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rhodamine lens culinaris lectin  (Vector Laboratories)


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    Vector Laboratories rhodamine lens culinaris lectin
    Rhodamine Lens Culinaris Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 139 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/lens+culinaris+lectin/Unconjugated+Lens+Culinaris+Agglutinin+(LCA)/10__1038_slash_s41467___026___71052___4-282-6-10
    Average 93 stars, based on 139 article reviews
    rhodamine lens culinaris lectin - by Bioz Stars, 2026-09
    93/100 stars

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    Whole Genome Amplification:

    Article Title: Enzymatic tailoring of anionic glycans for characterising lectin and antibody specificities in a microarray format.
    Article Snippet: Donor substrates 3'- phosphoadenosine-5'-phosphosulphate (PAPS), cytidine 5′-monophosphate-N-acetyl-- neuraminic acid (CMP-Neu5Ac), cytidine 5′-monophosphate-N-glycolyl--neuraminic acid disodium salt (CMP-Neu5Gc), guanosine 5'-diphospho--L-fucose disodium salt (GDP-Fuc), uridine-5-diphospho-N-acetyl--galactosamine sodium salt (UDP-GalNAc), uridine-5- Jo urn al Pr e-p roo f 10 diphospho--glucuronic acid trisodium salt (UDP-GlcA), uridine-5-diphospho--galactose (UDP-Gal) were purchased from R&D Systems (PAPS), Jennewein Biotechnologie GmbH, Rheinbreitbach, Germany (CMP-Neu5Ac and GDP-Fuc); ChemilyBio (CMP-Neu5Gc) and SigmaAldrich (all others) respectively. .. Lectins and Primary Antibodies Biotinylated lectins concanavalin A (ConA, 5 mg/ml), Erythrina cristagalli lectin (ECL, 5 mg /ml), Griffonia simplicifolia isolectin B4 (GSL-I, 0.5 mg/ml) and II (GSL-II, 2 mg/ml), Lens culinaris lectin (LCA, 5 mg/ml), Maackia amurensis lectin I and II (MAA-I, 2 mg/ml; MAA-II, 1 mg/ml), peanut lectin (PNA 5 mg/ml), Ricinus communis lectin I (RCA, 5 mg/ml), Sambucus nigra/Elderberry Bark lectin (SNA, 2 mg/ml), Vicia villosa lectin (VVA, 2 mg/ml), Wisteria floribunda agglutinin (WFA, 2 mg/ml) and wheat germ agglutinin (WGA, 5 mg/ml), as well as fluorescein labelled soybean lectin (SBA, 2 mg/ml) were purchased from Vector Laboratories, Newark, CA, US. ..



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    https://www.bioz.com/product/lens+culinaris+lectin/Unconjugated+Lens+Culinaris+Agglutinin+(LCA)/10__1038_slash_s41467___026___71052___4-282-6-10
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
    Fluorescein Labeled Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
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    biotinylated lens culinaris agglutinin lca lectin  (Vector Laboratories)
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
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    lens culinaris lectin  (Vector Laboratories)
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    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and <t>lectin</t> (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.
    Lens Culinaris Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 93 stars, based on 1 article reviews
    lens culinaris lectin - by Bioz Stars, 2026-09
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    Image Search Results


    (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and lectin (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.

    Journal: Cell metabolism

    Article Title: Cytoarchitectural multi-depot profiling reveals immune-metabolic crosstalk in human colon-associated adipose tissue

    doi: 10.1016/j.cmet.2025.12.008

    Figure Lengend Snippet: (A) Uniform manifold approximation and projection displaying adipocyte identities and expression densities for main marker genes in the STx data. (B) Dot plots displaying the scaled average expression (expr.) profiles of the top three marker genes for each adipocyte identity in the present work and a previous study. (C) Abundance (abun.) and depot enrichments (scaled proportions, prop.) for the three main adipocyte identities. Significant enrichments ( p < 0.05 using likelihood ratio test, LRT) are indicated. (D) Heatmaps displaying expressional enrichments of Adipo SAA markers across depots. Results are shown as scaled average expression for bulk transcriptomics and proteomics from Krieg et al., as well as STx and snRNA-seq in the main (1) and validation (2) cohorts. (E) Quantification of CES1 and lectin (LCA) normalized mean fluorescence intensity based on tissue sections from six individuals imaged using confocal microscopy. Asterisks denote statistically significant differences (* p < 0.05) comparing depots using one-way repeated measures ANOVA and Tukey’s multiple comparisons test. Error bars are standard error of the mean. (F) Representative image of epiploic WAT stained with LCA and an antibody directed against CES1. Scale bars, 200 μm (merge) and 100 μm (inlay). epi, epiploic; mc, mesocolic; ms, mesenteric; om, omental; sc, subcutaneous.

    Article Snippet: Fluorescein-labeled lectin (1:200, FL-1041, Vector labs) or Dylight649-labeled lectin (1:200, DL-1048–1, Vector labs), together with Hoechst33342 (1:2000, ab228551, Abcam), was applied on the slides for 20 minutes.

    Techniques: Expressing, Marker, Transcriptomics, Biomarker Discovery, Fluorescence, Confocal Microscopy, Staining