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polyclonal rabbit anti phospho mdm2 ser186  (Bioss)


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    Structured Review

    Bioss polyclonal rabbit anti phospho mdm2 ser186
    Polyclonal Rabbit Anti Phospho Mdm2 Ser186, supplied by Bioss, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/polyclonal rabbit anti phospho mdm2 ser186/product/Bioss
    Average 92 stars, based on 4 article reviews
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    92/100 stars

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    Image Search Results


    Journal: bioRxiv

    Article Title: Regulation of the MDM2-p53 Nexus by a Nuclear Phosphoinositide and Small Heat Shock Protein Complex

    doi: 10.1101/2025.04.11.648454

    Figure Lengend Snippet:

    Article Snippet: Monoclonal antibodies against PIP 2 (clone 2C11, #Z-P045, Echelon Biosciences), PIP 2 (clone KT10, #MSBS2283, MilliporeSigma), p53 (clone DO-1, #SC-126, Santa Cruz Biotechnology), HSP27 (clone F-4, #SC-13132, Santa Cruz Biotechnology), αBC (D6S9E, #45844, Cell Signaling), PIPKIIα (PIP4K2A, clone D83C1, #5527, Cell Signaling), PTEN (clone D4,3, #9188, Cell Signaling), GAPDH (clone 0411, #SC-47724, Santa Cruz Biotechnology), and polyclonal antibodies against MDM2 (clone D1V2Z, #86934, Cell Signaling), MDM2 (#AF1244, R&D Systems), αBC (#ab13497, Abcam), PIPKIα (PIP5K1A, #9693, Cell Signaling), PIPKIγ (PIP5K1C, #3296, Cell Signaling), PIPKIIβ (PIP4K2B, #9694, Cell Signaling), PITPNB (#NBP2-19841, Novus Biologicals), FOXO3a (clone 75D8, #2497, Cell Signaling), Histone H2A (#2578, Cell Signaling), Histone H2B (clone D2H6, #12364, Cell Signaling), Ubiquitin (P37, #58395, Cell Signaling) were utilized in this study.

    Techniques: Binding Assay, Fluorescence, Microscale Thermophoresis, Concentration Assay, Incubation, Control, Software, Bacteria

    ( a ) Comparison of relative miR-365-1-5p, miR-99b-3p, miR-193a-5p, miR-125a-3p, miR-690, miR-1195, miR-122-5p, miR-140-3p content between MLO-Y4-sEVs and MC3T3-E1-sEVs by real-time quantitative polymerase chain reaction (qRT-PCR). n=3, Student’s two-sided unpaired t test. ( b ) NSCLC cells were transfected with miR-365a-5p, miR-30c-1-3p, miR-193a-5p, miR-99b-3p mimics, or NC (negative control) in Dulbecco’s modified eagle medium (DMEM). 48 hr later, Cell Counting Kit-8 (CCK-8) assays were performed. n=6, one-way analysis of variance with Turkey’s multiple comparisons test. ( c, d ) NSCLC cells were transfected with miR-99b-3p mimics, NC mimics, miR-99b-3p inhibitor, and NC inhibitor. 48 hr later, EdU flow cytometry were performed. CCK-8 assays were performed at different points in time after transfection. n=6, two-way analysis of variance with Sidak’s multiple comparisons test. ( e ) Schematic diagram of putative miR-99b-3p binding sites in the MDM2 3′-UTR. Green letters denote mutation sites. Relative luciferase activities of wild-type (WT) or mutant (MUT) MDM2 3′-UTRs were determined in A549 cells, which were co-transfected with the miR-99b-3p mimics or negative control. Luciferase activity was normalized using Renilla. n=4, Student’s two-sided unpaired t test. ( f ) MDM2 protein in A549 cells was analyzed by western blot 72 hr after transfection. n=3; one-way analysis of variance with Turkey’s multiple comparisons test. Error bars represent Mean ± SD. No significance (ns) p>0.05, *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001. Figure 3—source data 1. Original table sources for quantification of plots. Figure 3—source data 2. Original western blot images for . Figure 3—source data 3. Original western blot images for with highlighted bands and sample labels.

    Journal: eLife

    Article Title: Mechanically stimulated osteocytes maintain tumor dormancy in bone metastasis of non-small cell lung cancer by releasing small extracellular vesicles

    doi: 10.7554/eLife.89613

    Figure Lengend Snippet: ( a ) Comparison of relative miR-365-1-5p, miR-99b-3p, miR-193a-5p, miR-125a-3p, miR-690, miR-1195, miR-122-5p, miR-140-3p content between MLO-Y4-sEVs and MC3T3-E1-sEVs by real-time quantitative polymerase chain reaction (qRT-PCR). n=3, Student’s two-sided unpaired t test. ( b ) NSCLC cells were transfected with miR-365a-5p, miR-30c-1-3p, miR-193a-5p, miR-99b-3p mimics, or NC (negative control) in Dulbecco’s modified eagle medium (DMEM). 48 hr later, Cell Counting Kit-8 (CCK-8) assays were performed. n=6, one-way analysis of variance with Turkey’s multiple comparisons test. ( c, d ) NSCLC cells were transfected with miR-99b-3p mimics, NC mimics, miR-99b-3p inhibitor, and NC inhibitor. 48 hr later, EdU flow cytometry were performed. CCK-8 assays were performed at different points in time after transfection. n=6, two-way analysis of variance with Sidak’s multiple comparisons test. ( e ) Schematic diagram of putative miR-99b-3p binding sites in the MDM2 3′-UTR. Green letters denote mutation sites. Relative luciferase activities of wild-type (WT) or mutant (MUT) MDM2 3′-UTRs were determined in A549 cells, which were co-transfected with the miR-99b-3p mimics or negative control. Luciferase activity was normalized using Renilla. n=4, Student’s two-sided unpaired t test. ( f ) MDM2 protein in A549 cells was analyzed by western blot 72 hr after transfection. n=3; one-way analysis of variance with Turkey’s multiple comparisons test. Error bars represent Mean ± SD. No significance (ns) p>0.05, *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001. Figure 3—source data 1. Original table sources for quantification of plots. Figure 3—source data 2. Original western blot images for . Figure 3—source data 3. Original western blot images for with highlighted bands and sample labels.

    Article Snippet: Antibody , MDM2 (Rabbit polyclonal) , Proteintech , 66511-1-IG , 1:1000.

    Techniques: Comparison, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Transfection, Negative Control, Modification, Cell Counting, CCK-8 Assay, Flow Cytometry, Binding Assay, Mutagenesis, Luciferase, Activity Assay, Western Blot

    Osteocytes, sensing mechanical stimulation generated by exercise or mechanical loading, inhibit the proliferation and sustain the dormancy of NSCLC cells by releasing small extracellular vesicles (sEVs) with tumor suppressor micro-RNAs (miRNAs), such as miR-99b-3p, which inhibits the proliferation of NSCLC cells by directly targeting murine double minute 2 (MDM2).

    Journal: eLife

    Article Title: Mechanically stimulated osteocytes maintain tumor dormancy in bone metastasis of non-small cell lung cancer by releasing small extracellular vesicles

    doi: 10.7554/eLife.89613

    Figure Lengend Snippet: Osteocytes, sensing mechanical stimulation generated by exercise or mechanical loading, inhibit the proliferation and sustain the dormancy of NSCLC cells by releasing small extracellular vesicles (sEVs) with tumor suppressor micro-RNAs (miRNAs), such as miR-99b-3p, which inhibits the proliferation of NSCLC cells by directly targeting murine double minute 2 (MDM2).

    Article Snippet: Antibody , MDM2 (Rabbit polyclonal) , Proteintech , 66511-1-IG , 1:1000.

    Techniques: Generated

    Journal: eLife

    Article Title: Mechanically stimulated osteocytes maintain tumor dormancy in bone metastasis of non-small cell lung cancer by releasing small extracellular vesicles

    doi: 10.7554/eLife.89613

    Figure Lengend Snippet:

    Article Snippet: Antibody , MDM2 (Rabbit polyclonal) , Proteintech , 66511-1-IG , 1:1000.

    Techniques: Sequencing, In Vitro, Software