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Anti-Human CD7 APC (124-1D1) **

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產(chǎn)品名稱: Anti-Human CD7 APC (124-1D1) **
產(chǎn)品型號: 17-0079-42
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Anti-Human CD7 APC (124-1D1) **


Anti-Human CD7 APC (124-1D1) **  的詳細(xì)介紹
Anti-Human CD7 APC (124-1D1) **

產(chǎn)品名稱:Anti-Human CD7 APC (124-1D1) 100 tests
產(chǎn)品貨號:eBioscience 17-0079-42
產(chǎn)品規(guī)格:100 tests
Anti-Human CD7 APC
Also known as: Leu-9
Clone: eBio124-1D1 (124-1D1)
RUO: For Research Use Only. Not for use in diagnostic procedures.
SKU# 17-0079
Cat. No. Size
17-0079-42  100 tests 
Description: The eBio124-1D1 monoclonal antibody reacts with human CD7, also known as gp40 and Leu9. CD7, a 40 kD receptor, is a member of the immunoglobulin gene superfamily. The N-terminal amino acid sequence (aa1-107) is highly homologous to Ig kappa light chain sequence; while the carboxyl-terminal region of the extracellular domain is proline-rich and has been postulated to form a stalk from which the Ig domain projects. CD7 is expressed on the majority of immature and mature T lymphocytes, and T cell leukemias. It is also found on natural killer cells, a small suppopulation of normal B cells and on maligant B cells. Cross-linking surface CD7 positively modulates T cell and NK cell activity, as measured by calcium flux, expression of adhesion molecules, cytokine secretion and proliferation. CD7 associates directly with phosphoinositol 3'-kinase. CD7 ligation induces production of D-3 phosphoinositides and tyrosine phosphorylation.
A clonogenic subpopulation of human CD34(+) CD38(-) cord blood cells that express CD45RA and HLA-DR and high levels of the CD7 has been reported. These cells possess the capacity for lymphopoiesis. They can generate B-cells, natural killer cells, and dendritic cells but do not possess the capacity to develop into myeloid cells or erythroid cells. The CD7(+) phenotype distinguishes primitive human lymphoid progenitors from pluripotent stem cells.
Furthermore, it has been suggested that CD7 co-operates with CD28 during Treg function, as mice deficient in both CD28 and CD7 have reduced total numbers of Tregs and these Tregs have reduced suppressive activity.

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