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rabbit anti-mouse thy-1 polyclonal antibody  (Yanke Inc)

 
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    Yanke Inc rabbit anti-mouse thy-1 polyclonal antibody
    Rabbit Anti Mouse Thy 1 Polyclonal Antibody, supplied by Yanke Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti-mouse+thy-1+polyclonal+antibody/pm31753724-83-43-53?v=Yanke+Inc
    Average 90 stars, based on 1 article reviews
    rabbit anti-mouse thy-1 polyclonal antibody - by Bioz Stars, 2026-07
    90/100 stars

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    Factor XII-W268R displays spontaneous activity during protein expression.
A, Western blotting of expression medium under reducing (R) conditions. The closed arrow indicates the FXIIa light chain. The image is representative of three separate experiments. B, chromogenic substrate assay for FXIIa activity in expression medium. C, quantification of FXIIa activity in expression medium. Substrate conversion (linear) was monitored in the first 20 min of the assays and fitted to a standard curve of αFXIIa in expression medium. D, chromogenic substrate assay for plasma prekallikrein activator activity in expression medium. E, effects of PPACK, C1-INH, or antibody OT2 on FXIIa activity in expression medium. F, FXIIa–C1-INH complex formation in expression medium. After incubation with C1-INH, a sigmoidal 4PL fit model was used to interpolate concentrations from a standard curve. The figure panels represent means and S.D. of three repeated experiments.
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    Factor XII-W268R displays spontaneous activity during protein expression.
A, Western blotting of expression medium under reducing (R) conditions. The closed arrow indicates the FXIIa light chain. The image is representative of three separate experiments. B, chromogenic substrate assay for FXIIa activity in expression medium. C, quantification of FXIIa activity in expression medium. Substrate conversion (linear) was monitored in the first 20 min of the assays and fitted to a standard curve of αFXIIa in expression medium. D, chromogenic substrate assay for plasma prekallikrein activator activity in expression medium. E, effects of PPACK, C1-INH, or antibody OT2 on FXIIa activity in expression medium. F, FXIIa–C1-INH complex formation in expression medium. After incubation with C1-INH, a sigmoidal 4PL fit model was used to interpolate concentrations from a standard curve. The figure panels represent means and S.D. of three repeated experiments.
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    Factor XII-W268R displays spontaneous activity during protein expression.
A, Western blotting of expression medium under reducing (R) conditions. The closed arrow indicates the FXIIa light chain. The image is representative of three separate experiments. B, chromogenic substrate assay for FXIIa activity in expression medium. C, quantification of FXIIa activity in expression medium. Substrate conversion (linear) was monitored in the first 20 min of the assays and fitted to a standard curve of αFXIIa in expression medium. D, chromogenic substrate assay for plasma prekallikrein activator activity in expression medium. E, effects of PPACK, C1-INH, or antibody OT2 on FXIIa activity in expression medium. F, FXIIa–C1-INH complex formation in expression medium. After incubation with C1-INH, a sigmoidal 4PL fit model was used to interpolate concentrations from a standard curve. The figure panels represent means and S.D. of three repeated experiments.
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    Image Search Results


    Identification of surface biomarkers of BM-MSCs. Flow cytometry of (A) CD90 and (B) CD34. (C) Immunocytochemical staining for expression of CD90 of BM-MSCs. Magnification, ×200. BM-MSCs, bone marrow-derived mesenchymal stem cells.

    Journal: Molecular Medicine Reports

    Article Title: Yi Guan Jian decoction may enhance hepatic differentiation of bone marrow-derived mesenchymal stem cells via SDF-1 in vitro

    doi: 10.3892/mmr.2017.6888

    Figure Lengend Snippet: Identification of surface biomarkers of BM-MSCs. Flow cytometry of (A) CD90 and (B) CD34. (C) Immunocytochemical staining for expression of CD90 of BM-MSCs. Magnification, ×200. BM-MSCs, bone marrow-derived mesenchymal stem cells.

    Article Snippet: The cells were then incubated with the primary antibody rabbit anti-mouse CD90 (1:200; cat no. bs-0778R; BIOSS, Beijing, China) at 4°C overnight.

    Techniques: Flow Cytometry, Staining, Expressing, Derivative Assay

    Factor XII-W268R displays spontaneous activity during protein expression.
A, Western blotting of expression medium under reducing (R) conditions. The closed arrow indicates the FXIIa light chain. The image is representative of three separate experiments. B, chromogenic substrate assay for FXIIa activity in expression medium. C, quantification of FXIIa activity in expression medium. Substrate conversion (linear) was monitored in the first 20 min of the assays and fitted to a standard curve of αFXIIa in expression medium. D, chromogenic substrate assay for plasma prekallikrein activator activity in expression medium. E, effects of PPACK, C1-INH, or antibody OT2 on FXIIa activity in expression medium. F, FXIIa–C1-INH complex formation in expression medium. After incubation with C1-INH, a sigmoidal 4PL fit model was used to interpolate concentrations from a standard curve. The figure panels represent means and S.D. of three repeated experiments.

    Journal: The Journal of Biological Chemistry

    Article Title: A mutation in the kringle domain of human factor XII that causes autoinflammation, disturbs zymogen quiescence, and accelerates activation

    doi: 10.1074/jbc.RA119.009788

    Figure Lengend Snippet: Factor XII-W268R displays spontaneous activity during protein expression. A, Western blotting of expression medium under reducing (R) conditions. The closed arrow indicates the FXIIa light chain. The image is representative of three separate experiments. B, chromogenic substrate assay for FXIIa activity in expression medium. C, quantification of FXIIa activity in expression medium. Substrate conversion (linear) was monitored in the first 20 min of the assays and fitted to a standard curve of αFXIIa in expression medium. D, chromogenic substrate assay for plasma prekallikrein activator activity in expression medium. E, effects of PPACK, C1-INH, or antibody OT2 on FXIIa activity in expression medium. F, FXIIa–C1-INH complex formation in expression medium. After incubation with C1-INH, a sigmoidal 4PL fit model was used to interpolate concentrations from a standard curve. The figure panels represent means and S.D. of three repeated experiments.

    Article Snippet: Polyclonal affinity-purified FXII antibody CL20055 was from Cederlane (Burlington, Canada).

    Techniques: Activity Assay, Expressing, Western Blot, Incubation