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anti uea1 biotin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories anti uea1 biotin
    Anti Uea1 Biotin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 10005 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/uea1+biotin/Streptavidin/pm39959339-44-30-31
    Average 99 stars, based on 10005 article reviews
    anti uea1 biotin - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Staining:

    Article Title: The alarmin IL33 orchestrates type 2 immune-mediated control of thymus regeneration
    Article Snippet: Lineage panel used for ILC analysis was anti-CD3ε clone 145-2C11, PE Cy7 (1:200), Biolegend, anti-CD5 clone 53-7.3, PE Cy7 (1:200), eBioscience, anti-CD11b clone ICRF44, PE Cy7 (1:200), Invitrogen, anti-CD11c clone N418, PE Cy7 (1:200), Invitrogen, and anti-B220 clone RA3-6B2, PE Cy7 (1:200), Invitrogen. .. For TEC, mesenchyme, and endothelial analysis , , thymus tissues were digested with collagenase dispase (2.5 mg/ml) (Roche) and DNase I (100 mg/ml) (Roche) before being stained with the following antibodies/reagents: anti-EpCAM1 clone G8.8, Brilliant Violet 711 (1:400), PerCP-eFluor 710 (1:2000), eBioscience, UEA1 Biotin (1:10000) (Vector Labs) detected using streptavidin PE Cy7 (1:1500), eBioscience, anti-Ly51 clone BP-1, PerCP-eFluor 710 (1:600), BD Pharmingen, anti-MHCII clone M5/114.15.2, Alexa Fluor 700 (1:1200), eBioscience, anti-CD80 clone 16-10A1, Brilliant Violet 605 (1:400), BioLegend, anti-CD31 clone 390, PE Cy7 (1:800), Invitrogen, anti-Sca-1 clone D7, PE (1:2000), FITC (1:1000), eBioscience, anti-IL4Ra clone I015F8, PE (1:50), BioLegend, anti-Integrinα7 clone 334908, Alexa Fluor 700 (1:100), R&D, and Zombie Aqua Fixable Viability Kit, Brilliant Violet 510 (1:1000), BioLegend. .. All flow cytometric data were collected on a BD LSR Fortessa running FACs DIVA (v.9.0) and analysed using FlowJo version v10.8.1.

    Article Title: Essential role of IkappaB kinase alpha in thymic organogenesis required for the establishment of self-tolerance.
    Article Snippet: .. Briefly, frozen tissue sections were fixed in cold acetone and stained by first incubating them with ER-TR5 (27) and UEA1-biotin (Vector Laboratories). .. After being washed, the sections were further incubated with Alexa 594-conjugated goat anti-rat IgG (Invitrogen Life Technologies) and Alexa 488-conjugated streptavidin (Invitrogen Life Technologies) for the immunofluorescence.

    Article Title: The transcription factor Sox4 is required for thymic tuft cell development.
    Article Snippet: Medullary thymic epithelial cells (mTECs) help shape the thymic microenvironment for T-cell development by expressing a variety of peripheral tissue-restricted antigens (TRAs).. The selftolerance of T cells is established by negative selection of autoreactive T cells that bind to TRAs.. To increase the diversity of TRAs, a fraction of mTECs terminally differentiates into distinct subsets resembling atypical types of epithelial cells in specific peripheral tissues.

    Flow Cytometry:

    Article Title: Fine-tuning of β-catenin in mouse thymic epithelial cells is required for postnatal T-cell development
    Article Snippet: Antibody , Anti-Ly51-PE(Rat monoclonal, clone 6C3) , BioLegend , Cat# 108308, RRID: AB_313365 , FC (1:100). .. Antibody , Ulex Europaeus Agglutinin I (UEA1)-Biotin , Vector Laboratories , Cat# B-1065, RRID: AB_2336766 , FC (1:1000). .. Antibody , Ulex Europaeus Agglutinin I (UEA1)-DyLight 649 , Vector Laboratories , Cat# DL-1068 , FC (1:500).

    Immunohistochemical staining:

    Article Title: The transcription factor Sox4 is required for thymic tuft cell development.
    Article Snippet: Medullary thymic epithelial cells (mTECs) help shape the thymic microenvironment for T-cell development by expressing a variety of peripheral tissue-restricted antigens (TRAs).. The selftolerance of T cells is established by negative selection of autoreactive T cells that bind to TRAs.. To increase the diversity of TRAs, a fraction of mTECs terminally differentiates into distinct subsets resembling atypical types of epithelial cells in specific peripheral tissues.



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    Vector Laboratories uea1 biotin
    a Representative FACs plots illustrating the proportion of IL33 cit expressing CD45 + thymic cells and total CD45 - thymic stromal cells (blue histogram). Red histograms represent florescence levels in control WT mice. b Quantitation of IL33 cit expression in defined thymic stromal populations; cTEC (CD45 - EpCAM-1 − <t>UEA1</t> − Ly51 + ), mTEC (CD45 - EpCAM-1 − UEA1 + Ly51 − ), mTEC hi (CD45 - EpCAM-1 − UEA1 + Ly51 − MHCII + CD80 + ), mTEC lo (CD45 - EpCAM-1 - UEA1 + Ly51 − MHCII - CD80 − ), Endothelium (TER119 − CD45 − EpCAM-1 − CD31 + ), Mesenchyme (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 − ), Pericytes (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 + ), (where n = 7 animals for TEC subsets and n = 5 animals for all other subsets, obtained from 2 independent experiments). c Representative FACs plots showing Sca-1 expression in thymic mesenchyme, and IL33 cit expression within Sca-1 + and Sca-1 − subsets. Blue histograms are from IL33 cit mice, red histograms from control WT mice. d Total thymus cellularity, Sca-1 + mesenchyme numbers/proportions in WT mice following SLI exposure at indicated time points ( n = 6 animals obtained from 2 independent experiments) with statistical analysis from a one-way ANOVA comparing means of each group to D0 with Dunnett’s multiple comparisons. e Comparative analysis of TEC (blue line) and Sca-1 + mesenchyme (red line) recovery at indicated time points in WT mice ( n = 6 animals obtained from 2 independent experiments). f FACs plots showing IL4Rα expression in Sca-1 + mesenchyme from WT (blue histogram) mice, where against Il4ra −/− mice (red histogram) were used for control staining levels. g Quantitation of Sca1 + mesenchyme in WT and Il4ra −/− mice at steady state (D0) (WT n = 5 and Il4ra −/− n = 6 animals obtained from 2 independent experiments), from a two-tailed unpaired Student’s t test. h Injection and irradiation regime of 5μg recombinant IL4-complexes/PBS into WT mice. Analysis of Sca-1 + mesenchyme was performed at day 7 and day 14 after injection regime, n = 6 minimum. i Numbers of Sca-1 + thymic mesenchyme cells at day 7 and day 14 post-SLI following PBS (D7 n = 6 and D14 n = 7 animals) or IL4c (D7 n = 7 and D14 n = 7 animals) injection, obtained from 2 independent experiments. Statistics from a two-tailed unpaired Student’s t test. All analysis was carried out across at least two independent experiments. All error bars show mean ± SEM.
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    a Representative FACs plots illustrating the proportion of IL33 cit expressing CD45 + thymic cells and total CD45 - thymic stromal cells (blue histogram). Red histograms represent florescence levels in control WT mice. b Quantitation of IL33 cit expression in defined thymic stromal populations; cTEC (CD45 - EpCAM-1 − <t>UEA1</t> − Ly51 + ), mTEC (CD45 - EpCAM-1 − UEA1 + Ly51 − ), mTEC hi (CD45 - EpCAM-1 − UEA1 + Ly51 − MHCII + CD80 + ), mTEC lo (CD45 - EpCAM-1 - UEA1 + Ly51 − MHCII - CD80 − ), Endothelium (TER119 − CD45 − EpCAM-1 − CD31 + ), Mesenchyme (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 − ), Pericytes (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 + ), (where n = 7 animals for TEC subsets and n = 5 animals for all other subsets, obtained from 2 independent experiments). c Representative FACs plots showing Sca-1 expression in thymic mesenchyme, and IL33 cit expression within Sca-1 + and Sca-1 − subsets. Blue histograms are from IL33 cit mice, red histograms from control WT mice. d Total thymus cellularity, Sca-1 + mesenchyme numbers/proportions in WT mice following SLI exposure at indicated time points ( n = 6 animals obtained from 2 independent experiments) with statistical analysis from a one-way ANOVA comparing means of each group to D0 with Dunnett’s multiple comparisons. e Comparative analysis of TEC (blue line) and Sca-1 + mesenchyme (red line) recovery at indicated time points in WT mice ( n = 6 animals obtained from 2 independent experiments). f FACs plots showing IL4Rα expression in Sca-1 + mesenchyme from WT (blue histogram) mice, where against Il4ra −/− mice (red histogram) were used for control staining levels. g Quantitation of Sca1 + mesenchyme in WT and Il4ra −/− mice at steady state (D0) (WT n = 5 and Il4ra −/− n = 6 animals obtained from 2 independent experiments), from a two-tailed unpaired Student’s t test. h Injection and irradiation regime of 5μg recombinant IL4-complexes/PBS into WT mice. Analysis of Sca-1 + mesenchyme was performed at day 7 and day 14 after injection regime, n = 6 minimum. i Numbers of Sca-1 + thymic mesenchyme cells at day 7 and day 14 post-SLI following PBS (D7 n = 6 and D14 n = 7 animals) or IL4c (D7 n = 7 and D14 n = 7 animals) injection, obtained from 2 independent experiments. Statistics from a two-tailed unpaired Student’s t test. All analysis was carried out across at least two independent experiments. All error bars show mean ± SEM.
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    Image Search Results


    a Representative FACs plots illustrating the proportion of IL33 cit expressing CD45 + thymic cells and total CD45 - thymic stromal cells (blue histogram). Red histograms represent florescence levels in control WT mice. b Quantitation of IL33 cit expression in defined thymic stromal populations; cTEC (CD45 - EpCAM-1 − UEA1 − Ly51 + ), mTEC (CD45 - EpCAM-1 − UEA1 + Ly51 − ), mTEC hi (CD45 - EpCAM-1 − UEA1 + Ly51 − MHCII + CD80 + ), mTEC lo (CD45 - EpCAM-1 - UEA1 + Ly51 − MHCII - CD80 − ), Endothelium (TER119 − CD45 − EpCAM-1 − CD31 + ), Mesenchyme (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 − ), Pericytes (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 + ), (where n = 7 animals for TEC subsets and n = 5 animals for all other subsets, obtained from 2 independent experiments). c Representative FACs plots showing Sca-1 expression in thymic mesenchyme, and IL33 cit expression within Sca-1 + and Sca-1 − subsets. Blue histograms are from IL33 cit mice, red histograms from control WT mice. d Total thymus cellularity, Sca-1 + mesenchyme numbers/proportions in WT mice following SLI exposure at indicated time points ( n = 6 animals obtained from 2 independent experiments) with statistical analysis from a one-way ANOVA comparing means of each group to D0 with Dunnett’s multiple comparisons. e Comparative analysis of TEC (blue line) and Sca-1 + mesenchyme (red line) recovery at indicated time points in WT mice ( n = 6 animals obtained from 2 independent experiments). f FACs plots showing IL4Rα expression in Sca-1 + mesenchyme from WT (blue histogram) mice, where against Il4ra −/− mice (red histogram) were used for control staining levels. g Quantitation of Sca1 + mesenchyme in WT and Il4ra −/− mice at steady state (D0) (WT n = 5 and Il4ra −/− n = 6 animals obtained from 2 independent experiments), from a two-tailed unpaired Student’s t test. h Injection and irradiation regime of 5μg recombinant IL4-complexes/PBS into WT mice. Analysis of Sca-1 + mesenchyme was performed at day 7 and day 14 after injection regime, n = 6 minimum. i Numbers of Sca-1 + thymic mesenchyme cells at day 7 and day 14 post-SLI following PBS (D7 n = 6 and D14 n = 7 animals) or IL4c (D7 n = 7 and D14 n = 7 animals) injection, obtained from 2 independent experiments. Statistics from a two-tailed unpaired Student’s t test. All analysis was carried out across at least two independent experiments. All error bars show mean ± SEM.

    Journal: Nature Communications

    Article Title: The alarmin IL33 orchestrates type 2 immune-mediated control of thymus regeneration

    doi: 10.1038/s41467-023-43072-x

    Figure Lengend Snippet: a Representative FACs plots illustrating the proportion of IL33 cit expressing CD45 + thymic cells and total CD45 - thymic stromal cells (blue histogram). Red histograms represent florescence levels in control WT mice. b Quantitation of IL33 cit expression in defined thymic stromal populations; cTEC (CD45 - EpCAM-1 − UEA1 − Ly51 + ), mTEC (CD45 - EpCAM-1 − UEA1 + Ly51 − ), mTEC hi (CD45 - EpCAM-1 − UEA1 + Ly51 − MHCII + CD80 + ), mTEC lo (CD45 - EpCAM-1 - UEA1 + Ly51 − MHCII - CD80 − ), Endothelium (TER119 − CD45 − EpCAM-1 − CD31 + ), Mesenchyme (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 − ), Pericytes (TER119 − CD45 − EpCAM-1 − CD31 − Integrinα7 + ), (where n = 7 animals for TEC subsets and n = 5 animals for all other subsets, obtained from 2 independent experiments). c Representative FACs plots showing Sca-1 expression in thymic mesenchyme, and IL33 cit expression within Sca-1 + and Sca-1 − subsets. Blue histograms are from IL33 cit mice, red histograms from control WT mice. d Total thymus cellularity, Sca-1 + mesenchyme numbers/proportions in WT mice following SLI exposure at indicated time points ( n = 6 animals obtained from 2 independent experiments) with statistical analysis from a one-way ANOVA comparing means of each group to D0 with Dunnett’s multiple comparisons. e Comparative analysis of TEC (blue line) and Sca-1 + mesenchyme (red line) recovery at indicated time points in WT mice ( n = 6 animals obtained from 2 independent experiments). f FACs plots showing IL4Rα expression in Sca-1 + mesenchyme from WT (blue histogram) mice, where against Il4ra −/− mice (red histogram) were used for control staining levels. g Quantitation of Sca1 + mesenchyme in WT and Il4ra −/− mice at steady state (D0) (WT n = 5 and Il4ra −/− n = 6 animals obtained from 2 independent experiments), from a two-tailed unpaired Student’s t test. h Injection and irradiation regime of 5μg recombinant IL4-complexes/PBS into WT mice. Analysis of Sca-1 + mesenchyme was performed at day 7 and day 14 after injection regime, n = 6 minimum. i Numbers of Sca-1 + thymic mesenchyme cells at day 7 and day 14 post-SLI following PBS (D7 n = 6 and D14 n = 7 animals) or IL4c (D7 n = 7 and D14 n = 7 animals) injection, obtained from 2 independent experiments. Statistics from a two-tailed unpaired Student’s t test. All analysis was carried out across at least two independent experiments. All error bars show mean ± SEM.

    Article Snippet: For TEC, mesenchyme, and endothelial analysis , , thymus tissues were digested with collagenase dispase (2.5 mg/ml) (Roche) and DNase I (100 mg/ml) (Roche) before being stained with the following antibodies/reagents: anti-EpCAM1 clone G8.8, Brilliant Violet 711 (1:400), PerCP-eFluor 710 (1:2000), eBioscience, UEA1 Biotin (1:10000) (Vector Labs) detected using streptavidin PE Cy7 (1:1500), eBioscience, anti-Ly51 clone BP-1, PerCP-eFluor 710 (1:600), BD Pharmingen, anti-MHCII clone M5/114.15.2, Alexa Fluor 700 (1:1200), eBioscience, anti-CD80 clone 16-10A1, Brilliant Violet 605 (1:400), BioLegend, anti-CD31 clone 390, PE Cy7 (1:800), Invitrogen, anti-Sca-1 clone D7, PE (1:2000), FITC (1:1000), eBioscience, anti-IL4Ra clone I015F8, PE (1:50), BioLegend, anti-Integrinα7 clone 334908, Alexa Fluor 700 (1:100), R&D, and Zombie Aqua Fixable Viability Kit, Brilliant Violet 510 (1:1000), BioLegend.

    Techniques: Expressing, Quantitation Assay, Staining, Two Tailed Test, Injection, Irradiation, Recombinant