet: .. Phase contrast images of cells were captured using an Article Title: A positive allosteric modulator of the β 1 AR with antagonist activity for catecholaminergic polymorphic ventricular tachycardia Article Snippet: .. After pretreatment, cells were stimulated with isoproterenol (0.01–1 μM) or left untreated (basal condition) and plated immediately in an FHD rotational cell chamber (Ionoptix) mounted on a Nikon Article Title: Cannabinoid Receptor 2 Activating Antibodies: A Promising Therapeutic Strategy for Macrophage-Driven Fibro-Inflammatory Diseases Article Snippet: .. A Nikon Article Title: Comparison of Gold Nanoparticle and Fluorophore-conjugated Antibodies for Labeling Epitopes in Permeabilized Cells. Article Snippet: Immunohistochemistry (IHC) and immunofluorescence (IF) are longstanding diagnostic tools, offering crucial insights into the spatial distribution and expression patterns of biomolecules within tissues.1–3 Most commonly applied in immunostaining practices due to the high selectivity of antibodies to their respective antigen proteins, IHC and IF have many applications in diagnostic pathology and basic research due to the relative simplicity of the assay.4,5 These staining techniques can be run as a direct or indirect method, where the labeled antibodies are bound to the primary target or a primary antibody specific for the epitope of interest, respectively.6 As with any such test, false positives and cases of ambiguous staining occur.. Indirect methods lower false positives in IHC and IF assays through washing steps to remove unbound antibodies and multiple secondary antibodies bound to the primary, leading to higher signal to noise.6 1348502 JHCXXX10.1369/00221554251348502Nanoparticle Performance in ImmunocytochemistryBaugher et al. research-article2025 Staining:Article Title: Discovery of a bell-shaped dose response curve to melanin-concentrating hormone in the 3T3-L1 adipocyte model: low-dose MCH facilitates adipogenesis Article Snippet: .. Phase contrast images were obtained soon after cell staining to reduce the loss of morphological detail using a Nikon Software:Article Title: Discovery of a bell-shaped dose response curve to melanin-concentrating hormone in the 3T3-L1 adipocyte model: low-dose MCH facilitates adipogenesis Article Snippet: .. Phase contrast images were obtained soon after cell staining to reduce the loss of morphological detail using a Nikon Article Title: Comparison of Gold Nanoparticle and Fluorophore-conjugated Antibodies for Labeling Epitopes in Permeabilized Cells. Article Snippet: Immunohistochemistry (IHC) and immunofluorescence (IF) are longstanding diagnostic tools, offering crucial insights into the spatial distribution and expression patterns of biomolecules within tissues.1–3 Most commonly applied in immunostaining practices due to the high selectivity of antibodies to their respective antigen proteins, IHC and IF have many applications in diagnostic pathology and basic research due to the relative simplicity of the assay.4,5 These staining techniques can be run as a direct or indirect method, where the labeled antibodies are bound to the primary target or a primary antibody specific for the epitope of interest, respectively.6 As with any such test, false positives and cases of ambiguous staining occur.. Indirect methods lower false positives in IHC and IF assays through washing steps to remove unbound antibodies and multiple secondary antibodies bound to the primary, leading to higher signal to noise.6 1348502 JHCXXX10.1369/00221554251348502Nanoparticle Performance in ImmunocytochemistryBaugher et al. research-article2025 Injection:Article Title: Echs1 -mediated histone crotonylation facilitates zygotic genome activation and expression of repetitive elements in early mammalian embryos Article Snippet: .. Using Nikon |