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dylight 649 conjugated ulex europaeus agglutinin i  (Vector Laboratories)


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    Vector Laboratories dylight 649 conjugated ulex europaeus agglutinin i
    Dylight 649 Conjugated Ulex Europaeus Agglutinin I, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 71 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/DL-1068-1/DyLight+649+labeled+Ulex+Europaeus+Agglutinin+I+(UEA+I)/10__1080_slash_29947448__2026__2654916-45-5-12
    Average 95 stars, based on 71 article reviews
    dylight 649 conjugated ulex europaeus agglutinin i - by Bioz Stars, 2026-11
    95/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: IL-17RA signaling promotes the dedifferentiation of Paneth progenitors through ADAM17 to regenerate gut epithelium post-irradiation.
    Article Snippet: .. Following blocking, tissues were submerged in 1x PBS containing 5% fetal bovine serum with primary anti-bodies against LYZ1FITC (1:200) (Dako: F037201), PCNA (1:200) (Santa Cruz: sc-56), GFP (1:100) (Cell Signaling: 295SS), MUC2 (1:200) (Abcam: ab272692), DCLK1 (1:200) (Cell Signaling: 62257S), ADAM17 (1:200) (Invitrogen: MA5-32572), RFP (1:200) (Rockland: 200-101-379), UEA1-Dylight 649 AR TI CL E IN P RE SS ARTICLE IN PRESS (1:200) (Vector: DL-1068), IL-17RA (1:200) (Abcam: ab180904), ChGA (1:200) (Santa Cruz: sc393941), I-FABP (1:200) (Santa Cruz: sc-374482) and ZO-1 (1:200) (Invitrogen: 61-7300) at 4 C overnight. .. The next day, slides were washed three times with 1x PBS, the sections were incubated for 30 minutes at room temperature with Alexa Fluor® 488 AffiniPureTM Goat Anti-Rabbit IgG (H+L) (1:200) (Jackson ImmunoResearch: 111-545-144), Alexa Fluor® 647 AffiniPureTM F(ab')2 Fragment Goat Anti-Rabbit IgG (H+L)(1:200) (Jackson ImmunoResearch: 111-606-144), Alexa Fluor® 488 AffiniPureTM F(ab')2 Fragment Goat Anti-Mouse IgG (H+L) (1:200) (Jackson ImmunoResearch: 115-546-003), or Alexa Fluor® 647 AffiniPureTM F(ab')2 Fragment Donkey Anti-Goat IgG (H+L) (1:200) (Jackson ImmunoResearch: 705-606-147).

    Article Title: Beyond Histology: A Validated CUBIC-Based Workflow for Volumetric Analysis of Follicles and Cortical Vasculature in Human Ovarian Tissue
    Article Snippet: .. The samples were then incubated in a solution consisting of Ulex Europaeus Agglutinin I (UEA I, DyLight 649, 1:250, DL-1068-1, Vector Laboratories, USA) and nuclear counterstain (DAPI, 1:1000, D1306, Invitrogen, USA) diluted in blocking solution with shaking at 37°C for 3 days. ..

    Incubation:

    Article Title: A 3D microfluidic model of exchange between perfused blood and lymphatic microvascular networks
    Article Snippet: .. For lymphatic visualization, UEA I DyLight 649 (Vector Laboratories, DL-1068-1; 1 : 1000) was added to the lymphatic reservoir and incubated for 1–2 h at 37 °C before perfusion. .. Independent perfusion assays were performed under static hydrostatic pressure heads by loading reservoirs with defined volumes as described below, and live imaging was performed either on a widefield epifluorescence microscope or on a Nikon Ti2-E inverted microscope with an Andor Dragonfly 505 spinning disk confocal system maintained at 37 °C and 5% CO 2 .

    Article Title: Beyond Histology: A Validated CUBIC-Based Workflow for Volumetric Analysis of Follicles and Cortical Vasculature in Human Ovarian Tissue
    Article Snippet: .. The samples were then incubated in a solution consisting of Ulex Europaeus Agglutinin I (UEA I, DyLight 649, 1:250, DL-1068-1, Vector Laboratories, USA) and nuclear counterstain (DAPI, 1:1000, D1306, Invitrogen, USA) diluted in blocking solution with shaking at 37°C for 3 days. ..

    Article Title: A 3D microfluidic model of exchange between perfused blood and lymphatic microvascular networks.
    Article Snippet: .. For lymphatic visualization, UEA I DyLight 649 (Vector Laboratories, DL-1068-1; 1 : 1000) was added to the lymphatic reservoir and incubated for 1–2 h at 37 °C before perfusion. .. Independent perfusion assays were performed under static hydrostatic pressure heads by loading reservoirs with defined volumes as described below, and live imaging was performed either on a widefield epifluorescence microscope or on a Nikon Ti2-E inverted microscope with an Andor Dragonfly 505 spinning disk confocal system maintained at 37 °C and 5% CO2.



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