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human CD20 (bsm-30098M-APC-Cy7)  
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100T/3880.00元
大包裝/詢(xún)價(jià)
產(chǎn)品編號(hào) bsm-30098M-APC-Cy7
英文名稱(chēng) human CD20
中文名稱(chēng) APC-Cy7標(biāo)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(hào) HI20a
交叉反應(yīng) Human
產(chǎn)品應(yīng)用 Flow-Cyt=10ul/Test
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
細(xì)胞定位 細(xì)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(xiàng) 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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