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anti msln polyclonal antibody  (Bioss)


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    Bioss anti msln polyclonal antibody
    Analysis of neutrophils challenged with EVs from MSTO211H spheroids. ( A , B ) Representative plots and histograms from FACS analysis, and bar graphs showing the percentage of positivity of PDL-1 and <t>MSLN,</t> and the mean fluorescence intensity (MFI) of CD66b, CXCR4, and CD62L on the surface of neutrophils incubated for 3 h with EVs isolated from MSTO-211H MCSs ± 72 h of treatment with EPZ-6438. ( C ) Bar graph showing the percentage of proliferating PMA-stimulated T cells after 24 h of incubation with naïve neutrophils or challenge with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs. ( D ) Bar graph showing the number of MSTO-211H MCSs incubated for 24 h with naïve neutrophils or challenged with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs, expressed as the percentage of untreated MCSs. The histograms in ( A – C ), show the means ± SD, ** p ≤ 0.01, *** p ≤ 0.005, **** p ≤ 0.001, ns: not significant.
    Anti Msln Polyclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti msln polyclonal antibody/product/Bioss
    Average 94 stars, based on 2 article reviews
    anti msln polyclonal antibody - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "EZH2 Inhibition in Mesothelioma Cells Increases the Release of Extracellular Vesicles That Skew Neutrophils Toward a Protumor Phenotype"

    Article Title: EZH2 Inhibition in Mesothelioma Cells Increases the Release of Extracellular Vesicles That Skew Neutrophils Toward a Protumor Phenotype

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms262110328

    Analysis of neutrophils challenged with EVs from MSTO211H spheroids. ( A , B ) Representative plots and histograms from FACS analysis, and bar graphs showing the percentage of positivity of PDL-1 and MSLN, and the mean fluorescence intensity (MFI) of CD66b, CXCR4, and CD62L on the surface of neutrophils incubated for 3 h with EVs isolated from MSTO-211H MCSs ± 72 h of treatment with EPZ-6438. ( C ) Bar graph showing the percentage of proliferating PMA-stimulated T cells after 24 h of incubation with naïve neutrophils or challenge with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs. ( D ) Bar graph showing the number of MSTO-211H MCSs incubated for 24 h with naïve neutrophils or challenged with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs, expressed as the percentage of untreated MCSs. The histograms in ( A – C ), show the means ± SD, ** p ≤ 0.01, *** p ≤ 0.005, **** p ≤ 0.001, ns: not significant.
    Figure Legend Snippet: Analysis of neutrophils challenged with EVs from MSTO211H spheroids. ( A , B ) Representative plots and histograms from FACS analysis, and bar graphs showing the percentage of positivity of PDL-1 and MSLN, and the mean fluorescence intensity (MFI) of CD66b, CXCR4, and CD62L on the surface of neutrophils incubated for 3 h with EVs isolated from MSTO-211H MCSs ± 72 h of treatment with EPZ-6438. ( C ) Bar graph showing the percentage of proliferating PMA-stimulated T cells after 24 h of incubation with naïve neutrophils or challenge with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs. ( D ) Bar graph showing the number of MSTO-211H MCSs incubated for 24 h with naïve neutrophils or challenged with EVs from untreated or EPZ-6438-treated MSTO-211H MCSs, expressed as the percentage of untreated MCSs. The histograms in ( A – C ), show the means ± SD, ** p ≤ 0.01, *** p ≤ 0.005, **** p ≤ 0.001, ns: not significant.

    Techniques Used: Fluorescence, Incubation, Isolation



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