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antibody array  (R&D Systems)


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    Structured Review

    R&D Systems antibody array
    Antibody Array, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 25 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+pluripotent+stem+cell+antibody+array/pm39136580-80-2-4?v=R%26D+Systems
    Average 92 stars, based on 25 article reviews
    antibody array - by Bioz Stars, 2026-07
    92/100 stars

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    R&D Systems human pluripotent stem cell antibody array
    FIGURE 1 EVsCSC and EVsDCC isolation and characterization. (A) Representative images of CSCs and DCCs analyzed for tdTomato fluorescence, scale bar = 25 μm. (B) Gene expression of stemness reporters ALDH1A1, Nanog and Oct-4 detected by qPCR for MDA-MB-231 subpopulations. CSC refers to tdTomato + cells cultured in stem cell maintenance media while DCC indicates cells cultured with a minimal presence of CSC (1%-2%) to avoid de-differentiation. CNRQ stands for Calibrated Normalized Relative Quantity with respect to GAPDH and Actin housekeeping genes. (C) 2D laminin invasion assay comparing CSC and DCC cells. (D) CryoTEM imaging of isolated EVsCSC and EVsDCC. (E) Stochastic Optical Resolution Microscopy (STORM) imaging of isolated EVs previously labeled with DiD. (F) Size distribution by nanoparticle tracking analysis (NTA) of EVsCSC and EVsDCC. (G) EVs typical markers, CD81, TSG101 and ALIX and cell lysate control, β-tubulin identified by Western blot. Twenty micrograms of total protein was loaded per lane and cell extracts (CE) were included as controls. (H) ALDH1A1 and CD44 protein cargo in EVCSC and EVsDCC examined by Western blot. (I) Protein cargo of EVCSC and EVsDCC assayed with a Human <t>Pluripotent</t> Stem Cell Array, showing higher content of OCT4, SOX2 and E- Cadherin in EVCSC. In H and I, quantification of blots are shown as the fold change in the band/dot intensity of EVsCSC/EVsDCC. Differences are significant for ALDH1A1, CD44, SOX2 and E-Cadherin (*P < .05)
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    R&D Systems pluripotent stem cell antibody array
    miR-211 overexpression reduced breast cancer stemness in vitro. (A) Around ~200 mg of total protein was extracted from EV and miR-211 transfected breast cancer cell. The experiment was conducted in accordance with the manufacturer’s instructions. Human <t>pluripotent</t> stem cell antibody array <t>(#ARY010)</t> was used to measure the change in the expression profiles of stemness related markers. Representative pictographs showed decreased levels of stem cell markers in miR-211 treatments. (B and C) Validation of differentially expressed stem cells markers in (A) using RT-PCR analysis.
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    FIGURE 1 EVsCSC and EVsDCC isolation and characterization. (A) Representative images of CSCs and DCCs analyzed for tdTomato fluorescence, scale bar = 25 μm. (B) Gene expression of stemness reporters ALDH1A1, Nanog and Oct-4 detected by qPCR for MDA-MB-231 subpopulations. CSC refers to tdTomato + cells cultured in stem cell maintenance media while DCC indicates cells cultured with a minimal presence of CSC (1%-2%) to avoid de-differentiation. CNRQ stands for Calibrated Normalized Relative Quantity with respect to GAPDH and Actin housekeeping genes. (C) 2D laminin invasion assay comparing CSC and DCC cells. (D) CryoTEM imaging of isolated EVsCSC and EVsDCC. (E) Stochastic Optical Resolution Microscopy (STORM) imaging of isolated EVs previously labeled with DiD. (F) Size distribution by nanoparticle tracking analysis (NTA) of EVsCSC and EVsDCC. (G) EVs typical markers, CD81, TSG101 and ALIX and cell lysate control, β-tubulin identified by Western blot. Twenty micrograms of total protein was loaded per lane and cell extracts (CE) were included as controls. (H) ALDH1A1 and CD44 protein cargo in EVCSC and EVsDCC examined by Western blot. (I) Protein cargo of EVCSC and EVsDCC assayed with a Human Pluripotent Stem Cell Array, showing higher content of OCT4, SOX2 and E- Cadherin in EVCSC. In H and I, quantification of blots are shown as the fold change in the band/dot intensity of EVsCSC/EVsDCC. Differences are significant for ALDH1A1, CD44, SOX2 and E-Cadherin (*P < .05)

    Journal: International journal of cancer

    Article Title: Extracellular vesicles secreted by triple-negative breast cancer stem cells trigger premetastatic niche remodeling and metastatic growth in the lungs.

    doi: 10.1002/ijc.34447

    Figure Lengend Snippet: FIGURE 1 EVsCSC and EVsDCC isolation and characterization. (A) Representative images of CSCs and DCCs analyzed for tdTomato fluorescence, scale bar = 25 μm. (B) Gene expression of stemness reporters ALDH1A1, Nanog and Oct-4 detected by qPCR for MDA-MB-231 subpopulations. CSC refers to tdTomato + cells cultured in stem cell maintenance media while DCC indicates cells cultured with a minimal presence of CSC (1%-2%) to avoid de-differentiation. CNRQ stands for Calibrated Normalized Relative Quantity with respect to GAPDH and Actin housekeeping genes. (C) 2D laminin invasion assay comparing CSC and DCC cells. (D) CryoTEM imaging of isolated EVsCSC and EVsDCC. (E) Stochastic Optical Resolution Microscopy (STORM) imaging of isolated EVs previously labeled with DiD. (F) Size distribution by nanoparticle tracking analysis (NTA) of EVsCSC and EVsDCC. (G) EVs typical markers, CD81, TSG101 and ALIX and cell lysate control, β-tubulin identified by Western blot. Twenty micrograms of total protein was loaded per lane and cell extracts (CE) were included as controls. (H) ALDH1A1 and CD44 protein cargo in EVCSC and EVsDCC examined by Western blot. (I) Protein cargo of EVCSC and EVsDCC assayed with a Human Pluripotent Stem Cell Array, showing higher content of OCT4, SOX2 and E- Cadherin in EVCSC. In H and I, quantification of blots are shown as the fold change in the band/dot intensity of EVsCSC/EVsDCC. Differences are significant for ALDH1A1, CD44, SOX2 and E-Cadherin (*P < .05)

    Article Snippet: Human pluripotent stem cell antibody array (R&D Systems, ARY010) was performed in accordance with the manufacturer's instructions.

    Techniques: Isolation, Fluorescence, Gene Expression, Cell Culture, Invasion Assay, Imaging, Microscopy, Labeling, Control, Western Blot

    miR-211 overexpression reduced breast cancer stemness in vitro. (A) Around ~200 mg of total protein was extracted from EV and miR-211 transfected breast cancer cell. The experiment was conducted in accordance with the manufacturer’s instructions. Human pluripotent stem cell antibody array (#ARY010) was used to measure the change in the expression profiles of stemness related markers. Representative pictographs showed decreased levels of stem cell markers in miR-211 treatments. (B and C) Validation of differentially expressed stem cells markers in (A) using RT-PCR analysis.

    Journal: American Journal of Cancer Research

    Article Title: Targeting PDK4 inhibits breast cancer metabolism

    doi:

    Figure Lengend Snippet: miR-211 overexpression reduced breast cancer stemness in vitro. (A) Around ~200 mg of total protein was extracted from EV and miR-211 transfected breast cancer cell. The experiment was conducted in accordance with the manufacturer’s instructions. Human pluripotent stem cell antibody array (#ARY010) was used to measure the change in the expression profiles of stemness related markers. Representative pictographs showed decreased levels of stem cell markers in miR-211 treatments. (B and C) Validation of differentially expressed stem cells markers in (A) using RT-PCR analysis.

    Article Snippet: An apoptosis array (ARY009) detecting the expression level of 35 apoptotic proteins and a human pluripotent stem cell antibody array (ARY010) detecting the relative expression of 15 pluripotent stem cell markers were purchased from R&D Systems (Minneapolis, MN).

    Techniques: Over Expression, In Vitro, Transfection, Ab Array, Expressing, Biomarker Discovery, Reverse Transcription Polymerase Chain Reaction