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pframa bio his  (Addgene inc)


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    Structured Review

    Addgene inc pframa bio his
    Pframa Bio His, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/50737/RAMA-bio-His+(Plasmid+%2350737)/pmc12064020-66-18-19
    Average 93 stars, based on 4 article reviews
    pframa bio his - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Recombinant:

    Article Title: Atypical memory B cell frequency correlates with antibody breadth and function in malaria immune adults
    Article Snippet: .. Recombinant extracellular domains of merozoite antigens MSRP5-bio-his (Addgene plasmid #50805), SERA9-bio-his (Addgene plasmid #50820), RAMA-bio-his (Addgene plasmid #50737), and CyRPA-bio-his ( PF D1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright (University of Oxford, Oxford, UK) . .. Plasmids were transiently expressed using the Expi293 Expression System as described previously .

    Article Title: Deposition of complement regulators on the surface of Plasmodium falciparum merozoites depends on the immune status of the host
    Article Snippet: .. Plasmids encoding the recombinant merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-bio-his (Addgene plasmid #50820), PfMSP3-bio (Addgene plasmid #47731), PfRAMA-bio-his (Addgene plasmid #50737), Pf92-bio (Addgene plasmid #47728) and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright, University of Oxford, Oxford, UK [ , ]. .. The plasmids were used for protein expression using the Exp293 expression system (Invitrogen), following manufacturer instructions.

    Article Title: Deposition of complement regulators on the surface of Plasmodium falciparum merozoites depends on the immune status of the host.
    Article Snippet: .. Plasmids encoding the recombinant merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-biohis (Addgene plasmid #50820), PfMSP3-bio (Addgene plasmid #47731), PfRAMA-bio-his (Addgene plasmid #50737), Pf92-bio (Addgene plasmid #47728) and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright, University of Oxford, Oxford, UK [29,30]. .. The plasmids were used for protein expression using the Exp293 expression system (Invitrogen), following manufacturer instructions.

    Article Title: Acquisition and decay of IgM and IgG responses to merozoite antigens after Plasmodium falciparum malaria in Ghanaian children
    Article Snippet: .. Recombinant extracellular domains of merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-bio-his (Addgene plasmid #50820), PfRAMA-bio-his (Addgene plasmid #50737), and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright (University of Oxford, Oxford, UK) [ ]. .. Transient transfection of expression plasmids was performed using the Expi293F TM Expression System Kit (ThermoFisher) as per manufacturer’s instructions.

    Plasmid Preparation:

    Article Title: Atypical memory B cell frequency correlates with antibody breadth and function in malaria immune adults
    Article Snippet: .. Recombinant extracellular domains of merozoite antigens MSRP5-bio-his (Addgene plasmid #50805), SERA9-bio-his (Addgene plasmid #50820), RAMA-bio-his (Addgene plasmid #50737), and CyRPA-bio-his ( PF D1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright (University of Oxford, Oxford, UK) . .. Plasmids were transiently expressed using the Expi293 Expression System as described previously .

    Article Title: Deposition of complement regulators on the surface of Plasmodium falciparum merozoites depends on the immune status of the host
    Article Snippet: .. Plasmids encoding the recombinant merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-bio-his (Addgene plasmid #50820), PfMSP3-bio (Addgene plasmid #47731), PfRAMA-bio-his (Addgene plasmid #50737), Pf92-bio (Addgene plasmid #47728) and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright, University of Oxford, Oxford, UK [ , ]. .. The plasmids were used for protein expression using the Exp293 expression system (Invitrogen), following manufacturer instructions.

    Article Title: Deposition of complement regulators on the surface of Plasmodium falciparum merozoites depends on the immune status of the host.
    Article Snippet: .. Plasmids encoding the recombinant merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-biohis (Addgene plasmid #50820), PfMSP3-bio (Addgene plasmid #47731), PfRAMA-bio-his (Addgene plasmid #50737), Pf92-bio (Addgene plasmid #47728) and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright, University of Oxford, Oxford, UK [29,30]. .. The plasmids were used for protein expression using the Exp293 expression system (Invitrogen), following manufacturer instructions.

    Article Title: Enhancing neutralization of Plasmodium falciparum using a novel monoclonal antibody against the rhoptry-associated membrane antigen
    Article Snippet: .. The plasmid encoding the P. falciparum rhoptry antigen PfRAMA-bio-his (Addgene, plasmid #50737) was a gift from Gavin Wright (Wellcome Sanger Institute, Cambridge, UK). ..

    Article Title: Enhancing neutralization of Plasmodium falciparum using a novel monoclonal antibody against the rhoptry-associated membrane antigen
    Article Snippet: After blocking, PfRAMA was detected by our panel of mouse anti-PfRAMA mAbs (5 μg/mL) and incubated for 1 h. This step was followed by adding a secondary rabbit anti-mouse immunoglobulin—HRP conjugated antibody (DAKO) for 1 h. After washing the membrane, western blots were developed by LumiGLO peroxidase chemiluminescent substrate (SeraCare) and images were acquired using the ChemiDoc MP Imaging System (Bio-rad). .. The gene encoding PfRAMA was amplified from the Addgene plasmid #50737 using Phusion HF PCR Mastermix (NEB) and purified using QIAquick PCR Purification Kit (QIAGEN). .. Next, 5 μg of PCR product was digested with 1 unit of DNaseI (NEB) for 1 min and 45 s. The yielded gene fragments were run on a 1% agarose gel and the smears located between 50 and 250 bp were cut out and purified using QIAX II Gel Extraction Kit (QIAGEN).

    Article Title: Acquisition and decay of IgM and IgG responses to merozoite antigens after Plasmodium falciparum malaria in Ghanaian children
    Article Snippet: .. Recombinant extracellular domains of merozoite antigens PfMSRP5-bio-his (Addgene plasmid #50805), PfSERA9-bio-his (Addgene plasmid #50820), PfRAMA-bio-his (Addgene plasmid #50737), and PfCyRPA-bio-his (PFD1130w-bio-his, Addgene plasmid #50823) were gifts from Dr. Gavin Wright (University of Oxford, Oxford, UK) [ ]. .. Transient transfection of expression plasmids was performed using the Expi293F TM Expression System Kit (ThermoFisher) as per manufacturer’s instructions.

    Amplification:

    Article Title: Enhancing neutralization of Plasmodium falciparum using a novel monoclonal antibody against the rhoptry-associated membrane antigen
    Article Snippet: After blocking, PfRAMA was detected by our panel of mouse anti-PfRAMA mAbs (5 μg/mL) and incubated for 1 h. This step was followed by adding a secondary rabbit anti-mouse immunoglobulin—HRP conjugated antibody (DAKO) for 1 h. After washing the membrane, western blots were developed by LumiGLO peroxidase chemiluminescent substrate (SeraCare) and images were acquired using the ChemiDoc MP Imaging System (Bio-rad). .. The gene encoding PfRAMA was amplified from the Addgene plasmid #50737 using Phusion HF PCR Mastermix (NEB) and purified using QIAquick PCR Purification Kit (QIAGEN). .. Next, 5 μg of PCR product was digested with 1 unit of DNaseI (NEB) for 1 min and 45 s. The yielded gene fragments were run on a 1% agarose gel and the smears located between 50 and 250 bp were cut out and purified using QIAX II Gel Extraction Kit (QIAGEN).

    Polymerase Chain Reaction:

    Article Title: Enhancing neutralization of Plasmodium falciparum using a novel monoclonal antibody against the rhoptry-associated membrane antigen
    Article Snippet: After blocking, PfRAMA was detected by our panel of mouse anti-PfRAMA mAbs (5 μg/mL) and incubated for 1 h. This step was followed by adding a secondary rabbit anti-mouse immunoglobulin—HRP conjugated antibody (DAKO) for 1 h. After washing the membrane, western blots were developed by LumiGLO peroxidase chemiluminescent substrate (SeraCare) and images were acquired using the ChemiDoc MP Imaging System (Bio-rad). .. The gene encoding PfRAMA was amplified from the Addgene plasmid #50737 using Phusion HF PCR Mastermix (NEB) and purified using QIAquick PCR Purification Kit (QIAGEN). .. Next, 5 μg of PCR product was digested with 1 unit of DNaseI (NEB) for 1 min and 45 s. The yielded gene fragments were run on a 1% agarose gel and the smears located between 50 and 250 bp were cut out and purified using QIAX II Gel Extraction Kit (QIAGEN).

    Purification:

    Article Title: Enhancing neutralization of Plasmodium falciparum using a novel monoclonal antibody against the rhoptry-associated membrane antigen
    Article Snippet: After blocking, PfRAMA was detected by our panel of mouse anti-PfRAMA mAbs (5 μg/mL) and incubated for 1 h. This step was followed by adding a secondary rabbit anti-mouse immunoglobulin—HRP conjugated antibody (DAKO) for 1 h. After washing the membrane, western blots were developed by LumiGLO peroxidase chemiluminescent substrate (SeraCare) and images were acquired using the ChemiDoc MP Imaging System (Bio-rad). .. The gene encoding PfRAMA was amplified from the Addgene plasmid #50737 using Phusion HF PCR Mastermix (NEB) and purified using QIAquick PCR Purification Kit (QIAGEN). .. Next, 5 μg of PCR product was digested with 1 unit of DNaseI (NEB) for 1 min and 45 s. The yielded gene fragments were run on a 1% agarose gel and the smears located between 50 and 250 bp were cut out and purified using QIAX II Gel Extraction Kit (QIAGEN).



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    Image Search Results


    DUB-IN-3 inhibits ATC progression by activating ferroptosis. (A-C) The CCK8 assay (A), colony formation assay (B), and transwell assay (C) was applied to present the effect of DUB-IN-3 on the proliferation, colony formation, and migration capability of BHT101 cells. (D) The CCK8 assay was used to assess the responses of BHT101 cells with DUB-IN-3 treatment to RSL-3 ± Fer-1. (E, F) Lipid ROS (E) and GSH (F) levels in DUB-IN-3 treating ATC cells. (G) The parental BHT101 cells were injected into the right underarm of nude mouse, then DUB-IN-3 was intraperitoneally injected every 3 days ( n = 3 mouse per group). The tumors were removed and weighted after 17 days. (H) Representative images of IHC staining for Ki-67. (I) GPR34 stabilized by deubiquitinase USP8 promotes ATC progression via inhibiting ferroptosis. Ns, nonsignificant. p > 0.05, ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001.

    Journal: Mediators of Inflammation

    Article Title: GPR34 Stabilized by Deubiquitinase USP8 Suppresses Ferroptosis of ATC

    doi: 10.1155/mi/5576056

    Figure Lengend Snippet: DUB-IN-3 inhibits ATC progression by activating ferroptosis. (A-C) The CCK8 assay (A), colony formation assay (B), and transwell assay (C) was applied to present the effect of DUB-IN-3 on the proliferation, colony formation, and migration capability of BHT101 cells. (D) The CCK8 assay was used to assess the responses of BHT101 cells with DUB-IN-3 treatment to RSL-3 ± Fer-1. (E, F) Lipid ROS (E) and GSH (F) levels in DUB-IN-3 treating ATC cells. (G) The parental BHT101 cells were injected into the right underarm of nude mouse, then DUB-IN-3 was intraperitoneally injected every 3 days ( n = 3 mouse per group). The tumors were removed and weighted after 17 days. (H) Representative images of IHC staining for Ki-67. (I) GPR34 stabilized by deubiquitinase USP8 promotes ATC progression via inhibiting ferroptosis. Ns, nonsignificant. p > 0.05, ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001.

    Article Snippet: DUB-IN-3 (HY-50737-11866) were obtained from MedChemExpress.

    Techniques: CCK-8 Assay, Colony Assay, Transwell Assay, Migration, Injection, Immunohistochemistry