RAG-1 inhibitors comprise a diverse group of chemicals that indirectly modulate the activity of the Recombination Activating Gene 1 (RAG-1) protein by targeting signaling pathways critical for immune responses. Tofacitinib, Ibrutinib, and Ruxolitinib act on the JAK-STAT signaling pathway, which is intricately connected to processes regulated by RAG-1. These inhibitors interfere with cellular processes involved in immune responses, impacting RAG-1-mediated pathways and contributing to the inhibition of RAG-1 function in specific cellular contexts.
Similarly, Baricitinib, Acalabrutinib, and Fedratinib, through their effects on JAKs and BTK, indirectly influence RAG-1 by disrupting signaling cascades related to B-cell development. Dasatinib, TAK-242, VX-745, TPCA-1, SB 203580, and Bay 11-7082 target various signaling pathways, such as p38 MAP kinase and NF-κB, that intersect with RAG-1-mediated processes. The broad spectrum of these inhibitors allows for the modulation of immune responses and RAG-1 function in specific cellular contexts. In summary, RAG-1 inhibitors offer a range of options to researchers studying immune-related processes, providing insights into dysregulated immune responses. The detailed understanding of their biochemical interactions emphasizes their significance in elucidating the complexities of immune regulation and the role of RAG-1 in these intricate cellular pathways.
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