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elisa ar tic le in pr es s rabbit anti mapk proteintech 14064 1 ap wb  (Proteintech)


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    Structured Review

    Proteintech elisa ar tic le in pr es s rabbit anti mapk proteintech 14064 1 ap wb
    Elisa Ar Tic Le In Pr Es S Rabbit Anti Mapk Proteintech 14064 1 Ap Wb, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1006 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+rabbit+ar/p38+MAPK+Antibody/pm41723529-196-64-74
    Average 96 stars, based on 1006 article reviews
    elisa ar tic le in pr es s rabbit anti mapk proteintech 14064 1 ap wb - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    other:

    Article Title: Exosome-delivered NR2F1-AS1 and NR2F1 drive phenotypic transition from dormancy to proliferation in treatment-resistant prostate cancer via stabilizing hormonal receptors.
    Article Snippet: The principal antibodies listed below were employed: anti-rabbit NR2F1 (24573-1-AP, Proteintech, 1:100), anti-mouse PHB2 (66424-1-Ig, Proteintech, 1:100), anti-rabbit ESR1 (21244-1-AP, Proteintech, 1:100), anti-rabbit AR (22089- 1-AP, Proteintech, 1:100), and anti-mouse HnRNPA2B1 (67445-1-Ig, Proteintech, 1:100).

    Article Title: Exosome-delivered NR2F1-AS1 and NR2F1 drive phenotypic transition from dormancy to proliferation in treatment-resistant prostate cancer via stabilizing hormonal receptors
    Article Snippet: The principal antibodies listed below were employed: anti-rabbit NR2F1 (24573-1-AP, Proteintech, 1:100), anti-mouse PHB2 (66424-1-Ig, Proteintech, 1:100), anti-rabbit ESR1 (21244-1-AP, Proteintech, 1:100), anti-rabbit AR (22089-1-AP, Proteintech, 1:100), and anti-mouse HnRNPA2B1 (67445-1-Ig, Proteintech, 1:100).



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    Image Search Results


    A Bioinformatics prediction of putative AR binding sites (androgen response elements, AREs) in the 5’-promoter region of DRAM1 using the JASPAR database. Dual luciferase assays assessing DRAM1 promoter activity in ( B , C ) A375R and WM793R cells transfected with si-AR or D , E A375 and WM793 cells transfected with AR overexpression. ChIP assays using anti-AR antibody in ( F , G ) AR OE A375 or WM793 cells or H , I AR knockdown A375R and WM793R cells. J Schematic of mutated ARE sequences in the DRAM1 5’-promoter region. Dual luciferase assays in ( K , L ) AR OE A375 and WM793 cells or M , N AR knockdown A375R and WM793R cells transfected with wildtype (WT) or mutant (MT) DRAM1 promoter constructs. Mean ± SEM, n = 3, two-tailed Student’s t test. * p < 0.05; ** p < 0.01; *** p < 0.001; ns no significance.

    Journal: Cell Death & Disease

    Article Title: Androgen receptor-dependent DRAM1 activation drives autophagic resistance to BRAF inhibitors in BRAFV600-mutant melanoma

    doi: 10.1038/s41419-026-08547-x

    Figure Lengend Snippet: A Bioinformatics prediction of putative AR binding sites (androgen response elements, AREs) in the 5’-promoter region of DRAM1 using the JASPAR database. Dual luciferase assays assessing DRAM1 promoter activity in ( B , C ) A375R and WM793R cells transfected with si-AR or D , E A375 and WM793 cells transfected with AR overexpression. ChIP assays using anti-AR antibody in ( F , G ) AR OE A375 or WM793 cells or H , I AR knockdown A375R and WM793R cells. J Schematic of mutated ARE sequences in the DRAM1 5’-promoter region. Dual luciferase assays in ( K , L ) AR OE A375 and WM793 cells or M , N AR knockdown A375R and WM793R cells transfected with wildtype (WT) or mutant (MT) DRAM1 promoter constructs. Mean ± SEM, n = 3, two-tailed Student’s t test. * p < 0.05; ** p < 0.01; *** p < 0.001; ns no significance.

    Article Snippet: Lysates were immunoprecipitated overnight at 4 °C with 5 μg anti-AR (CST, #5153) or IgG control (Proteintech, #30000-0-AP), followed by 3 h incubation with Protein G Magnetic Beads (CST, #9006).

    Techniques: Binding Assay, Luciferase, Activity Assay, Transfection, Over Expression, Knockdown, Mutagenesis, Construct, Two Tailed Test