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| 规格: | 25μg | 产品价格: | ¥1680.0 |
|---|---|---|---|
| 规格: | 100μg | 产品价格: | ¥3600.0 |
| 规格: | 500μg | 产品价格: | ¥9800.0 |
OX40, a member of the TNF receptor family, is primarily recognized for its role in promoting effector T cell differentiation, proliferation, long-term survival, and the production of pro-inflammatory cytokines. It also inhibits the differentiation and suppressive activity of regulatory T cells (Tregs). OX40 is expressed on activated CD4+ and CD8+ T cells, as well as on other cell types. The OX40 ligand, expressed by antigen-presenting cells (APCs), activates the OX40 signaling pathway, which enhances the immune response. The interaction between OX40 and its ligand leads to increased CD4+ and CD8+ cell proliferation, stimulated cytokine production, and improved survival of antigen-specific memory T cells. OX40 expression has been identified as an unfavorable prognostic marker and may be a potential target for future immunotherapies. In the context of esophageal carcinoma (EC), OX40 has been identified as a novel molecule; its elevated expression is associated with favorable clinical outcomes. As a second immune checkpoint, OX40 may have significant implications for the prognosis and immunomodulation of EC patients. In mice, the absence of OX40 results in a significant reduction in the number of effector memory CD4+ cells and a diminished CD8+ response, leading to accelerated tumor growth. Consequently, the immune-stimulating properties of OX40 agonists could potentially counteract some of the immunosuppressive properties within the tumor environment.
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文献和实验Identifying Protein Interactions by Hydroxyl‐Radical Protein Footprinting
is then cleaved in the absence and presence of ligand. Cleavage products are separated by high resolution gel electrophoresis. The digital image of the footprinting gel can be subjected to quantitative analysis to identify changes in the sensitivity of the protein
purification of protein complexes, in combination with in vivo biotinylation of critical transcription factors, has contributed to the analysis of the pluripotent state in mouse embryonic stem (ES) cells and made it possible to construct a protein?protein
.3 ). Concatamers of tags are cloned and sequenced to yield a STAGE library. Tags in the library represent DNA fragments that were occupied by the DNA?binding protein, and mapping these tag sequences to the genome identifies the binding loci of the DNA?binding
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