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fluorescein conjugated uea 1 lectin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories fluorescein conjugated uea 1 lectin
    Fluorescein Conjugated Uea 1 Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 253 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fluorescein+conjugated+uea+1+lectin/Fluorescein+labeled+Ulex+Europaeus+Agglutinin+I+(UEA+I)/pmc12577753-389-47-50
    Average 96 stars, based on 253 article reviews
    fluorescein conjugated uea 1 lectin - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Incubation:

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates.
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4◦C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061-2; 1:200). ..

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4°C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061–2; 1:200). ..

    Blocking Assay:

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates.
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4◦C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061-2; 1:200). ..

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4°C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061–2; 1:200). ..

    Staining:

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates.
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4◦C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061-2; 1:200). ..

    Article Title: Integration of phospho-signaling and transcriptomics in single cells reveals distinct Th17 cell fates
    Article Snippet: .. Sections were incubated with 1x PBS for 10 min and were then blocked with Trident Universal Protein Blocking Reagent (GeneTex; GTX30963) and 5% TruStain FcX PLUS at room temperature for 1 h. Slides were stained overnight at 4°C with a rabbit primary antibody to E-Cadherin (1:100) and fluorescein-conjugated UEA-1 Lectin (Vector Labs; FL-1061–2; 1:200). ..



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    Characterization of cultured human EPCs. PBMC-derived EPCs with a spindle shape formed clones (a) (200x). EPCs were shown to simultaneously endocytose DiI-ac-LDL (red) and bind fluorescein <t>isothiocyanate</t> UEA-1 <t>(lectin,</t> green), and a merged photo was also presented (b) (200x). FACS analysis showed high expression of CD133, CD34, and KDR on EPCs (c). Scale bar = 50 μ m.
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    Lineage tracing of cells with Lgr5 transcriptional activity in H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-Tom mice. 1-2-month old Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were treated with one i.p. injection of tamoxifen (0.1 mg/g body weight) and inoculated with H. felis two months post tamoxifen. Animals were analyzed 3 months after inoculation, and 5 months after tamoxifen injection. Gastric paraffin sections of the lesser curvature of H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were stained with anti-tomato (red fluorescent protein) primary antibodies and Alexa 555–conjugated secondary antibodies together with anti-IF antibodies and Alexa 488–conjugated secondary antibodies (IF/Tom), Alexa 488–conjugated GSII (GSII/Tom), Alexa 488–conjugated Ulex europaeus <t>agglutinin</t> <t>1</t> <t>(UEA1),</t> anti-CD44 and anti-CD44v9 primary antibodies and Alexa 488–conjugated secondary antibodies (CD44/Tom and CD44v9/Tom), and anti-BrdU primary antibodies and Alexa 488–conjugated secondary antibodies (BrdU/Tom). Scale bars : 50 μm. Similar results were observed in at least 5 other H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice except for the experiments with the anti-CD44v9 antibodies that were repeated in 1 other mouse.
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    Lineage tracing of cells with Lgr5 transcriptional activity in H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-Tom mice. 1-2-month old Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were treated with one i.p. injection of tamoxifen (0.1 mg/g body weight) and inoculated with H. felis two months post tamoxifen. Animals were analyzed 3 months after inoculation, and 5 months after tamoxifen injection. Gastric paraffin sections of the lesser curvature of H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were stained with anti-tomato (red fluorescent protein) primary antibodies and Alexa 555–conjugated secondary antibodies together with anti-IF antibodies and Alexa 488–conjugated secondary antibodies (IF/Tom), Alexa 488–conjugated GSII (GSII/Tom), Alexa 488–conjugated Ulex europaeus <t>agglutinin</t> <t>1</t> <t>(UEA1),</t> anti-CD44 and anti-CD44v9 primary antibodies and Alexa 488–conjugated secondary antibodies (CD44/Tom and CD44v9/Tom), and anti-BrdU primary antibodies and Alexa 488–conjugated secondary antibodies (BrdU/Tom). Scale bars : 50 μm. Similar results were observed in at least 5 other H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice except for the experiments with the anti-CD44v9 antibodies that were repeated in 1 other mouse.
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    Characterization of EPCs using fluorescence microscopy. (A) <t>FITC-UEA-1</t> positive cells identified by fluorescence staining with FITC-UEA-1. (B) Dil-Ac-LDL stained cells. (C) Nuclei counterstained with DAPI (D) Merged panels to reveal double-positive staining with Dil-Ac-LDL and FITC-UEA-1. EPCs, endothelial progenitor cells; FITC-UEA-1, fluorescein <t>isothiocyanate-conjugated</t> Ulex <t>europaeus</t> <t>lectin;</t> Dil-Ac-LDL, 1,1-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine-labeled acetylated low-density lipoprotein.
    Fluorescein Isothiocyanate Conjugated Ulex Europaeus Lectin (Fitc Uea 1, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Characterization of cultured human EPCs. PBMC-derived EPCs with a spindle shape formed clones (a) (200x). EPCs were shown to simultaneously endocytose DiI-ac-LDL (red) and bind fluorescein isothiocyanate UEA-1 (lectin, green), and a merged photo was also presented (b) (200x). FACS analysis showed high expression of CD133, CD34, and KDR on EPCs (c). Scale bar = 50 μ m.

    Journal: Oxidative Medicine and Cellular Longevity

    Article Title: Inhibition of Galectin-3 Alleviates Cigarette Smoke Extract-Induced Autophagy and Dysfunction in Endothelial Progenitor Cells

    doi: 10.1155/2019/7252943

    Figure Lengend Snippet: Characterization of cultured human EPCs. PBMC-derived EPCs with a spindle shape formed clones (a) (200x). EPCs were shown to simultaneously endocytose DiI-ac-LDL (red) and bind fluorescein isothiocyanate UEA-1 (lectin, green), and a merged photo was also presented (b) (200x). FACS analysis showed high expression of CD133, CD34, and KDR on EPCs (c). Scale bar = 50 μ m.

    Article Snippet: After 14 days of culture, the cells were incubated with fluorescein isothiocyanate-conjugated lectin from Ulex europaeus agglutinin 1 (FITC-UEA-1) (Sigma, Germany), and 1,19-dioctadecyl-3,3,3939-tetramethylindocar-bocyanine perchlorate-labeled acetylated low-density lipoprotein (LDL-ac-Dil) (Sigma, Germany).

    Techniques: Cell Culture, Derivative Assay, Clone Assay, Expressing

    Lineage tracing of cells with Lgr5 transcriptional activity in H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-Tom mice. 1-2-month old Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were treated with one i.p. injection of tamoxifen (0.1 mg/g body weight) and inoculated with H. felis two months post tamoxifen. Animals were analyzed 3 months after inoculation, and 5 months after tamoxifen injection. Gastric paraffin sections of the lesser curvature of H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were stained with anti-tomato (red fluorescent protein) primary antibodies and Alexa 555–conjugated secondary antibodies together with anti-IF antibodies and Alexa 488–conjugated secondary antibodies (IF/Tom), Alexa 488–conjugated GSII (GSII/Tom), Alexa 488–conjugated Ulex europaeus agglutinin 1 (UEA1), anti-CD44 and anti-CD44v9 primary antibodies and Alexa 488–conjugated secondary antibodies (CD44/Tom and CD44v9/Tom), and anti-BrdU primary antibodies and Alexa 488–conjugated secondary antibodies (BrdU/Tom). Scale bars : 50 μm. Similar results were observed in at least 5 other H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice except for the experiments with the anti-CD44v9 antibodies that were repeated in 1 other mouse.

    Journal: Cellular and Molecular Gastroenterology and Hepatology

    Article Title: Regulation of Gastric Lgr5+ve Cell Homeostasis by Bone Morphogenetic Protein (BMP) Signaling and Inflammatory Stimuli

    doi: 10.1016/j.jcmgh.2018.01.007

    Figure Lengend Snippet: Lineage tracing of cells with Lgr5 transcriptional activity in H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-Tom mice. 1-2-month old Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were treated with one i.p. injection of tamoxifen (0.1 mg/g body weight) and inoculated with H. felis two months post tamoxifen. Animals were analyzed 3 months after inoculation, and 5 months after tamoxifen injection. Gastric paraffin sections of the lesser curvature of H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice were stained with anti-tomato (red fluorescent protein) primary antibodies and Alexa 555–conjugated secondary antibodies together with anti-IF antibodies and Alexa 488–conjugated secondary antibodies (IF/Tom), Alexa 488–conjugated GSII (GSII/Tom), Alexa 488–conjugated Ulex europaeus agglutinin 1 (UEA1), anti-CD44 and anti-CD44v9 primary antibodies and Alexa 488–conjugated secondary antibodies (CD44/Tom and CD44v9/Tom), and anti-BrdU primary antibodies and Alexa 488–conjugated secondary antibodies (BrdU/Tom). Scale bars : 50 μm. Similar results were observed in at least 5 other H felis –infected Lgr5-Cre;H + /K + -Nog;Rosa26-tdTom mice except for the experiments with the anti-CD44v9 antibodies that were repeated in 1 other mouse.

    Article Snippet: In some experiments the slides were stained for 1.5 hours at 37°C with Alexa 488–conjugated GSII (1:1000, catalog number: FL-1211; Vector Laboratories, Burlingame, CA) and fluorescein isothiocyanate–conjugated Ulex europaeus agglutinin 1 lectin (1:200, catalog number: FL-1061; Vector Laboratories).

    Techniques: Activity Assay, Infection, Injection, Staining

    Characterization of EPCs using fluorescence microscopy. (A) FITC-UEA-1 positive cells identified by fluorescence staining with FITC-UEA-1. (B) Dil-Ac-LDL stained cells. (C) Nuclei counterstained with DAPI (D) Merged panels to reveal double-positive staining with Dil-Ac-LDL and FITC-UEA-1. EPCs, endothelial progenitor cells; FITC-UEA-1, fluorescein isothiocyanate-conjugated Ulex europaeus lectin; Dil-Ac-LDL, 1,1-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine-labeled acetylated low-density lipoprotein.

    Journal: Molecular Medicine Reports

    Article Title: Generation of an anti-angiogenic endothelial progenitor cell line via endostatin gene transfer

    doi: 10.3892/mmr.2018.8623

    Figure Lengend Snippet: Characterization of EPCs using fluorescence microscopy. (A) FITC-UEA-1 positive cells identified by fluorescence staining with FITC-UEA-1. (B) Dil-Ac-LDL stained cells. (C) Nuclei counterstained with DAPI (D) Merged panels to reveal double-positive staining with Dil-Ac-LDL and FITC-UEA-1. EPCs, endothelial progenitor cells; FITC-UEA-1, fluorescein isothiocyanate-conjugated Ulex europaeus lectin; Dil-Ac-LDL, 1,1-dioctadecyl-3,3,3′,3′-tetramethylindocarbocyanine-labeled acetylated low-density lipoprotein.

    Article Snippet: Subsequently, cells were fixed by 4% polyoxymethylene at room temperature for 20 min and counterstained with fluorescein isothiocyanate-conjugated Ulex europaeus lectin (FITC-UEA-1; 10 µg/ml; cat. no. L9006; Sigma-Aldrich; Merck KGaA) for 1 h at room temperature.

    Techniques: Fluorescence, Microscopy, Staining, Labeling

    Determination of the expression of EPC surface markers via flow-cytometry. (A) CD31 and FLK-1 expression, and (B) CD34 and CD133 expression. EPCs, endothelial progenitor cells; FITC, fluorescein isothiocyanate; PE, phycoerythrin; FLK-1, fetal liver kinase-1; CD, cluster of differentiation.

    Journal: Molecular Medicine Reports

    Article Title: Generation of an anti-angiogenic endothelial progenitor cell line via endostatin gene transfer

    doi: 10.3892/mmr.2018.8623

    Figure Lengend Snippet: Determination of the expression of EPC surface markers via flow-cytometry. (A) CD31 and FLK-1 expression, and (B) CD34 and CD133 expression. EPCs, endothelial progenitor cells; FITC, fluorescein isothiocyanate; PE, phycoerythrin; FLK-1, fetal liver kinase-1; CD, cluster of differentiation.

    Article Snippet: Subsequently, cells were fixed by 4% polyoxymethylene at room temperature for 20 min and counterstained with fluorescein isothiocyanate-conjugated Ulex europaeus lectin (FITC-UEA-1; 10 µg/ml; cat. no. L9006; Sigma-Aldrich; Merck KGaA) for 1 h at room temperature.

    Techniques: Expressing, Flow Cytometry