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eBioscience 13-7496-85 anti-human TSLP polyclonal Biotin 500 ug

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產品名稱: eBioscience 13-7496-85 anti-human TSLP polyclonal Biotin 500 ug
產品型號: 13-7496-85
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eBioscience 13-7496-85 anti-human TSLP polyclonal Biotin 500 ug


eBioscience 13-7496-85 anti-human TSLP polyclonal Biotin 500 ug  的詳細介紹
eBioscience 13-7496-85 anti-human TSLP polyclonal Biotin 500 ug

產品名稱:anti-human TSLP polyclonal Biotin 500 ug
產品貨號:eBioscience 13-7496-85
產品規(guī)格:500 ug
Anti-Human TSLP Biotin
Also known as: Thymic Stromal-Derived Lymphopoietin
RUO: For Research Use Only. Not for use in diagnostic procedures.
SKU# 13-7496
Cat. No. Size
13-7496-81  50 ug 
13-7496-85  500 ug 
Description: The polyclonal anti-human TSLP antibody reacts with human thymic stromal lymphopoietin (TSLP). TSLP is an IL-7-like cytokine derived from epithelial cells, which strongly activates dendritic cells (DC). TSLP can replace the activity of IL-7 in supporting the development of B cells in vitro; it promotes the proliferation and differentiation of committed B220(+) B cell progenitors. TSLP prevents cell death by apoptosis and stimulates growth of the human acute myeloid leukemia cell line MUTZ-3. This effect is neutralized by antibodies directed against IL-7. The TSLP receptor has been shown to be a member of the hematopoietin receptor superfamily. High affinity binding sites require the presence of the alpha chain of the IL-7 receptor (CD127). The receptor complex does not involve the common gamma chain (CD132), a signal-transducing component of various cytokine receptors, including receptors for IL-4, IL-7, IL-9, IL-13, and IL-15. Recently TSLP has been found expressed by keratinocytes of atopic dermatitis; TSLP expression is also associated with Langerhans cell migration and activation in situ. TSLP expressed within thymus and peripheral lymphoid and non-lymphoid tissues regulates DC-mediated central tolerance, peripheral T cell homeostasis, and inflammatory Th2 responses. DCs activated by TSLP can prime naïve CD4 T cells to differentiate into T helper type 2 cells that produce high levels of TNF-a, but no IL-10. This priming for Th2 differentiation is dependent upon TSLP-mediated upregulation of OX40L by DCs.
 

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