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concanavalin a  (InvivoGen)


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    Structured Review

    InvivoGen concanavalin a
    Concanavalin A, supplied by InvivoGen, used in various techniques. Bioz Stars score: 94/100, based on 26 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/concanavalin+a/Concanavalin+A/pmc13390583-61-19-22
    Average 94 stars, based on 26 article reviews
    concanavalin a - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Laser Capture Microdissection:

    Article Title: Pam3CSK4 As a Second Hit in NLRP3‐Dependent Activation of Monocytes Primed With Antiphospholipid Antibodies
    Article Snippet: .. For this, THP‐1 cells were exposed to a panel of following agents: 1 μg/mL peptidoglycan (PGN, Sigma), 10 μg/mL Concanavalin A (ConA, Invivogen), 10 μg/mL polyinosinic:polycytidylic acid (Poly I:C, Sigma), 2.5 μg/mL resiquimod (R848, Invivogen), 100 ng/mL fibroblast‐stimulating lipopeptide (FSL1, Sigma), 100 ng/mL lipopolysaccharide (LPS, Sigma), 5 μg/mL lipoteichoic acid (LTA, Invivogen), 200 ng/mL tripalmitoylated lipopeptide (Pam3CSK4, Invivogen), 10 ng/mL CpG DNA (Invivogen), 100 ng/mL lipoarabinomannan (LAM, Invivogen), 10 μg/mL muramyl dipeptide (MDP, Invivogen), 5 μg/mL single‐stranded RNA40 (ssRNA40, Invivogen), 10 7 cell/mL heat‐killed preparation of Listeria monocytogenes (HKML, Invivogen), and 100 nM N‐Formyl‐Met‐Leu‐Phe (fMLP, Sigma) on the plate with immobilized anti‐β2GPI/β2GPI. .. For this, THP‐1 cells were exposed to a panel of following agents: 1 μg/mL peptidoglycan (PGN, Sigma), 10 μg/mL Concanavalin A (ConA, Invivogen), 10 μg/mL polyinosinic:polycytidylic acid (Poly I:C, Sigma), 2.5 μg/mL resiquimod (R848, Invivogen), 100 ng/mL fibroblast‐stimulating lipopeptide (FSL1, Sigma), 100 ng/mL lipopolysaccharide (LPS, Sigma), 5 μg/mL lipoteichoic acid (LTA, Invivogen), 200 ng/mL tripalmitoylated lipopeptide (Pam3CSK4, Invivogen), 10 ng/mL CpG DNA (Invivogen), 100 ng/mL lipoarabinomannan (LAM, Invivogen), 10 μg/mL muramyl dipeptide (MDP, Invivogen), 5 μg/mL single‐stranded RNA40 (ssRNA40, Invivogen), 10 7 cell/mL heat‐killed preparation of Listeria monocytogenes (HKML, Invivogen), and 100 nM N‐Formyl‐Met‐Leu‐Phe (fMLP, Sigma) on the plate with immobilized anti‐β2GPI/β2GPI.

    Isolation:

    Article Title: IL-12-secreting CAR-T cells reprogram the tumor microenvironment and improve efficacy against heterogeneous models of glioblastoma
    Article Snippet: Retroviral supernatant was produced by co-transfecting HEK 293T cells (ATCC CRL-3216) with the CAR plasmid and pCL-Eco packaging plasmid (Novus Biologicals, #NBP2-29540) using Lipofectamine 2000 (Invitrogen, #11668019). .. Murine splenocytes were isolated from C57BL/6 mice and activated with 2 μg/mL concanavalin A (InvivoGen, #inh-cona-2) and 50 IU/mL recombinant murine IL-2 (PeproTech, #212–12) for 48 hours. .. Murine splenocytes were isolated from C57BL/6 mice and activated with 2 μg/mL concanavalin A (InvivoGen, #inh-cona-2) and 50 IU/mL recombinant murine IL-2 (PeproTech, #212–12) for 48 hours.

    Recombinant:

    Article Title: IL-12-secreting CAR-T cells reprogram the tumor microenvironment and improve efficacy against heterogeneous models of glioblastoma
    Article Snippet: Retroviral supernatant was produced by co-transfecting HEK 293T cells (ATCC CRL-3216) with the CAR plasmid and pCL-Eco packaging plasmid (Novus Biologicals, #NBP2-29540) using Lipofectamine 2000 (Invitrogen, #11668019). .. Murine splenocytes were isolated from C57BL/6 mice and activated with 2 μg/mL concanavalin A (InvivoGen, #inh-cona-2) and 50 IU/mL recombinant murine IL-2 (PeproTech, #212–12) for 48 hours. .. Murine splenocytes were isolated from C57BL/6 mice and activated with 2 μg/mL concanavalin A (InvivoGen, #inh-cona-2) and 50 IU/mL recombinant murine IL-2 (PeproTech, #212–12) for 48 hours.

    Positive Control:

    Article Title: Enhanced Immunogenicity and Dose-Sparing Efficacy of SelfAmplifying RNA Vaccines Against Seasonal Influenza Across Subtypes.
    Article Snippet: .. Unstimulated cells served as negative controls, whereas Concanavalin A (10 μg/mL; InvivoGen, #inh-cona) was used as a positive control. .. GolgiPlugTM (BD Biosciences, #555029) and GolgiStopTM (BD Biosciences, #554724) were added at a 1:1,000 dilution, and the cells were incubated for 6 h at 37°C.

    other:

    Article Title: Enhanced immunogenicity and dose-sparing efficacy of self-amplifying RNA vaccines against seasonal influenza across subtypes
    Article Snippet: The resulting cytokine spots were quantified using an automated ELISpot plate reader (PerkinElmer).



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    Characteristics of in situ <t>biofilm</t> and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Characteristics of in situ <t>biofilm</t> and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    MedChemExpress concanavalin a sigma aldrich
    Characteristics of in situ <t>biofilm</t> and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    InvivoGen concanavalin a
    Characteristics of in situ <t>biofilm</t> and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Image Search Results


    Characteristics of in situ biofilm and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Biofilm

    Article Title: Genomic insights into activated antimicrobial resistance of in situ hospital-wastewater biofilm

    doi: 10.1016/j.bioflm.2026.100377

    Figure Lengend Snippet: Characteristics of in situ biofilm and hospital wastewater samples. ( a ) Placement of plastic slides in hospital wastewater for in situ biofilm formation and collection of wastewater sample. ( b ) In situ biofilm samples before and after crystal-violet staining. ( c ) Fluorescent staining of in situ biofilm structure: green, red, and blue represent nucleic acids, proteins, and polysaccharides, respectively. ( d ) Comparison of contamination levels based on antimicrobial resistance between hospital wastewater and in situ biofilm. Statistical analysis using unpaired t -test; ∗∗∗p < 0.0001. DHL: deoxycholate hydrogen sulfide lactose, CTX: cefotaxime. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: For fluorescence staining, nucleic acid was stained with cell-permeant SYTO 9 (Thermo Fisher Scientific, Waltham, MA, USA), proteins were stained with FilmTracerTM SYPROTM Ruby Biofilm Matrix Stain (Thermo Fisher Scientific), and polysaccharides were stained with Concanavalin A conjugated to tetramethylrhodamine (Thermo Fisher Scientific).

    Techniques: In Situ, Staining, Comparison

    Taxonomic and functional gene profiles of in situ biofilm and hospital wastewater based on shotgun metagenomic data. Relative abundance of bacterial taxa at the order ( a ) and family ( b ) levels in in situ biofilm and hospital wastewater samples. ( c ) Distribution of genes associated with resistance to antibiotics, biocides, acids, heat, and metals, as well as virulence, shown at the metagenome-assembled genome (MAG) and contig levels for biofilm (BF) and hospital wastewater (HW). MLS: macrolide-lincosamide-streptogramin.

    Journal: Biofilm

    Article Title: Genomic insights into activated antimicrobial resistance of in situ hospital-wastewater biofilm

    doi: 10.1016/j.bioflm.2026.100377

    Figure Lengend Snippet: Taxonomic and functional gene profiles of in situ biofilm and hospital wastewater based on shotgun metagenomic data. Relative abundance of bacterial taxa at the order ( a ) and family ( b ) levels in in situ biofilm and hospital wastewater samples. ( c ) Distribution of genes associated with resistance to antibiotics, biocides, acids, heat, and metals, as well as virulence, shown at the metagenome-assembled genome (MAG) and contig levels for biofilm (BF) and hospital wastewater (HW). MLS: macrolide-lincosamide-streptogramin.

    Article Snippet: For fluorescence staining, nucleic acid was stained with cell-permeant SYTO 9 (Thermo Fisher Scientific, Waltham, MA, USA), proteins were stained with FilmTracerTM SYPROTM Ruby Biofilm Matrix Stain (Thermo Fisher Scientific), and polysaccharides were stained with Concanavalin A conjugated to tetramethylrhodamine (Thermo Fisher Scientific).

    Techniques: Functional Assay, In Situ

    Network analysis of metagenome-assembled genomes, functional genes, and mobile genetic elements based on shotgun metagenomic data. Networks of metagenome-assembled genomes (MAGs) and genes related to antimicrobial resistance (AMR), biocide and metal resistance, insertion sequences (ISs), integron, and virulence are depicted for biofilm ( a ) and hospital wastewater ( b ) samples. Nodes represent individual sequences and edges indicate co-occurrence within the same MAG or contig.

    Journal: Biofilm

    Article Title: Genomic insights into activated antimicrobial resistance of in situ hospital-wastewater biofilm

    doi: 10.1016/j.bioflm.2026.100377

    Figure Lengend Snippet: Network analysis of metagenome-assembled genomes, functional genes, and mobile genetic elements based on shotgun metagenomic data. Networks of metagenome-assembled genomes (MAGs) and genes related to antimicrobial resistance (AMR), biocide and metal resistance, insertion sequences (ISs), integron, and virulence are depicted for biofilm ( a ) and hospital wastewater ( b ) samples. Nodes represent individual sequences and edges indicate co-occurrence within the same MAG or contig.

    Article Snippet: For fluorescence staining, nucleic acid was stained with cell-permeant SYTO 9 (Thermo Fisher Scientific, Waltham, MA, USA), proteins were stained with FilmTracerTM SYPROTM Ruby Biofilm Matrix Stain (Thermo Fisher Scientific), and polysaccharides were stained with Concanavalin A conjugated to tetramethylrhodamine (Thermo Fisher Scientific).

    Techniques: Functional Assay

    Differential gene expression profiles between biofilm and hospital wastewater based on metatranscriptomic data. ( a ) Number of genes with higher (Up) or lower (Down) expression in biofilm (BF) compared to hospital wastewater (HW) across all genes. ( b ) Number of genes with significantly different expression (p < 0.05) between BF and HW. ( c ) Volcano plot showing genes with significant expression differences (p < 0.05) between BF and HW, where colors describe functional categories. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Biofilm

    Article Title: Genomic insights into activated antimicrobial resistance of in situ hospital-wastewater biofilm

    doi: 10.1016/j.bioflm.2026.100377

    Figure Lengend Snippet: Differential gene expression profiles between biofilm and hospital wastewater based on metatranscriptomic data. ( a ) Number of genes with higher (Up) or lower (Down) expression in biofilm (BF) compared to hospital wastewater (HW) across all genes. ( b ) Number of genes with significantly different expression (p < 0.05) between BF and HW. ( c ) Volcano plot showing genes with significant expression differences (p < 0.05) between BF and HW, where colors describe functional categories. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: For fluorescence staining, nucleic acid was stained with cell-permeant SYTO 9 (Thermo Fisher Scientific, Waltham, MA, USA), proteins were stained with FilmTracerTM SYPROTM Ruby Biofilm Matrix Stain (Thermo Fisher Scientific), and polysaccharides were stained with Concanavalin A conjugated to tetramethylrhodamine (Thermo Fisher Scientific).

    Techniques: Gene Expression, Expressing, Functional Assay

    Maximum-likelihood phylogenetic tree of Citrobacter species, including isolates from in situ biofilm sample and publicly available genomes. The tree was constructed using core genome sequences and annotated with metadata including sequence type (ST), isolation source, country of origin, and β-lactamase gene profiles.

    Journal: Biofilm

    Article Title: Genomic insights into activated antimicrobial resistance of in situ hospital-wastewater biofilm

    doi: 10.1016/j.bioflm.2026.100377

    Figure Lengend Snippet: Maximum-likelihood phylogenetic tree of Citrobacter species, including isolates from in situ biofilm sample and publicly available genomes. The tree was constructed using core genome sequences and annotated with metadata including sequence type (ST), isolation source, country of origin, and β-lactamase gene profiles.

    Article Snippet: For fluorescence staining, nucleic acid was stained with cell-permeant SYTO 9 (Thermo Fisher Scientific, Waltham, MA, USA), proteins were stained with FilmTracerTM SYPROTM Ruby Biofilm Matrix Stain (Thermo Fisher Scientific), and polysaccharides were stained with Concanavalin A conjugated to tetramethylrhodamine (Thermo Fisher Scientific).

    Techniques: In Situ, Construct, Sequencing, Isolation