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Vector Laboratories
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EY Laboratories
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Biozol Diagnostica Vertrieb GmbH
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BioLynx Inc
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BioNordika Oy
maackia amurensis lectin ii (maa-ii) ![]() Maackia Amurensis Lectin Ii (Maa Ii), supplied by BioNordika Oy, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/maackia+amurensis+lectin+ii/maackia+amurensis+lectin+ii++maa+ii+/pmc06482220-93-9-14 Average 90 stars, based on 1 article reviews
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Funakoshi ltd
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Maackia Amurensis Lectin II (MAL II) Biotinylated is a plant lectin that can be used as a probe to specifically bind biomolecules (such as polysaccharides, peptides, etc.).Maackia Amurensis Lectin II (MAL II) Biotinylated is a
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Maackia amurensis Lectin (MAA/MAL II)-Biotinylated is a plant lectin modified by biotin. Maackia amurensis Lectin (MAA/MAL II)-Biotinylated has the activity to recognize specific sugar structures, specifically the alpha-2, 3-linked sialic acid (HY-I0400). Maackia amurensis Lectin
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Image Search Results
Journal: Frontiers in Pharmacology
Article Title: Mycobacterium tuberculosis infection drives osteoclast overactivation via α2,3-Sialylation to promote pathological bone destruction
doi: 10.3389/fphar.2026.1738896
Figure Lengend Snippet: α2,3-sialylation is required for BCG-induced osteoclast differentiation and activity (A) Comparison of differentially expressed genes (DEGs) between BCG-infected osteoclasts (RB) and uninfected controls (R). (n = 3 biological replicates per group, differential expression was defined as |FoldChange| > 2 and padj <0.05). (B) Volcano plot of DEGs highlighting genes related to sialic acid biosynthesis. (C) KEGG pathway enrichment analysis of upregulated DEGs in RB cells. (D,E) Immunofluorescence staining of α2,3-SA in mouse calvarial sections using MAL II lectin, with quantification of α2,3-SA fluorescence intensity (n = 5). Intensity density was normalized to the PBS group mean. (F) In vitro osteoclasts subjected to MAL II lectin staining and TRAP staining, with or without sialidase treatment to enzymatically remove α2,3-SA. (G) Quantification of α2,3-SA fluorescence intensity in cultured osteoclasts (n = 5). Intensity density was measured in cellular ROIs after background subtraction and normalized to the RANKL group mean. (H) Quantification of TRAP + multinucleated cells (≥3 nuclei) per field (randomly selected fields, fixed magnification) in vitro (n = 5). (I) mRNA expression levels of osteoclast differentiation markers ( Fos, Mmp9, Nfatc1, and Ocstamp ) in osteoclasts (n = 3). Data are presented as mean ± SD. Statistical significance was determined by two-tailed unpaired Student’s t-test for two-group comparisons (E) and one-way ANOVA followed by Tukey’s post hoc test for three-group comparisons (G–I) .
Article Snippet:
Techniques: Activity Assay, Comparison, Infection, Quantitative Proteomics, Immunofluorescence, Staining, Fluorescence, In Vitro, Cell Culture, Expressing, Two Tailed Test
Journal: Frontiers in Microbiology
Article Title: Attachment Patterns of Human and Avian Influenza Viruses to Trachea and Colon of 26 Bird Species – Support for the Community Concept
doi: 10.3389/fmicb.2019.00815
Figure Lengend Snippet: Representative histochemistry images of stained tracheae TMAs. Red color indicates virus/lectin staining. The cells were counterstained with hematoxylin (blue).
Article Snippet: Consecutive TMA sections were stained with either 4 μg/mL
Techniques: Staining, Virus
Journal: Frontiers in Microbiology
Article Title: Attachment Patterns of Human and Avian Influenza Viruses to Trachea and Colon of 26 Bird Species – Support for the Community Concept
doi: 10.3389/fmicb.2019.00815
Figure Lengend Snippet: Representative histochemistry images of stained cola TMAs. Red color indicates virus/lectin staining. The cells were counterstained with hematoxylin (blue).
Article Snippet: Consecutive TMA sections were stained with either 4 μg/mL
Techniques: Staining, Virus