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transmission electron microscope carl zeiss leo em912 omega  (Carl Zeiss)


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    Structured Review

    Carl Zeiss transmission electron microscope carl zeiss leo em912 omega
    Transmission Electron Microscope Carl Zeiss Leo Em912 Omega, supplied by Carl Zeiss, 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/em912+electron+microscope/912+electron+em+microscope/pm39190872-95-10-15
    Average 90 stars, based on 1 article reviews
    transmission electron microscope carl zeiss leo em912 omega - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: γ-Fe 2 O 3 @Zn-LDH-EAE-SO 3 H for multi-component synthesis of chromeno[4,3- b ]quinoline-6,8-dione derivatives
    Article Snippet: Transmission electron microscopy (TEM) was performed using a Leo 912 AB microscope (Zeiss, Germany) at an accelerating voltage of 120 kV.

    Article Title: A translational protocol optimizes the isolation of plasma-derived extracellular vesicle proteomics.
    Article Snippet: The following secondary antibodies were used: Peroxidase conjugated AffiniPure goat anti-mouse IgG (Jackson ImmunoResearch Laboratories, 115-035-003, 1:10,000) and Peroxidase conjugated AffiniPure goat anti-rabbit IgG (Jackson ImmunoResearch Laboratories, 111-035-003, 1:10,000).

    Article Title: Complexome profiling of the Chlamydomonas psb28 mutant reveals TEF5 as an early PSII assembly factor
    Article Snippet: The samples were then embedded in Epon 812 resin and polymerized at 63 °C for 48 h. Ultrathin sections (50-nm thickness) were prepared with a 35° diamond knife (DiATOME, Nidau, Switzerland) on an Ultracut E ultramicrotome (Leica Microsystems).

    Article Title: ZIF-8/doxorubicin nanoparticles camouflaged with Cucurbita -derived exosomes for targeted prostate cancer therapy.
    Article Snippet: Development of biomimetic drug delivery systems (DDSs) holds great promise to overcome various nanoparticle-associated hindrances in cancer therapy.. However, producing biomimetic nanoparticles camouflaged by animal cell-secreted exosomes presents several challenges, including low yield and some ethical considerations.. Herein, we designed a biomimetic nanocarrier composed of zeolitic imidazolate framework-8 (ZIF-8) encapsulating doxorubicin (DOX) as the core and a shell of exosome-like nanoparticles (EXO) derived from Cucurbita moschata (CEXO).

    Article Title: Characterization of a plasmid dependent DNA phage targeting Escherichia coli harboring a conjugative plasmid and its impact on gut microbiota.
    Article Snippet: The phages were then observed using a TEM (Carl Zeiss LEO 913AB) at an accelerating voltage of 80 kV at the National Instrumentation Center for Environmental Management in Seoul, Republic of Korea.

    Transmission Assay:

    Article Title: Complexation with chicken yolk phosvitin modulates antibacterial activity of chitosan.
    Article Snippet: In this study, it is shown for the first time that complexation with phosvitin does not restrict bacteriostatic activity of chitosan.. Moreover, chitosan possesses the activity in the presence of phosvitin in acidic and alkalescent media.. Besides, minimal inhibition concentrations of chitosan decrease in both acidic (pH 5.8) and alkalescent (pH 7.4) media, and chitosan shows two/fourfold higher bacteriostatic activity at 0.25–1.0 mg/ml phosvitin concentration in solution compared with that of chitosan alone due to an additive effect of chitosan and phosvitin, i.e. phosvitin modulates antimicrobial activity of chitosan in the acidic and alkalescent media.

    Microscopy:

    Article Title: Complexation with chicken yolk phosvitin modulates antibacterial activity of chitosan.
    Article Snippet: In this study, it is shown for the first time that complexation with phosvitin does not restrict bacteriostatic activity of chitosan.. Moreover, chitosan possesses the activity in the presence of phosvitin in acidic and alkalescent media.. Besides, minimal inhibition concentrations of chitosan decrease in both acidic (pH 5.8) and alkalescent (pH 7.4) media, and chitosan shows two/fourfold higher bacteriostatic activity at 0.25–1.0 mg/ml phosvitin concentration in solution compared with that of chitosan alone due to an additive effect of chitosan and phosvitin, i.e. phosvitin modulates antimicrobial activity of chitosan in the acidic and alkalescent media.



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