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gc ms analysis  (MACHEREY NAGEL)


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    MACHEREY NAGEL gc ms analysis
    Gc Ms Analysis, supplied by MACHEREY NAGEL, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Gas Chromatography-Mass Spectrometry:

    Article Title: A plastid carbohydrate carrier mediates ribose recycling from nucleotide catabolism and glucose export from starch degradation
    Article Snippet: Samples were incubated at 37 °C and 950 rpm for 2 h. Next, 70 μL MSFTA reagent (Macherey & Nagel, 701270.110) was added to each sample, which was further incubated at 37 °C and 950 rpm for 30 min. .. Samples were transferred to glass vials suitable for GC-MS analysis (Macherey & Nagel, 702891 and 702730). ..

    Article Title: A plastid carbohydrate carrier mediates ribose recycling from nucleotide catabolism and glucose export from starch degradation.
    Article Snippet: Samples were incubated at 37 °C and 950 rpm for 2 h. Next, 70 μL MSFTA reagent (Macherey & Nagel, 701270.110) was added to each sample, which was further incubatedat 37 °Cand950 rpmfor30min. .. Sampleswere transferred toglass vials suitable for GC-MS analysis (Macherey & Nagel, 702891 and 702730). ..



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    Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Journal: Bioactive Materials

    Article Title: Reconstructing the ischemic osteogenic microenvironment through hierarchical scaffolds orchestrating Mg 2+ signaling and neuropilin-1–mediated angiogenesis

    doi: 10.1016/j.bioactmat.2026.02.031

    Figure Lengend Snippet: Evaluation of angiogenic potential induced by Mg 2+ and NRP-1. ( A ) Scratch assay in three different microenvironments. ( B ) Transwell assay in three different microenvironments. ( C ) Quantitative analysis of wound healing area. ( D ) Quantitative analysis of number of migration cells. ( E ) Immunofluorescence staining of VEGFA and FGF2, with DAPI for nuclear staining and F-actin for cytoskeleton labeling. ( F ) Tube formation evaluation in four different microenvironments. ( G ) Quantitative analysis of number of junction. ( H ) Quantitative analysis of Flu intensity. ( I ) Western-blot analysis of VEGFA, FGF2, and Nr4a1. ( J-L ) Quantitative analysis of relative protein expression of VEGFA, FGF2, and Nr4a1. Data are presented as mean values ± s.d. (n = 3). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001 (one-way ANOVA).

    Article Snippet: For the Transwell assay, BMSCs were seeded in the upper chambers of Transwell inserts (8.0 μm pore size; Servicebio, China), while different culture conditions were applied in the lower chambers according to the experimental groups.

    Techniques: Wound Healing Assay, Transwell Assay, Migration, Immunofluorescence, Staining, Labeling, Western Blot, Expressing