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andulex europeaus 1 lectin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories andulex europeaus 1 lectin
    Andulex Europeaus 1 Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 472 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/andulex europeaus 1 lectin/product/Vector Laboratories
    Average 96 stars, based on 472 article reviews
    andulex europeaus 1 lectin - by Bioz Stars, 2026-03
    96/100 stars

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    A serial cross section showing capillary staining. Capillaries are stained brown and are located at the peripheries of the myocyte. (Capillaries have been stained with Ulex Europeaus Agglutinin 1, 1:200, Vector laboratories, UK, visualised at magnification × 40 and are arrowed)
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    Millipore fluorescein isothiocyanate-conjugated lectin ulex europeaus agglutinin-1 (uea-1
    A serial cross section showing capillary staining. Capillaries are stained brown and are located at the peripheries of the myocyte. (Capillaries have been stained with Ulex Europeaus Agglutinin 1, 1:200, Vector laboratories, UK, visualised at magnification × 40 and are arrowed)
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    Biomeda corporation ulex europeaus lectin 1
    A: phase-contrast and fluorescent images of a cord blood-derived “late” endothelial progenitor cell (EPC) colony. Endothelial cells derived from the long-term culture of mononuclear cells (at least 2–4 wk) can form highly proliferative colonies derived from single circulating endothelial cells. Left: phase-contrast image of an EPC colony derived from umbilical cord blood mononuclear cells. Right: confocal microscopy image of an endothelial colony stained with the endothelial surface stain Ulex europaeus lectin (green = fluorescein <t>isothiocyanate</t> label), the nucleus stain 4′,6-diamidino-2-phenylindole (blue) as well as uptake of acetylated low density lipoprotein (red = DiI label). B and C: flow cytometry phenotyping of EPCs using the endothelial surface marker CD31 [platelet endothelial cell adhesion molecule (PECAM)] and the myeloid surface marker CD45. Late EPCs (or colony-forming EPCs) derived from the long-term culture (at least 3–4 wk) of circulating mononuclear cells from adult blood and umbilical cord blood are positive for the endothelial marker CD31 (PECAM) but not for the myeloid marker CD45 while “early” EPCs [or cultured carcinogenic cells (CACs)] derived from the short-term culture (4 days) of adult mononuclear cells also express the myeloid marker CD45. The negative isotype control antibody staining is shown in gray.
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    Vector Laboratories lectin ulex europeaus agglutinin 1
    A: phase-contrast and fluorescent images of a cord blood-derived “late” endothelial progenitor cell (EPC) colony. Endothelial cells derived from the long-term culture of mononuclear cells (at least 2–4 wk) can form highly proliferative colonies derived from single circulating endothelial cells. Left: phase-contrast image of an EPC colony derived from umbilical cord blood mononuclear cells. Right: confocal microscopy image of an endothelial colony stained with the endothelial surface stain Ulex europaeus lectin (green = fluorescein <t>isothiocyanate</t> label), the nucleus stain 4′,6-diamidino-2-phenylindole (blue) as well as uptake of acetylated low density lipoprotein (red = DiI label). B and C: flow cytometry phenotyping of EPCs using the endothelial surface marker CD31 [platelet endothelial cell adhesion molecule (PECAM)] and the myeloid surface marker CD45. Late EPCs (or colony-forming EPCs) derived from the long-term culture (at least 3–4 wk) of circulating mononuclear cells from adult blood and umbilical cord blood are positive for the endothelial marker CD31 (PECAM) but not for the myeloid marker CD45 while “early” EPCs [or cultured carcinogenic cells (CACs)] derived from the short-term culture (4 days) of adult mononuclear cells also express the myeloid marker CD45. The negative isotype control antibody staining is shown in gray.
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    Biomeda corporation fluorescein-ulex europeaus lectin 1
    A: phase-contrast and fluorescent images of a cord blood-derived “late” endothelial progenitor cell (EPC) colony. Endothelial cells derived from the long-term culture of mononuclear cells (at least 2–4 wk) can form highly proliferative colonies derived from single circulating endothelial cells. Left: phase-contrast image of an EPC colony derived from umbilical cord blood mononuclear cells. Right: confocal microscopy image of an endothelial colony stained with the endothelial surface stain Ulex europaeus lectin (green = fluorescein <t>isothiocyanate</t> label), the nucleus stain 4′,6-diamidino-2-phenylindole (blue) as well as uptake of acetylated low density lipoprotein (red = DiI label). B and C: flow cytometry phenotyping of EPCs using the endothelial surface marker CD31 [platelet endothelial cell adhesion molecule (PECAM)] and the myeloid surface marker CD45. Late EPCs (or colony-forming EPCs) derived from the long-term culture (at least 3–4 wk) of circulating mononuclear cells from adult blood and umbilical cord blood are positive for the endothelial marker CD31 (PECAM) but not for the myeloid marker CD45 while “early” EPCs [or cultured carcinogenic cells (CACs)] derived from the short-term culture (4 days) of adult mononuclear cells also express the myeloid marker CD45. The negative isotype control antibody staining is shown in gray.
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    Image Search Results


    A serial cross section showing capillary staining. Capillaries are stained brown and are located at the peripheries of the myocyte. (Capillaries have been stained with Ulex Europeaus Agglutinin 1, 1:200, Vector laboratories, UK, visualised at magnification × 40 and are arrowed)

    Journal: BMC Geriatrics

    Article Title: Skeletal muscle morphology in sarcopenia defined using the EWGSOP criteria: findings from the Hertfordshire Sarcopenia Study (HSS)

    doi: 10.1186/s12877-015-0171-4

    Figure Lengend Snippet: A serial cross section showing capillary staining. Capillaries are stained brown and are located at the peripheries of the myocyte. (Capillaries have been stained with Ulex Europeaus Agglutinin 1, 1:200, Vector laboratories, UK, visualised at magnification × 40 and are arrowed)

    Article Snippet: Capillaries were stained by incubating separate slides with biotinylated Lectin Ulex Europeaus Agglutinin 1 (UEA-1, Vector Laboratories, Peterborough, UK) at a dilution of 1:200 for two hours (Fig. ).

    Techniques: Staining, Plasmid Preparation

    A: phase-contrast and fluorescent images of a cord blood-derived “late” endothelial progenitor cell (EPC) colony. Endothelial cells derived from the long-term culture of mononuclear cells (at least 2–4 wk) can form highly proliferative colonies derived from single circulating endothelial cells. Left: phase-contrast image of an EPC colony derived from umbilical cord blood mononuclear cells. Right: confocal microscopy image of an endothelial colony stained with the endothelial surface stain Ulex europaeus lectin (green = fluorescein isothiocyanate label), the nucleus stain 4′,6-diamidino-2-phenylindole (blue) as well as uptake of acetylated low density lipoprotein (red = DiI label). B and C: flow cytometry phenotyping of EPCs using the endothelial surface marker CD31 [platelet endothelial cell adhesion molecule (PECAM)] and the myeloid surface marker CD45. Late EPCs (or colony-forming EPCs) derived from the long-term culture (at least 3–4 wk) of circulating mononuclear cells from adult blood and umbilical cord blood are positive for the endothelial marker CD31 (PECAM) but not for the myeloid marker CD45 while “early” EPCs [or cultured carcinogenic cells (CACs)] derived from the short-term culture (4 days) of adult mononuclear cells also express the myeloid marker CD45. The negative isotype control antibody staining is shown in gray.

    Journal:

    Article Title: Release of proinflammatory mediators and expression of proinflammatory adhesion molecules by endothelial progenitor cells

    doi: 10.1152/ajpheart.00665.2008

    Figure Lengend Snippet: A: phase-contrast and fluorescent images of a cord blood-derived “late” endothelial progenitor cell (EPC) colony. Endothelial cells derived from the long-term culture of mononuclear cells (at least 2–4 wk) can form highly proliferative colonies derived from single circulating endothelial cells. Left: phase-contrast image of an EPC colony derived from umbilical cord blood mononuclear cells. Right: confocal microscopy image of an endothelial colony stained with the endothelial surface stain Ulex europaeus lectin (green = fluorescein isothiocyanate label), the nucleus stain 4′,6-diamidino-2-phenylindole (blue) as well as uptake of acetylated low density lipoprotein (red = DiI label). B and C: flow cytometry phenotyping of EPCs using the endothelial surface marker CD31 [platelet endothelial cell adhesion molecule (PECAM)] and the myeloid surface marker CD45. Late EPCs (or colony-forming EPCs) derived from the long-term culture (at least 3–4 wk) of circulating mononuclear cells from adult blood and umbilical cord blood are positive for the endothelial marker CD31 (PECAM) but not for the myeloid marker CD45 while “early” EPCs [or cultured carcinogenic cells (CACs)] derived from the short-term culture (4 days) of adult mononuclear cells also express the myeloid marker CD45. The negative isotype control antibody staining is shown in gray.

    Article Snippet: To confirm the endothelial phenotype, adherent cells were incubated with DiI-labeled acetylated low density lipoprotein (LDL; Molecular Probes-Invitrogen, Carlsbad, CA) for 4 h, and, after fixation, they were incubated with the fluorescein isothiocyanate-labeled endothelial surface stain Ulex europeaus lectin 1 (Biomeda, Foster City, CA) for 1 h, as well as the nuclear 4′,6-diamidino-2-phenylindole stain (Molecular Probes-Invitrogen) for 15 min ( 25 ).

    Techniques: Derivative Assay, Confocal Microscopy, Staining, Flow Cytometry, Marker, Cell Culture