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Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), **

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产品名称: Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), **
产品型号: 11-7177-80
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Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), **


Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), **  的详细介绍
Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), **

产品名称:Anti-Mouse/Rat IL-17A FITC (clone eBio17B7), 25 ug
产品货号:eBioscience 11-7177-80
产品规格:25 ug
Anti-Mouse/Rat IL-17A FITC
Also known as: Interleukin-17A, Cytotoxic T-lymphocyte-associated antigen 8
Clone: eBio17B7
RUO: For Research Use Only. Not for use in diagnostic procedures.
SKU# 11-7177
11-7177-80  25 ug
11-7177-81  50 ug 
Description: The eBio17B7 antibody reacts with mouse IL-17A with no recognition of IL-17F. Interleukin-17A (IL-17A) is a CD4+ T cell-derived cytokine that promotes inflammatory responses in cell lines and is elevated in rheumatoid arthritis, asthma, multiple sclerosis, psoriasis, and transplant rejection. The cDNA encoding human IL-17A was isolated from a library of CD4+ T cells; the encoded protein exhibits 72 percent amino acid identity with HVS13 , an open reading frame from a T lymphotropic Herpesvirus saimiri, and 63 percent with mouse CTLA-8 (cytotoxic T-lymphocyte associated antigen-8). Human IL-17A exists as glycosylated 20-30 kD homodimers. High levels of IL-17A homodimer are produced by activated peripheral blood CD4+ T-cells. IL-17A enhances expression of the intracellular adhesion molecule-1 (ICAM-1) in human fibroblasts. Human IL-17A also stimulates epithelial, endothelial, or fibroblastic cells to secrete IL-6, IL-8, G-CSF, and PGE2. In the presence of human IL-17A, fibroblasts can sustain the proliferation of CD34+ hematopoietic progenitors and induce maturation into neutrophils. Mouse, rat, and human IL-17A can induce IL-6 secretion in mouse stromal cells, indicating that all homologs can recognize the mouse IL-17A receptor.
IL-23-dependent, IL-17A-producing CD4+ T cells (Th-17 cells) have been identified as a unique subset of Th cells that develops along a pathway that is distinct from the Th1- and Th2- cell differentiation pathways. The hallmark effector molecules of Th1 and Th2 cells, e.g., IFN gamma and IL-4, have each been found to negatively regulate the generation of these Th-17 cells. 
 

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