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rat anti cd22  (Bio-Rad)


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    Bio-Rad rat anti cd22
    Rat Anti Cd22, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat anti cd22/product/Bio-Rad
    Average 93 stars, based on 9 article reviews
    rat anti cd22 - by Bioz Stars, 2026-03
    93/100 stars

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    Fig. 2. B cell development is altered in Ets-1p/p mice. (A–C) Spleen cells were stained with fluorescent antibodies to B220 and IgM and analyzed by flow cytometry. (D–F) Spleen cells were stained with fluorescent antibodies to IgM and IgD and analyzed by flow cytometry. Mature B cells are indicated by the red box. (G–I) Spleen cells were stained with fluorescent antibodies to CD21 and CD23 and analyzed by flow cytometry. Marginal zone B cells are indicated by the red box and follicular B cells are indicated by the blue box. (J–L) Immunofluorescent staining of B cells (anti- CD22, green) and <t>metallophilic</t> <t>macrophages</t> (anti-Moma-1, red) shows that Ets-1p/p mice have fewer marginal zone B cells (denoted by the white markers), which are normally found surrounding the metallophilic macrophages.
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    Fig. 2. B cell development is altered in Ets-1p/p mice. (A–C) Spleen cells were stained with fluorescent antibodies to B220 and IgM and analyzed by flow cytometry. (D–F) Spleen cells were stained with fluorescent antibodies to IgM and IgD and analyzed by flow cytometry. Mature B cells are indicated by the red box. (G–I) Spleen cells were stained with fluorescent antibodies to CD21 and CD23 and analyzed by flow cytometry. Marginal zone B cells are indicated by the red box and follicular B cells are indicated by the blue box. (J–L) Immunofluorescent staining of B cells (anti- CD22, green) and <t>metallophilic</t> <t>macrophages</t> (anti-Moma-1, red) shows that Ets-1p/p mice have fewer marginal zone B cells (denoted by the white markers), which are normally found surrounding the metallophilic macrophages.
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    Image Search Results


    (A) Aortas after 6 months on the high fat diet showing lipid-rich deposits. (B,C,D) Analysis of lesion size. (E) Sections from the aortic root. Markers: CD4 and CD8, T-cells; CD22, B-cells; CD11b, monocytes, macrophage and neutrophils; smooth muscle actin (αSMA), smooth muscle cells and fibrotic caps. No differences were observed.

    Journal:

    Article Title: Disruption of SEMA4D ameliorates platelet hypersensitivity in dyslipidemia and confers protection against the development of atherosclerosis

    doi: 10.1161/ATVBAHA.109.185405

    Figure Lengend Snippet: (A) Aortas after 6 months on the high fat diet showing lipid-rich deposits. (B,C,D) Analysis of lesion size. (E) Sections from the aortic root. Markers: CD4 and CD8, T-cells; CD22, B-cells; CD11b, monocytes, macrophage and neutrophils; smooth muscle actin (αSMA), smooth muscle cells and fibrotic caps. No differences were observed.

    Article Snippet: Acetone fixed and peroxidase quenched sections were incubated with biotinylated rat anti-mouse CD4 and rat anti-mouse CD8 (made in-house), rat anti-mouse CD22 (Southern Biotech, Birmingham, AL) and rat anti-mouse CD11b (BD Biosciences, Pasadena, CA) and FITC-conjugated mouse anti-α-smooth muscle actin (SMA) clone 14A (Sigma, St. Louis, MO).

    Techniques:

    Fig. 2. B cell development is altered in Ets-1p/p mice. (A–C) Spleen cells were stained with fluorescent antibodies to B220 and IgM and analyzed by flow cytometry. (D–F) Spleen cells were stained with fluorescent antibodies to IgM and IgD and analyzed by flow cytometry. Mature B cells are indicated by the red box. (G–I) Spleen cells were stained with fluorescent antibodies to CD21 and CD23 and analyzed by flow cytometry. Marginal zone B cells are indicated by the red box and follicular B cells are indicated by the blue box. (J–L) Immunofluorescent staining of B cells (anti- CD22, green) and metallophilic macrophages (anti-Moma-1, red) shows that Ets-1p/p mice have fewer marginal zone B cells (denoted by the white markers), which are normally found surrounding the metallophilic macrophages.

    Journal: International immunology

    Article Title: Ets-1 deficiency leads to altered B cell differentiation, hyperresponsiveness to TLR9 and autoimmune disease.

    doi: 10.1093/intimm/dxh295

    Figure Lengend Snippet: Fig. 2. B cell development is altered in Ets-1p/p mice. (A–C) Spleen cells were stained with fluorescent antibodies to B220 and IgM and analyzed by flow cytometry. (D–F) Spleen cells were stained with fluorescent antibodies to IgM and IgD and analyzed by flow cytometry. Mature B cells are indicated by the red box. (G–I) Spleen cells were stained with fluorescent antibodies to CD21 and CD23 and analyzed by flow cytometry. Marginal zone B cells are indicated by the red box and follicular B cells are indicated by the blue box. (J–L) Immunofluorescent staining of B cells (anti- CD22, green) and metallophilic macrophages (anti-Moma-1, red) shows that Ets-1p/p mice have fewer marginal zone B cells (denoted by the white markers), which are normally found surrounding the metallophilic macrophages.

    Article Snippet: Spleen sections were incubated with a combination of biotinylated mouse antimouse CD22 (Cy34, BD Biosciences) and rat anti-mouse metallophilic macrophage mAb (Moma-1; Serotec, Raleigh, NC, USA).

    Techniques: Staining, Cytometry