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human ago2 protein  (MedChemExpress)


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    MedChemExpress human ago2 protein
    Human Ago2 Protein, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 90/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+ago2+protein/AGO2%2FArgonaute-2%2C+Human/pmc13130648-35-0-5
    Average 90 stars, based on 4 article reviews
    human ago2 protein - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Transfer of IgG from long COVID patients induces symptomology in mice
    Article Snippet: Human AGO2 protein (Argonaute-2) , MedChemExpress , HY- P72835.



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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) <t>Anti-ago2</t> RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05
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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) <t>Anti-ago2</t> RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05
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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) <t>Anti-ago2</t> RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05
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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) <t>Anti-ago2</t> RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05
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    protein a/g agarose resin bound with human anti- ago2 antibody  (Cell Signaling Technology Inc)
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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) <t>Anti-ago2</t> RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05
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    PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) Anti-ago2 RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05

    Journal: Diabetology & Metabolic Syndrome

    Article Title: Identification of the LncRNA PRNCR1/miR-642a-5p/SSTR3 CeRNA network and its diagnostic value in type 2 diabetes mellitus

    doi: 10.1186/s13098-025-02061-4

    Figure Lengend Snippet: PRNCR1 modulates SSTR3 via sponge adsorption of hsa-miR-642a-5p. ( A ) Results of the cytoplasmic and nuclear PRNCR1 isolation experiment. GADPH is a cytoplasmic location marker, and U6 is a nuclear location marker. ( B ) The binding sites of PRNCR1 or SSTR3 and hsa-miR-642a-5p. ( C ) Verification of the binding of PRNCR1 with hsa-miR-642a-5p via a luciferase assay. ( D ) Verification of the binding of SSTR3 with hsa-miR-642a-5p via a luciferase assay. ( E and F ) Anti-ago2 RIP analysis was performed, followed by qRT-PCR to detect PRNCR1 and hsa-miR-642a-5p. * indicates P < 0.05

    Article Snippet: The cells were lysed with RIPA lysate and incubated with magnetic beads conjugated with human antibody against Ago2 (Proteintech) or normal mouse IgG (Millipore).

    Techniques: Adsorption, Isolation, Marker, Binding Assay, Luciferase, Quantitative RT-PCR