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biotinylated plant derived lectin  (Vector Laboratories)


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    Structured Review

    Vector Laboratories biotinylated plant derived lectin
    Biotinylated Plant Derived Lectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 649 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/biotinylated plant derived lectin/product/Vector Laboratories
    Average 96 stars, based on 649 article reviews
    biotinylated plant derived lectin - by Bioz Stars, 2026-03
    96/100 stars

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    CMA activity in PCs correlates with patient survival. ( A ) Representative images of peritumoral areas according to patient classification showing co-localization of puncta pattern expression of LAMP-2A protein (dark brown) with the PC marker α-SMA (pink) in microvessels of GB patients. Samples were classified as severe (highest α-SMA/LAMP-2A co-localization), moderate or mild (basal co-localization) according to the histological evaluation. A1 to A3 shows magnifications of microvessels (v). LAMP-2A co-localizationwith α-SMA + cells is marked with arrows. Scale bar: 100 µm. ( B ) Representative images of PCs marked with <t>PDGFRβ</t> (in red) in microvessels (v) showing co-localization of puncta pattern expression of LAMP-2A protein (in green) in peritumoral areas of severity classified GB patients. B1 to B3 show magnifications of PDGFRβ + cells. Positive co-localization (in yellow) is marked with arrows. Nuclei were stained with DAPI (blue). Scale bar: 100 µm. ( C ) Overall survival shown by Kaplan–Meier curves of the severity classification related to CMA activity in PCs; * p < 0.05: difference between mild and severe; # p < 0.05: difference between mild and moderate. ( D ) Age distribution by gender of the cohort of GB patients; **** p < 0.0001; ns indicates no significance. ( E ) Severity classification related to gender in the age range 30–65 years in the cohort of GB patients; **** p < 0.0001; ns indicates no significance.
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    Image Search Results


    CMA activity in PCs correlates with patient survival. ( A ) Representative images of peritumoral areas according to patient classification showing co-localization of puncta pattern expression of LAMP-2A protein (dark brown) with the PC marker α-SMA (pink) in microvessels of GB patients. Samples were classified as severe (highest α-SMA/LAMP-2A co-localization), moderate or mild (basal co-localization) according to the histological evaluation. A1 to A3 shows magnifications of microvessels (v). LAMP-2A co-localizationwith α-SMA + cells is marked with arrows. Scale bar: 100 µm. ( B ) Representative images of PCs marked with PDGFRβ (in red) in microvessels (v) showing co-localization of puncta pattern expression of LAMP-2A protein (in green) in peritumoral areas of severity classified GB patients. B1 to B3 show magnifications of PDGFRβ + cells. Positive co-localization (in yellow) is marked with arrows. Nuclei were stained with DAPI (blue). Scale bar: 100 µm. ( C ) Overall survival shown by Kaplan–Meier curves of the severity classification related to CMA activity in PCs; * p < 0.05: difference between mild and severe; # p < 0.05: difference between mild and moderate. ( D ) Age distribution by gender of the cohort of GB patients; **** p < 0.0001; ns indicates no significance. ( E ) Severity classification related to gender in the age range 30–65 years in the cohort of GB patients; **** p < 0.0001; ns indicates no significance.

    Journal: International Journal of Molecular Sciences

    Article Title: Expression of Lumican and Osteopontin in Perivascular Areas of the Glioblastoma Peritumoral Niche and Its Value for Prognosis

    doi: 10.3390/ijms26010192

    Figure Lengend Snippet: CMA activity in PCs correlates with patient survival. ( A ) Representative images of peritumoral areas according to patient classification showing co-localization of puncta pattern expression of LAMP-2A protein (dark brown) with the PC marker α-SMA (pink) in microvessels of GB patients. Samples were classified as severe (highest α-SMA/LAMP-2A co-localization), moderate or mild (basal co-localization) according to the histological evaluation. A1 to A3 shows magnifications of microvessels (v). LAMP-2A co-localizationwith α-SMA + cells is marked with arrows. Scale bar: 100 µm. ( B ) Representative images of PCs marked with PDGFRβ (in red) in microvessels (v) showing co-localization of puncta pattern expression of LAMP-2A protein (in green) in peritumoral areas of severity classified GB patients. B1 to B3 show magnifications of PDGFRβ + cells. Positive co-localization (in yellow) is marked with arrows. Nuclei were stained with DAPI (blue). Scale bar: 100 µm. ( C ) Overall survival shown by Kaplan–Meier curves of the severity classification related to CMA activity in PCs; * p < 0.05: difference between mild and severe; # p < 0.05: difference between mild and moderate. ( D ) Age distribution by gender of the cohort of GB patients; **** p < 0.0001; ns indicates no significance. ( E ) Severity classification related to gender in the age range 30–65 years in the cohort of GB patients; **** p < 0.0001; ns indicates no significance.

    Article Snippet: For fluorescent double-labeling of patient’s samples, goat anti-platelet-derived growth factor receptor beta (PDGFRβ; 1/250; BAF1042, R&D Systems, Barcelona, Spain), rabbit anti-LAMP-2A (1/1000; 51-2200, Invitrogen, Waltham, MA, USA) and mouse anti-RGS5 (1/150; MA5-25584, Invitrogen, Waltham, MA, USA) antibodies were used.

    Techniques: Activity Assay, Expressing, Marker, Staining

    Summary of plasma p‐tau immunoassays.

    Journal: Alzheimer's & Dementia

    Article Title: Plasma p‐tau immunoassays in clinical research for Alzheimer's disease

    doi: 10.1002/alz.14397

    Figure Lengend Snippet: Summary of plasma p‐tau immunoassays.

    Article Snippet: , Lilly MSD p‐tau181 assay (Brickman et al., 2021; Ashton et al., 2023) , Eli Lilly , MSD , Biotinylated derivative of the AT270 , SULFO‐TAG‐Ru‐4G10‐E2 which targets an N‐terminal to mid‐region epitope , .

    Techniques: Clinical Proteomics, Binding Assay, Generated, Derivative Assay, Phospho-proteomics