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recombinant cd40l protein  (R&D Systems)


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    Structured Review

    R&D Systems recombinant cd40l protein
    Recombinant Cd40l Protein, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+cd40l+protein/Recombinant+Mouse+CD40+Ligand%2FTNFSF5+(HA-tag)+Protein/pm42001092-134-44-47
    Average 94 stars, based on 15 article reviews
    recombinant cd40l protein - by Bioz Stars, 2026-11
    94/100 stars

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    Recombinant:

    Article Title: Actomyosin rings constrain CD40 mobility to organize the dendritic cell immunological synapse.
    Article Snippet: .. Glass coverslips (18 mm, #1.5, Marinefeld) were functionalized by coating them with 100 μg/mL human fibronectin (self-isolated from human sera) and 1 μg/mL CCL21 recombinant protein (Peprotech, 300-35), 10 μg/mL anti-MHCII antibody (Invitrogen, 16-5321-85), ), 10 μg/mL anti-ICAM-1 antibody (eBioscience, 16.0542.81) and 10 μg/mL recombinant CD40L protein (R&D Systems, 8230-CL-050/CF), CD27 (R&D Systems, 574-CD-050), OX40 (R&D Systems, 1256-OX-050), 41BB (R&D Systems, 937-4B-050), GITR (R&D Systems, 524-GR-050), LIGHT (R&D Systems, 1794-LT025/CF) in PBS. ..

    Article Title: Actomyosin rings constrain CD40 mobility to organize the dendritic cell immunological synapse.
    Article Snippet: The recruitment of CD40 to the synapse was quantified using a Nikon Eclipse Ti2-E confocal microscope equipped with a 60X Plan Apo LambdaD immersion oil objective, using 488nm and 640nm excitation lasers. .. Glass coverslips were functionalized with 10 μg/mL anti-MHCII antibody (Invitrogen, 16-5321-85) and 10 μg/mL recombinant CD40L protein (R&D Systems, 8230-CL) as described previously. ..



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    R&D Systems recombinant mouse cd40l
    Epitope-specific priming of CD8+ T cells by B cells and DCs resulted in different activation marker expression profiles. B cells and DCs isolated from the C57Bl/6 spleen were either LPS treated or not and then loaded with SIINFEKL peptide. After 48 h of incubation with CD8+ T cells in the presence or absence of GM-CSF and IL-4, flow cytometry was performed to measure the expression of activation markers ( A ) 4-1BB, ( B ) CD25, ( C ) CD27, ( D ) CD28, ( E ) <t>CD40L,</t> ( F ) FASR, ( G ) CD69, ( H ) Ki67, ( I ) OX40, and ( J ) ICOS. Median fluorescence intensities (MFI) were plotted with mean and standard deviation. The percentage of CD8+ T cells positive for the expression of the respective cell surface markers are shown in . Each treatment group was tested with five biological replicates and each data point on the plot represents a biological replicate. Asterisks * indicate p < 0.05, ** indicates p < 0.01, *** indicates p < 0.001, and **** indicates p < 0.0001. Results are representative of at least two similar, independent experiments.
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    ACROBiosystems recombinant human cd40l
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    Epitope-specific priming of CD8+ T cells by B cells and DCs resulted in different activation marker expression profiles. B cells and DCs isolated from the C57Bl/6 spleen were either LPS treated or not and then loaded with SIINFEKL peptide. After 48 h of incubation with CD8+ T cells in the presence or absence of GM-CSF and IL-4, flow cytometry was performed to measure the expression of activation markers ( A ) 4-1BB, ( B ) CD25, ( C ) CD27, ( D ) CD28, ( E ) CD40L, ( F ) FASR, ( G ) CD69, ( H ) Ki67, ( I ) OX40, and ( J ) ICOS. Median fluorescence intensities (MFI) were plotted with mean and standard deviation. The percentage of CD8+ T cells positive for the expression of the respective cell surface markers are shown in . Each treatment group was tested with five biological replicates and each data point on the plot represents a biological replicate. Asterisks * indicate p < 0.05, ** indicates p < 0.01, *** indicates p < 0.001, and **** indicates p < 0.0001. Results are representative of at least two similar, independent experiments.

    Journal: Vaccines

    Article Title: CD8+ T Cells Primed by Antigenic Peptide-Pulsed B Cells or Dendritic Cells Generate Similar Anti-Tumor Response

    doi: 10.3390/vaccines13090953

    Figure Lengend Snippet: Epitope-specific priming of CD8+ T cells by B cells and DCs resulted in different activation marker expression profiles. B cells and DCs isolated from the C57Bl/6 spleen were either LPS treated or not and then loaded with SIINFEKL peptide. After 48 h of incubation with CD8+ T cells in the presence or absence of GM-CSF and IL-4, flow cytometry was performed to measure the expression of activation markers ( A ) 4-1BB, ( B ) CD25, ( C ) CD27, ( D ) CD28, ( E ) CD40L, ( F ) FASR, ( G ) CD69, ( H ) Ki67, ( I ) OX40, and ( J ) ICOS. Median fluorescence intensities (MFI) were plotted with mean and standard deviation. The percentage of CD8+ T cells positive for the expression of the respective cell surface markers are shown in . Each treatment group was tested with five biological replicates and each data point on the plot represents a biological replicate. Asterisks * indicate p < 0.05, ** indicates p < 0.01, *** indicates p < 0.001, and **** indicates p < 0.0001. Results are representative of at least two similar, independent experiments.

    Article Snippet: Recombinant mouse CD40L (Cat.# 8230-CL-050/CF) was purchased from R&D systems (Minneapolis, MN, USA).

    Techniques: Activation Assay, Marker, Expressing, Isolation, Incubation, Flow Cytometry, Fluorescence, Standard Deviation