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Motic Group ae31 inverted fluorescence microscope
Ae31 Inverted Fluorescence Microscope, supplied by Motic Group, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/inverted+microscope/ae31e+microscope+motic/pm42320124-70-18-22
Average 86 stars, based on 1 article reviews
ae31 inverted fluorescence microscope - by Bioz Stars, 2026-09
86/100 stars

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Related Articles

other:

Article Title: Exploring the role of neutrophils in inflammatory pain hypersensitivity via single-cell transcriptome profiling
Article Snippet: Purified neutrophils were cytospun at 5.5 × 103 rpm for 5 minutes, air-dried, stained with Giemsa solution, and imaged via an inverted microscope (Motic, Fujian, China).

Article Title: Pharmacological effects and mechanism of Maxing Shigan Decoction in the treatment of influenza A viral pneumonia.
Article Snippet: Ethnopharmacology relevance: Maxing Shigan Decoction (MXSGD), derived from the traditional Chinese medicine (TCM) classic Shang Han Lun, is recognized as an effective TCM herbal formula for treating respiratory diseases, although its precise molecular mechanisms against influenza A virus (IAV) have not yet been fully elucidated.. Aim of the study: This study aimed to clarify the pharmacological effects of MXSGD on IAV-infected pneumonia mouse models, with a particular focus on its regulatory mechanism through miR-1260.. Materials and methods: The chemical composition of MXSGD was analyzed using an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS).

Article Title: Antiviral effects and mechanism of Ma-Xing-Shi-Gan-San on porcine reproductive and respiratory syndrome virus
Article Snippet: After 72 h, two independent double-blind researchers assessed the cytopathic effect (CPE) using an inverted microscope (Motic, Xiamen, China).

Article Title: Microcystin-LR induces lung injury in mice through the NF-κB/NLRP3 pathway.
Article Snippet: Microcystin-LR (MC-LR) a cyclic toxin produced by cyanobacterial species is known to exert detrimental effects on various organs, including lung.. Several investigators demonstrated that MC-LR exerts pulmonary toxicity, but the underlying mechanisms remain unclear.. This study aimed to investigate whether exposure to MC-LR-induced lung inflammation and examine the underlying mechanisms.

Article Title: Integrating heparan sulfate mimetics into LbL nanofilms as extracellular matrix-like architectures to promote bone tissue regeneration
Article Snippet: Biomimetic surfaces are increasingly needed to enhance the effectiveness of biomaterials in bone tissue repair.. The Layer-by-Layer (LbL) technique is a particularly attractive method due to its versatility and ability to incorporate a wide range of bioactive molecules under mild conditions.. While numerous LbL systems have been developed, those integrating glycosaminoglycans (GAG) are often reported to rapidly degrade, which limits their potential in tissue integration.

Inverted Microscopy:

Article Title: Light induced transthylakoidal proton gradient is a key signal driving the downward migration of motile diatoms in sediments.
Article Snippet: .. Identification was conducted under a Motic AE31 Inverted Microscope using 1 mL of the assemblage placed in a Sedgewick-Rafter chamber. ..

Article Title: Experimental Study on Hybrid Additive and Subtractive Manufacturing Processes for Improving Surface Quality.
Article Snippet: .. The microstructure was examined using a Motic inverted microscope. ..



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Collagen alignment along the long axis of physical boundary is maintained despite YAP and ROCK inhibition. A) PLM imaging and color map analysis of collagen. B) Collagen intensity and coherency graphs. C) Immunohistochemistry for collagens I and II. Nuclei stained with hematoxylin. D) Heat map of <t>Brillouin</t> frequency shift. E) Brillouin frequency shift measurement. An ordinary one-way analysis of variance (ANOVA) with Tukey's multiple comparisons was used for statistical analysis (n = 3). Significance levels: ns = not significant, ∗∗∗∗p < 0.0001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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Image Search Results


Collagen alignment along the long axis of physical boundary is maintained despite YAP and ROCK inhibition. A) PLM imaging and color map analysis of collagen. B) Collagen intensity and coherency graphs. C) Immunohistochemistry for collagens I and II. Nuclei stained with hematoxylin. D) Heat map of Brillouin frequency shift. E) Brillouin frequency shift measurement. An ordinary one-way analysis of variance (ANOVA) with Tukey's multiple comparisons was used for statistical analysis (n = 3). Significance levels: ns = not significant, ∗∗∗∗p < 0.0001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Embedded cell-only bioprinting to engineer structurally aligned meniscal fibrocartilage

doi: 10.1016/j.mtbio.2026.103308

Figure Lengend Snippet: Collagen alignment along the long axis of physical boundary is maintained despite YAP and ROCK inhibition. A) PLM imaging and color map analysis of collagen. B) Collagen intensity and coherency graphs. C) Immunohistochemistry for collagens I and II. Nuclei stained with hematoxylin. D) Heat map of Brillouin frequency shift. E) Brillouin frequency shift measurement. An ordinary one-way analysis of variance (ANOVA) with Tukey's multiple comparisons was used for statistical analysis (n = 3). Significance levels: ns = not significant, ∗∗∗∗p < 0.0001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: Measurements were acquired using an inverted Brillouin microscope (Discoverer, CellSense Technologies GmbH, Berlin, Germany) equipped with a 780 nm laser and a 20X air objective (Olympus, NA 0.50, UPlanFI).

Techniques: Inhibition, Imaging, Immunohistochemistry, Staining