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κ clone 2a3 bio x cell cat bp0089  (Bio X Cell)


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    Structured Review

    Bio X Cell κ clone 2a3 bio x cell cat bp0089
    κ Clone 2a3 Bio X Cell Cat Bp0089, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 96/100, based on 301 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/isotype+control+anti-trinitrophenol+clone+2a3/InVivoPlus+rat+IgG2a+isotype+control%2C+anti-trinitrophenol/pmc13012031-73-25-28
    Average 96 stars, based on 301 article reviews
    κ clone 2a3 bio x cell cat bp0089 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: PD-1/PD-L1 checkpoint blockade harnesses monocyte-derived macrophages to combat cognitive impairment in a tauopathy mouse model
    Article Snippet: .. For PD-1 blockade, PD-1-specific blocking antibody (anti-PD-1; rat IgG2a isotype; clone RPM1-14; BIOXCELL) and isotype control (anti-trinitrophenol; clone 2A3, BIOXCELL) were administered i.p. For PD-L1 blockade, throughout the entire study, PD-L1-blocking antibody directed to mouse PD-L1 was used (anti-PD-L1 antibody; rat IgG2b isotype; clone 10F.9G2; BIOXCELL) and isotype control (anti-keyhole limpet hemocyanin; clone LTF-2; BIOXCELL) was administered i.p. ..

    Control:

    Article Title: PD-1/PD-L1 checkpoint blockade harnesses monocyte-derived macrophages to combat cognitive impairment in a tauopathy mouse model
    Article Snippet: .. For PD-1 blockade, PD-1-specific blocking antibody (anti-PD-1; rat IgG2a isotype; clone RPM1-14; BIOXCELL) and isotype control (anti-trinitrophenol; clone 2A3, BIOXCELL) were administered i.p. For PD-L1 blockade, throughout the entire study, PD-L1-blocking antibody directed to mouse PD-L1 was used (anti-PD-L1 antibody; rat IgG2b isotype; clone 10F.9G2; BIOXCELL) and isotype control (anti-keyhole limpet hemocyanin; clone LTF-2; BIOXCELL) was administered i.p. ..



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    D KO enhances tumor response to antiangiogenic immunotherapy (A) Schematic of the experimental setup. (B) Volume of individual lung tumors (mean ± SEM) in mice treated as indicated and imaged by micro-CT at day 28 post-tumor injection. n=6 D WT mice treated with <t>IgG1+IgG2a</t> (WT IgGs); n=7 D WT mice treated with A2V+α-PD1 (WT A2V+α-PD1); n=5 D KO mice (KO IgGs and KO A2V+α-PD1). Note that each mouse carries several independent lung tumors. Statistical analysis by unpaired Student’s t test performed between control and interventional treatment for each independent genotype. ∗ p ≤ 0.05.
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    D KO enhances tumor response to antiangiogenic immunotherapy (A) Schematic of the experimental setup. (B) Volume of individual lung tumors (mean ± SEM) in mice treated as indicated and imaged by micro-CT at day 28 post-tumor injection. n=6 D WT mice treated with <t>IgG1+IgG2a</t> (WT IgGs); n=7 D WT mice treated with A2V+α-PD1 (WT A2V+α-PD1); n=5 D KO mice (KO IgGs and KO A2V+α-PD1). Note that each mouse carries several independent lung tumors. Statistical analysis by unpaired Student’s t test performed between control and interventional treatment for each independent genotype. ∗ p ≤ 0.05.
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    D KO enhances tumor response to antiangiogenic immunotherapy (A) Schematic of the experimental setup. (B) Volume of individual lung tumors (mean ± SEM) in mice treated as indicated and imaged by micro-CT at day 28 post-tumor injection. n=6 D WT mice treated with <t>IgG1+IgG2a</t> (WT IgGs); n=7 D WT mice treated with A2V+α-PD1 (WT A2V+α-PD1); n=5 D KO mice (KO IgGs and KO A2V+α-PD1). Note that each mouse carries several independent lung tumors. Statistical analysis by unpaired Student’s t test performed between control and interventional treatment for each independent genotype. ∗ p ≤ 0.05.
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    Image Search Results


    D KO enhances tumor response to antiangiogenic immunotherapy (A) Schematic of the experimental setup. (B) Volume of individual lung tumors (mean ± SEM) in mice treated as indicated and imaged by micro-CT at day 28 post-tumor injection. n=6 D WT mice treated with IgG1+IgG2a (WT IgGs); n=7 D WT mice treated with A2V+α-PD1 (WT A2V+α-PD1); n=5 D KO mice (KO IgGs and KO A2V+α-PD1). Note that each mouse carries several independent lung tumors. Statistical analysis by unpaired Student’s t test performed between control and interventional treatment for each independent genotype. ∗ p ≤ 0.05.

    Journal: iScience

    Article Title: Trajectories of macrophage ontogeny and reprogramming in cancer

    doi: 10.1016/j.isci.2025.112498

    Figure Lengend Snippet: D KO enhances tumor response to antiangiogenic immunotherapy (A) Schematic of the experimental setup. (B) Volume of individual lung tumors (mean ± SEM) in mice treated as indicated and imaged by micro-CT at day 28 post-tumor injection. n=6 D WT mice treated with IgG1+IgG2a (WT IgGs); n=7 D WT mice treated with A2V+α-PD1 (WT A2V+α-PD1); n=5 D KO mice (KO IgGs and KO A2V+α-PD1). Note that each mouse carries several independent lung tumors. Statistical analysis by unpaired Student’s t test performed between control and interventional treatment for each independent genotype. ∗ p ≤ 0.05.

    Article Snippet: Rat IgG2a Isotype Control; clone 2A3 , BioXCell , Cat#BE0089 RRID: AB_1107769.

    Techniques: Micro-CT, Injection, Control