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    human CD20 (bsm-30098M-APC-Cy7)  
    訂購熱線(xiàn):400-901-9800
    訂購郵箱:sales@bioss.com.cn
    訂購QQ:  400-901-9800
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    100T/3880.00元
    大包裝/詢(xún)價(jià)
    產(chǎn)品編號 bsm-30098M-APC-Cy7
    英文名稱(chēng) human CD20
    中文名稱(chēng) APC-Cy7標記的小鼠抗人CD20單克隆抗體
    抗體來(lái)源 Mouse
    克隆類(lèi)型 Monoclonal
    克 隆 號 HI20a
    交叉反應 Human
    產(chǎn)品應用 Flow-Cyt=10ul/Test
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    細胞定位 細胞膜 
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human CD20 
    亞    型 Mouse IgG2a
    純化方法 affinity purified by Protein G
    緩 沖 液 0.01M PBS (pH7.4), 0.5% BSA, 0.02% Proclin300.
    保存條件 Store at 2-8℃. Protect from light. Avoid freezing.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產(chǎn)品介紹 CD20 is a non glycosylated protein with a molecular weight of 35 or 37 kDa depending on the degree of phosphorylation. Although not a member of the tetraspanin superfamily of cell surface receptors, it crosses the cell membrane four times. The CD20 antigen is present on human pre B lymphocytes and on B lymphocytes at all stages of maturation, except on plasma cells. Low level expression of the CD20 antigen has been detected on normal T lymphocytes. The CD20 molecule is involved in regulation of B cell differentiation, presumably via its reported function as a Ca++ channel subunit.

    Function:
    This protein may be involved in the regulation of B-cell activation and proliferation

    Subcellular Location:
    Membrane; Multi-pass membrane protein.

    Tissue Specificity:
    Phosphorylated. Might be functionally regulated by protein kinase(s).

    Post-translational modifications:
    Membrane; Multi-pass membrane protein.

    DISEASE:
    Defects in MS4A1 are the cause of immunodeficiency common variable type 5 (CVID5) [MIM:613495]; also called antibody deficiency due to CD20 defect. CVID5 is a primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antigen. The defect results from a failure of B-cell differentiation and impaired secretion of immunoglobulins; the numbers of circulating B-cells is usually in the normal range, but can be low.

    Similarity:
    Belongs to the MS4A family.

    Database links:

    Entrez Gene : 931 Human

    SwissProt : P11836 Human



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