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vitronectin protein  (MedChemExpress)


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    MedChemExpress vitronectin protein
    Vitronectin Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/vitronectin protein/product/MedChemExpress
    Average 94 stars, based on 12 article reviews
    vitronectin protein - by Bioz Stars, 2026-03
    94/100 stars

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    Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of <t>vitronectin-</t> and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also <xref ref-type= Supplementary Figure 1 . " width="250" height="auto" />
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    Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of <t>vitronectin-</t> and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also <xref ref-type= Supplementary Figure 1 . " width="250" height="auto" />
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    Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of <t>vitronectin-</t> and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also <xref ref-type= Supplementary Figure 1 . " width="250" height="auto" />
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    Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of <t>vitronectin-</t> and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also <xref ref-type= Supplementary Figure 1 . " width="250" height="auto" />
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    Image Search Results


    Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of vitronectin- and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also <xref ref-type= Supplementary Figure 1 . " width="100%" height="100%">

    Journal: Frontiers in Cellular and Infection Microbiology

    Article Title: Biological boundary conditions regulate the internalization of Aspergillus fumigatus conidia by alveolar cells

    doi: 10.3389/fcimb.2025.1515779

    Figure Lengend Snippet: Internalization of A fumigatus conidia in a subpopulation of Lamp + Actin + vesicles in cells on circular micropatterns and effect of ECM composition on conidia internalization. (A) Representative example of two cells on fibronectin-coated circular micropattern (28 µm). Overview of Lamp1 and Actin is shown as maximal Z-projection of FITC/TRITC channels of 9 focal planes. Magnified images show conidia in Lamp1 + (green) and Lamp1 + Actin + vesicles (red and green) 3 hours post-infection. Scale bars = 10 µm. (B) Percentage of conidia internalized in Lamp1 + Actin + vesicles relative to the total conidia number in cells constrained on fibronectin-coated circular micropatterns with different sizes and cell density at 1 and 3 hours post-infection. (C) Conidia spatial distribution map of 50 overlaid micropatterns displaying Lamp1 + Actin + vesicles with internalized conidia (green spheres in red circles). (D) Comparison of vitronectin- and fibronectin micropatterns. Quantification of the average number of total conidia and the percentage of conidia internalized in Lamp1 + and Lamp1 + Actin + vesicles at 1 and 3 hours post-infection relative to the total conidia number. **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001; ns P > 0.05. VN, vitronectin; FN, fibronectin. See also Supplementary Figure 1 .

    Article Snippet: The patterned substrates were subsequently incubated with 150 μl of fibronectin (10 μg/ml, Sigma Aldrich, 341631, Austria) in PBS or vitronectin (3.3 μl/ml, ProSci, 91-362, USA) at 4°C overnight and washed once with PBS.

    Techniques: Infection, Comparison

    Journal: eLife

    Article Title: Complete suspension culture of human induced pluripotent stem cells supplemented with suppressors of spontaneous differentiation

    doi: 10.7554/eLife.89724

    Figure Lengend Snippet:

    Article Snippet: To prepare enough hiPSCs to start large-scale culture, hiPSCs were pre-cultured in iMatrix-511MG (Cat#892005, Matrixome) or Vitronectin (VTN-N) Recombinant Human Protein, Truncated (Cat#A14700, Thermo Fisher Scientific)-coated cell culture flasks with StemFitAK03N (Cat#AK03N, Ajinomoto) including 20 μM IWR-1-endo and 1 μM LY333531.

    Techniques: Recombinant, Suspension, Plasmid Preparation