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    human CD20 Mouse mAb (bsm-30098M)  
    訂購熱線(xiàn):400-901-9800
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    訂購QQ:  400-901-9800
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    100ug/1880.00元
    大包裝/詢(xún)價(jià)

    產(chǎn)品編號 bsm-30098M
    英文名稱(chēng) human CD20 Mouse mAb
    中文名稱(chēng) 小鼠抗人CD20單克隆抗體
    別    名 CD20_HUMAN; B-lymphocyte antigen CD20; B-lymphocyte surface antigen B1; Bp35; Leukocyte surface antigen Leu-16; Membrane-spanning 4-domains subfamily A member 1; MS4A1; MS4A2; B1; CVID5; LEU-16; S7.  
    研究領(lǐng)域 腫瘤  免疫學(xué)  干細胞  細胞表面分子  b-淋巴細胞  
    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=2ug/Test
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 33 kDa
    檢測分子量 33-37
    細胞定位 細胞膜 
    性    狀 Liquid
    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 TBS (pH7.4).
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    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 This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This gene encodes a B-lymphocyte surface molecule which plays a role in the development and differentiation of B-cells into plasma cells. This family member is localized to 11q12, among a cluster of family members. Alternative splicing of this gene results in two transcript variants which encode the same protein. [provided by RefSeq, Jul 2008]

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

    Subcellular Location:
    Membrane; Multi-pass membrane protein.

    Tissue Specificity:
    Expressed on B-cells.

    Post-translational modifications:
    Phosphorylated. Might be functionally regulated by protein kinase(s).

    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.

    SWISS:
    P11836

    Gene ID:
    931

    Database links:

    Entrez Gene: 931 Human

    Omim: 112210 Human

    SwissProt: P11836 Human

    Unigene: 712553 Human



    產(chǎn)品圖片
    Blank control:whole blood. Primary Antibody (green line): Mouse Anti-CD20 antibody (bsm-30098M) Dilution: 2ul/Test; Secondary Antibody : Goat anti-Mouse IgG-FITC Dilution: 0.5ug/Test. Protocol Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
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