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fluorophore conjugated uea 1 lectin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories fluorophore conjugated uea 1 lectin
    Fluorophore Conjugated Uea 1 Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 522 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/uea+1/Biotinylated+Ulex+Europaeus+Agglutinin+I+(UEA+I)/10__1038_slash_s41467___026___78216___2-653-11-14
    Average 96 stars, based on 522 article reviews
    fluorophore conjugated uea 1 lectin - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Defining enteric bacterial pathogenesis using organoids: Citrobacter rodentium uses EspC, an atypical mucinolytic protease, to penetrate mouse colonic mucus.
    Article Snippet: .. The sections were stained with the following primary antibodies and lectins: rabbit anti-LPS (Bio-Rad, OBT0986) for C. rodentium, rabbit anti-Muc2 (Boster, A01212; Novus Biologicals, NBP1–31231), UEA-1 (Vector Laboratories, FL-1061), MALII (Vector Laboratories, B-1265-1) for mucus, and mouse anti-E-cadherin (BD Transduction Laboratories 610182) for IECs. .. The sections were stained with the following primary antibodies and lectins: rabbit anti-LPS (Bio-Rad, OBT0986) for C. rodentium, rabbit anti-Muc2 (Boster, A01212; Novus Biologicals, NBP1–31231), UEA-1 (Vector Laboratories, FL-1061), MALII (Vector Laboratories, B-1265-1) for mucus, and mouse anti-E-cadherin (BD Transduction Laboratories 610182) for IECs.

    Article Title: UBL3 Participates in the Early Stages of CD83‐Dependent CD4 + T Cell Selection
    Article Snippet: Absolute cell numbers were obtained using an internal microsphere counting standard (BD Biosciences). .. Cell suspensions were stained with antibodies specific for MHC II (M5/114.15.2, WEHI Antibody Facility, PE), CD45 (30‐F11, PerCP), CD326 (G8.8, APC‐Cy7), Ly51 (6C3, FITC) (all Biolegend), and UEA‐1 (Vector Laboratories, biotinylated, streptavidin PE‐Cy7) before acquisition with a BD LSR Fortessa flow cytometer. ..

    Article Title: UBL3 Participates in the Early Stages of CD83‐Dependent CD4 + T Cell Selection
    Article Snippet: Cells were run through magnetic LS columns to remove CD45 + cells (Miltenyi Biotec). .. Flowthrough was collected and stained with antibodies specific for CD45 (30‐F11, PE), CD326 (G8.8, APC‐Cy7), Ly51 (6C3, FITC) (all Biolegend) and UEA‐1 (Vector Laboratories, biotinylated, streptavidin PE‐Cy7) before sorting with a BD Influx cell sorter. ..

    Article Title: Defining enteric bacterial pathogenesis using organoids: Citrobacter rodentium uses EspC, an atypical mucinolytic protease, to penetrate mouse colonic mucus
    Article Snippet: .. The sections were stained with the following primary antibodies and lectins: rabbit anti-LPS (Bio-Rad, OBT0986) for C. rodentium , rabbit anti-Muc2 (Boster, A01212; Novus Biologicals, NBP1–31231), UEA-1 (Vector Laboratories, FL-1061), MALII (Vector Laboratories, B-1265-1) for mucus, and mouse anti-E-cadherin (BD Transduction Laboratories 610182) for IECs. .. The secondary antibodies for staining include: Alexa Fluor 568-conjugated donkey anti-rabbit IgG and Alexa Fluor 647-conjugated donkey anti-mouse IgG (Life Technologies).

    Immunopeptidomics:

    Article Title: UBL3 Participates in the Early Stages of CD83‐Dependent CD4 + T Cell Selection
    Article Snippet: Absolute cell numbers were obtained using an internal microsphere counting standard (BD Biosciences). .. Cell suspensions were stained with antibodies specific for MHC II (M5/114.15.2, WEHI Antibody Facility, PE), CD45 (30‐F11, PerCP), CD326 (G8.8, APC‐Cy7), Ly51 (6C3, FITC) (all Biolegend), and UEA‐1 (Vector Laboratories, biotinylated, streptavidin PE‐Cy7) before acquisition with a BD LSR Fortessa flow cytometer. ..

    Flow Cytometry:

    Article Title: UBL3 Participates in the Early Stages of CD83‐Dependent CD4 + T Cell Selection
    Article Snippet: Absolute cell numbers were obtained using an internal microsphere counting standard (BD Biosciences). .. Cell suspensions were stained with antibodies specific for MHC II (M5/114.15.2, WEHI Antibody Facility, PE), CD45 (30‐F11, PerCP), CD326 (G8.8, APC‐Cy7), Ly51 (6C3, FITC) (all Biolegend), and UEA‐1 (Vector Laboratories, biotinylated, streptavidin PE‐Cy7) before acquisition with a BD LSR Fortessa flow cytometer. ..

    Whole Genome Amplification:

    Article Title: Using MUC2 mucin producing tumorigenic human goblet-like cells to uncover functional properties of the mucus barrier.
    Article Snippet: Briefly, coverslips were washed in PBS, fixed with paraformaldehyde (4%) for 15 min at 37°C, washed with PBS, and permeabilized with 0.35% Triton for 5 min. After three washes with PBST (0.1% Tween-20 in PBS), coverslips were blocked for 1 h with donkey serum (5%), washed, and incubated overnight with antibodies for MUC2 (sc -515,106, Santa Cruz) or FCGBP (PAP389Hu01, Cloud-Clone) at 4°C in a humidified chamber. .. The next day, PBST was used to wash the coverslips prior to incubating with fluorescent secondary antibodies and DAPI (Life Technologies) for 1 h. Lectins were imaged with PNA (FL-1071, Vector Laboratories), DBA (FL-1031, Vector Laboratories), ConA (FL-1001, Vector Laboratories), SNA/ EBL (FL-1301, Vector Laboratories), UEA-1 (FL-1061, Vector Laboratories), and WGA (FL-1021, Vector Laboratories). .. For migration and proliferation studies, cells were counterstained with Paxillin (05–417, Millipore) or with EdU incorporation measured as per the manufacturer’s instructions (C10637, Thermo Fisher).

    Article Title: Using MUC2 mucin producing tumorigenic human goblet-like cells to uncover functional properties of the mucus barrier
    Article Snippet: Briefly, coverslips were washed in PBS, fixed with paraformaldehyde (4%) for 15 min at 37°C, washed with PBS, and permeabilized with 0.35% Triton for 5 min. After three washes with PBST (0.1% Tween-20 in PBS), coverslips were blocked for 1 h with donkey serum (5%), washed, and incubated overnight with antibodies for MUC2 (sc -515,106, Santa Cruz) or FCGBP (PAP389Hu01, Cloud-Clone) at 4°C in a humidified chamber. .. The next day, PBST was used to wash the coverslips prior to incubating with fluorescent secondary antibodies and DAPI (Life Technologies) for 1 h. Lectins were imaged with PNA (FL-1071, Vector Laboratories), DBA (FL-1031, Vector Laboratories), ConA (FL-1001, Vector Laboratories), SNA/EBL (FL-1301, Vector Laboratories), UEA-1 (FL-1061, Vector Laboratories), and WGA (FL-1021, Vector Laboratories). .. For migration and proliferation studies, cells were counterstained with Paxillin (05–417, Millipore) or with EdU incorporation measured as per the manufacturer’s instructions ( C10637 , Thermo Fisher).

    Article Title: In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation
    Article Snippet: Slides were then incubated in 99.5% ethanol for 5 min, then left to dry and circled with a PAP (liquid blocker) pen (Fisher Scientific). .. DAPI (10 μg/mL, Sigma Aldrich), UEA-1 (Fluorescein-labeled Ulex Europaeus Agglutinin I, 40 μg/mL, Vector Laboratories), and WGA (Rhodamine Red-X-labeled Wheat Germ Agglutinin, 30 μg/mL, Vector Laboratories) were applied to fully cover the samples (approximately 250 μL) and incubated in the dark at 4°C for 45 min. ..

    Article Title: In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation.
    Article Snippet: Paraffin was removed from sectioned slides through incubation at 60 ◦ C for 10 min, followed by 2x 10-min incubations in pre-warmed xylenes at 60 ◦ C. Slides were then incubated in 99.5% ethanol for 5 min, then left to dry and circled with a PAP (liquid blocker) pen (Fisher Scientific). .. 108 DAPI (10 μg/mL, Sigma Aldrich), UEA-1 (Fluorescein-labeled Ulex Europaeus Agglutinin I, 40 μg/mL, Vector Laboratories), and WGA (Rhodamine Red-X-labeled Wheat Germ Agglutinin, 30 μg/mL, Vector Laboratories) were applied to fully cover the samples (approximately 250 μL) and incubated in the dark at 4 ◦ C for 45 min. ..

    Incubation:

    Article Title: In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation
    Article Snippet: Slides were then incubated in 99.5% ethanol for 5 min, then left to dry and circled with a PAP (liquid blocker) pen (Fisher Scientific). .. DAPI (10 μg/mL, Sigma Aldrich), UEA-1 (Fluorescein-labeled Ulex Europaeus Agglutinin I, 40 μg/mL, Vector Laboratories), and WGA (Rhodamine Red-X-labeled Wheat Germ Agglutinin, 30 μg/mL, Vector Laboratories) were applied to fully cover the samples (approximately 250 μL) and incubated in the dark at 4°C for 45 min. ..

    Article Title: In mouse and in vitro models, bowel preparation promotes pathogen colonization, translocation, and exacerbation of inflammation.
    Article Snippet: Paraffin was removed from sectioned slides through incubation at 60 ◦ C for 10 min, followed by 2x 10-min incubations in pre-warmed xylenes at 60 ◦ C. Slides were then incubated in 99.5% ethanol for 5 min, then left to dry and circled with a PAP (liquid blocker) pen (Fisher Scientific). .. 108 DAPI (10 μg/mL, Sigma Aldrich), UEA-1 (Fluorescein-labeled Ulex Europaeus Agglutinin I, 40 μg/mL, Vector Laboratories), and WGA (Rhodamine Red-X-labeled Wheat Germ Agglutinin, 30 μg/mL, Vector Laboratories) were applied to fully cover the samples (approximately 250 μL) and incubated in the dark at 4 ◦ C for 45 min. ..



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    Image Search Results


    ( a )Representative images of Epi Ctrl and Epi ΔBmal1 distal colon stained for UEA-1 (violet) and MALII (yellow) to label fucosylated and sialylated mucins, respectively. Shown are samples collected at ZT0 and ZT12, arrowheads indicate mucus thickness. (Scale bar = 20μm). ( b ) UEA-1+ mucus thickness in the distal colon is significantly higher at ZT12 in Epi Ctrl but lower at both times in Epi ΔBmal1 (**p≤0.01). ( c ) MALII+ mucus thickness in the distal colon is significantly higher at ZT12 in Epi Ctrl (*p≤ 0.05), with a significant increase of thickness in Epi ΔBmal1 at ZT0 (*p<0.05). Note, that Epi ΔBmal1 does not show a time-of-day dependent change in MALII. ( d ) UEA-1+ goblet cell area in distal colon crypts s significantly higher at ZT12 in Epi Ctrl (**p≤0.05). While not significantly different from controls, Epi ΔBmal1 do not show this time-of-day change in UEA-1+ mucus thickness. ( e ) MALII+ goblet cell area in distal colon crypts is significantly increased in Epi ΔBmal1 at ZT0 (*p≤0.05).

    Journal: bioRxiv

    Article Title: Epithelial function of the circadian clock gene, Bmal1 , in regulating the mucosa

    doi: 10.64898/2026.04.15.718752

    Figure Lengend Snippet: ( a )Representative images of Epi Ctrl and Epi ΔBmal1 distal colon stained for UEA-1 (violet) and MALII (yellow) to label fucosylated and sialylated mucins, respectively. Shown are samples collected at ZT0 and ZT12, arrowheads indicate mucus thickness. (Scale bar = 20μm). ( b ) UEA-1+ mucus thickness in the distal colon is significantly higher at ZT12 in Epi Ctrl but lower at both times in Epi ΔBmal1 (**p≤0.01). ( c ) MALII+ mucus thickness in the distal colon is significantly higher at ZT12 in Epi Ctrl (*p≤ 0.05), with a significant increase of thickness in Epi ΔBmal1 at ZT0 (*p<0.05). Note, that Epi ΔBmal1 does not show a time-of-day dependent change in MALII. ( d ) UEA-1+ goblet cell area in distal colon crypts s significantly higher at ZT12 in Epi Ctrl (**p≤0.05). While not significantly different from controls, Epi ΔBmal1 do not show this time-of-day change in UEA-1+ mucus thickness. ( e ) MALII+ goblet cell area in distal colon crypts is significantly increased in Epi ΔBmal1 at ZT0 (*p≤0.05).

    Article Snippet: Sections were incubated with biotinylated MAL-II (B-1265-1, Vector Laboratories; 3μg/mL in 1%BSA in PBS) overnight at 4°C, washed in PBS, then incubated with UEA-1 rhodamine (RL-1062-2, Vector Laboratories; 2μg/mL) and streptavidin-FITC (405201, BioLegend; 5μg/mL) in 1% BSA in PBS for 1 hr at room temperature in the dark.

    Techniques: Staining

    Thymic epithelial cell (TEC) subpopulations in the neonatal thymus. A: Representative flow cytometry profiles of CD45 − epithelial cell adhesion molecule (EpCAM) + TECs at postnatal days 1, 3, 5, and 7. B: Total number of TECs in the thymus from the indicated time points. C: Representative flow cytometry profiles of medullary TECs [mTECs; ulex europaeus agglutinin 1 (UEA1) + Ly51 – ] and cortical TECs (cTECs; UEA1 – Ly51 + ) within the CD45 − EpCAM + TEC population from the indicated time points. D: Total number of mTECs ( left panel ) and cTECs ( right panel ) in the thymus from the indicated mice. E: Representative flow cytometry profiles of autoimmune regulator (Aire) expression in mTECs from the indicated time points. F: Frequency ( left panel ) and absolute number ( right panel ) of Aire + mTECs. At least three independent experiments were conducted using neonatal mice. Data are presented as means ± SEM ( B , D , and F ). n = 4 or 5 mice per group ( B , D , and F ). ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, and ∗∗∗∗ P < 0.0001. Max, maximum; NS, not significant.

    Journal: The American Journal of Pathology

    Article Title: Neonatal Thymic Dynamics Influence Autoimmune Pathology by Shaping the Suppressive Potential of Regulatory T Cells

    doi: 10.1016/j.ajpath.2025.12.007

    Figure Lengend Snippet: Thymic epithelial cell (TEC) subpopulations in the neonatal thymus. A: Representative flow cytometry profiles of CD45 − epithelial cell adhesion molecule (EpCAM) + TECs at postnatal days 1, 3, 5, and 7. B: Total number of TECs in the thymus from the indicated time points. C: Representative flow cytometry profiles of medullary TECs [mTECs; ulex europaeus agglutinin 1 (UEA1) + Ly51 – ] and cortical TECs (cTECs; UEA1 – Ly51 + ) within the CD45 − EpCAM + TEC population from the indicated time points. D: Total number of mTECs ( left panel ) and cTECs ( right panel ) in the thymus from the indicated mice. E: Representative flow cytometry profiles of autoimmune regulator (Aire) expression in mTECs from the indicated time points. F: Frequency ( left panel ) and absolute number ( right panel ) of Aire + mTECs. At least three independent experiments were conducted using neonatal mice. Data are presented as means ± SEM ( B , D , and F ). n = 4 or 5 mice per group ( B , D , and F ). ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, and ∗∗∗∗ P < 0.0001. Max, maximum; NS, not significant.

    Article Snippet: Isolated TECs were stained with the following antibodies: BV421-conjugated anti-mouse CD45 (BD Biosciences, Franklin Lakes, NJ; 30-F11); phosphatidylethanolamine-Cy7–conjugated anti-mouse epithelial cell adhesion molecule (BioLegend; G8.8); Alexa Fluor 647–conjugated anti-mouse Ly-51 (BioLegend; 6C3); DyLight 594–conjugated ulex europaeus agglutinin 1 (UEA1) (Vector Laboratories, Newark, CA; DL-1067-1); and Alexa Fluor 488–conjugated anti-mouse Aire (eBioscience; 5H12).

    Techniques: Flow Cytometry, Expressing