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cdna membrane (cancer profiling array ii  (Becton Dickinson)

 
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    Becton Dickinson cdna membrane (cancer profiling array ii
    Cdna Membrane (Cancer Profiling Array Ii, supplied by Becton Dickinson, 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/array+membranes/cdna+membrane++cancer+profiling+array+ii/pmc03094717-96-13-22
    Average 90 stars, based on 1 article reviews
    cdna membrane (cancer profiling array ii - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Expressing:

    Article Title: Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancer
    Article Snippet: .. To examine DFNA5 expression in matched human breast normal and tumor tissues, a cDNA membrane (Cancer Profiling Array II) was purchased from BD Biosciences (San Jose, CA), and the protocol was followed according to the manufacturer's recommendation. .. Full-length DFNA5 cDNA was PCR-amplified, gel-purified and radio-labeled using Amersham Megaprime DNA labeling system (GE Healthcare, Piscataway, NJ) and [P 32 ]dCTP (Perkin Elmer, Waltham, MA) according to the user manual.

    Article Title: Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancer
    Article Snippet: .. Cancer profiling array To examine DFNA5 expression in matched human breast normal and tumor tissues, a cDNA membrane (Cancer Profiling Array II) was purchased from BD Biosciences (San Jose, CA), and the protocol was followed according to the manufacturer's recommendation. .. Full-length DFNA5 cDNA was PCR-amplified, gel-purified and radio-labeled using Amersham Megaprime DNA labeling system (GE Healthcare, Piscataway, NJ) and [P 32 ]dCTP (Perkin Elmer, Waltham, MA) according to the user manual.

    Membrane:

    Article Title: Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancer
    Article Snippet: .. To examine DFNA5 expression in matched human breast normal and tumor tissues, a cDNA membrane (Cancer Profiling Array II) was purchased from BD Biosciences (San Jose, CA), and the protocol was followed according to the manufacturer's recommendation. .. Full-length DFNA5 cDNA was PCR-amplified, gel-purified and radio-labeled using Amersham Megaprime DNA labeling system (GE Healthcare, Piscataway, NJ) and [P 32 ]dCTP (Perkin Elmer, Waltham, MA) according to the user manual.

    Article Title: Methylation of the DFNA5 increases risk of lymph node metastasis in human breast cancer
    Article Snippet: .. Cancer profiling array To examine DFNA5 expression in matched human breast normal and tumor tissues, a cDNA membrane (Cancer Profiling Array II) was purchased from BD Biosciences (San Jose, CA), and the protocol was followed according to the manufacturer's recommendation. .. Full-length DFNA5 cDNA was PCR-amplified, gel-purified and radio-labeled using Amersham Megaprime DNA labeling system (GE Healthcare, Piscataway, NJ) and [P 32 ]dCTP (Perkin Elmer, Waltham, MA) according to the user manual.



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    Benzo-17R-RvD2 mimetic in peritonitis limits PMN tissue infiltration and regulates cytokines Mice were administered with vehicle or benzo-17R-RvD2 (1 ng/mouse) together with zymosan A (1 mg/mouse, i.p.) and exudates collected at 4 h. Total leukocytes were enumerated and composition determined by flow cytometry (see B for gating strategy). (A) Exudate PMN numbers; mean ± SEM, n = 4 mice each group, ∗∗ p < 0.01. (B) Proteome analysis was carried out with inflammatory exudates from four individual mice in each group using Proteome Profiler cytokine arrays, which contains 40 cytokines, chemokines, and acute phase proteins. Orthogonal Partial Least Squares Discriminant Analysis (PLS-DA): the score plot (each dot represents the cytokine profile from each mouse) shows clustering among groups (i.e., peritonitis vs. peritonitis plus benzo-17R-RvD2). The loading plot demonstrates correlations in which the measured cytokines contribute to the cluster separation in the score plot. (C) Relative intensities of cytokines, chemokines, and acute phase proteins. Proteome arrays consist of 40 proteins. Among them 18 were present in the peritoneal exudates. Results are mean ± SEM; relative abundance from n = 4 individual mouse exudates, ∗ p < 0.05, ∗∗ p < 0.01; peritonitis plus benzo-17R-RvD2 versus peritonitis alone; Student’s t test.

    Journal: iScience

    Article Title: Nouveau benzo-mimetics of 17R-Resolvin D2 are potent resolution agonists for inflammation

    doi: 10.1016/j.isci.2025.114201

    Figure Lengend Snippet: Benzo-17R-RvD2 mimetic in peritonitis limits PMN tissue infiltration and regulates cytokines Mice were administered with vehicle or benzo-17R-RvD2 (1 ng/mouse) together with zymosan A (1 mg/mouse, i.p.) and exudates collected at 4 h. Total leukocytes were enumerated and composition determined by flow cytometry (see B for gating strategy). (A) Exudate PMN numbers; mean ± SEM, n = 4 mice each group, ∗∗ p < 0.01. (B) Proteome analysis was carried out with inflammatory exudates from four individual mice in each group using Proteome Profiler cytokine arrays, which contains 40 cytokines, chemokines, and acute phase proteins. Orthogonal Partial Least Squares Discriminant Analysis (PLS-DA): the score plot (each dot represents the cytokine profile from each mouse) shows clustering among groups (i.e., peritonitis vs. peritonitis plus benzo-17R-RvD2). The loading plot demonstrates correlations in which the measured cytokines contribute to the cluster separation in the score plot. (C) Relative intensities of cytokines, chemokines, and acute phase proteins. Proteome arrays consist of 40 proteins. Among them 18 were present in the peritoneal exudates. Results are mean ± SEM; relative abundance from n = 4 individual mouse exudates, ∗ p < 0.05, ∗∗ p < 0.01; peritonitis plus benzo-17R-RvD2 versus peritonitis alone; Student’s t test.

    Article Snippet: The supernatant (750 μl) was incubated with the pre-coated Proteome Profiler array membranes (ARY006, R&D Systems) and processed according to the manufacturer’s instructions.

    Techniques: Flow Cytometry