biotinylated ulex europaeus agglutinin i (uea i) (Vector Laboratories)
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biotinylated ulex europaeus agglutinin i (uea i)
Biotinylated Ulex Europaeus Agglutinin I (Uea I), supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 519 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ulex+europaeus+agglutinin+uea+i/Biotinylated+Ulex+Europaeus+Agglutinin+I+(UEA+I)/custom%40b-1065%4042537647
Average 96 stars, based on 519 article reviews
Biotinylated Ulex Europaeus Agglutinin I (Uea I), supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 519 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ulex+europaeus+agglutinin+uea+i/Biotinylated+Ulex+Europaeus+Agglutinin+I+(UEA+I)/custom%40b-1065%4042537647
Average 96 stars, based on 519 article reviews
biotinylated ulex europaeus agglutinin i (uea i) - by Bioz Stars,
2026-10
96/100 stars
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Concentration Assay:Article Title: FITC-lectin avidity ofCryptococcus neoformanscell wall and capsular components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans strains.. Cell populations demonstrated marked avidity for terminal a-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Article Title: FITC-Lectin Avidity of Cryptococcus neoformans Cell Wall and Capsular Components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans trains.. Cell populations demonstrated marked avidity for terminal at-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Sterility:Article Title: FITC-lectin avidity ofCryptococcus neoformanscell wall and capsular components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans strains.. Cell populations demonstrated marked avidity for terminal a-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Article Title: FITC-Lectin Avidity of Cryptococcus neoformans Cell Wall and Capsular Components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans trains.. Cell populations demonstrated marked avidity for terminal at-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Incubation:Article Title: FITC-lectin avidity ofCryptococcus neoformanscell wall and capsular components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans strains.. Cell populations demonstrated marked avidity for terminal a-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Article Title: FITC-Lectin Avidity of Cryptococcus neoformans Cell Wall and Capsular Components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans trains.. Cell populations demonstrated marked avidity for terminal at-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Whole Genome Amplification:Article Title: FITC-lectin avidity ofCryptococcus neoformanscell wall and capsular components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans strains.. Cell populations demonstrated marked avidity for terminal a-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. Article Title: FITC-Lectin Avidity of Cryptococcus neoformans Cell Wall and Capsular Components Article Snippet: Flow cytometry and confocal microscopy were used to quantify and visualize FITC-lectin binding to cell-surface carbohydrate ligands of log and stationary phase acapsular and capsular Cryptococcus neoformans trains.. Cell populations demonstrated marked avidity for terminal at-linked mannose and glucose specific FITC-Con A, mannose specific FITCGNL, as well as N-acetylglucosamine specific FITCWGA.. Exposure to other FITC-lectins specific for mannose, fucose and N-acetylgalactosamine resulted in little cell-surface fluorescence. other:Article Title: Pathogenic bacteria and dead cells are internalized by a unique subset of Peyer's patch dendritic cells that express lysozyme. Article Snippet: ACKGROUND & AIMS: Lysozyme has an important ole in preventing bacterial infection.. In the gastrointestinal ract, lysozyme is thought to be mainly expressed by Paneth ells of the crypt epithelium.. We investigated its expression n the Peyer’s patch, a major intestinal site of antigen samling and pathogen entry. |
![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 <t>agglutinin</t> <t>1</t> <t>(UEA1)</t> + 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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_4582/pmc13084582/pmc13084582__gr3.jpg)