Code | CSB-YP011811MO |
MSDS | |
Size | Pls inquire |
Source | Yeast |
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Code | CSB-EP011811MO-B |
MSDS | |
Size | Pls inquire |
Source | E.coli |
Conjugate | Avi-tag Biotinylated E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag. |
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Code | CSB-MP011811MO |
MSDS | |
Size | Pls inquire |
Source | Mammalian cell |
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This Recombinant mouse interleukin-1 receptor-associated kinase 3 (IRAK3) is a semi-custom product. There are 5 expression system options: Yeast, E. coli, In Vivo Biotinylation in E. coli, Baculovirus, and Mammalian cell. Your requirements will be given top priority in determining the protein tags. For proteins within 800 aa, risk-free custom service is guaranteed. It means you will not be charged if the protein cannot be delivered.
IRAK3 is a kinase-deficient member of the TLR/IRAK family that acts as a crucial negative regulator of TLR-mediated cell signaling [1]. IRAK3 plays a significant role in inhibiting inflammation in conditions like obesity and metabolic syndrome [1]. It is involved in the TLR/IL-1 receptor signaling pathway and is essential for innate immune responses and inflammation [2]. IRAK3 regulates TLRs and IL-1Rs signaling in immune and inflammatory responses [3].
The IRAK family, including IRAK3, is pivotal in regulating TLR and IL-1 signaling pathways, which are crucial for sensing pathogens and initiating immunity and inflammation. IRAK3 is part of the IRAK family that can be recruited to the TLR complex to mediate diverse downstream signaling. It negatively modulates TLR-mediated cell signaling, highlighting its importance in controlling immune responses [1].
References:
[1] M. Hulsmans, B. Geeraert, D. Keyzer, A. Mertens, M. Lannoo, B. Vanaudenaerdeet al., Interleukin-1 receptor-associated kinase-3 is a key inhibitor of inflammation in obesity and metabolic syndrome, Plos One, vol. 7, no. 1, p. e30414, 2012. https://doi.org/10.1371/journal.pone.0030414
[2] S. Flannery and A. Bowie, The interleukin-1 receptor-associated kinases: critical regulators of innate immune signalling, Biochemical Pharmacology, vol. 80, no. 12, p. 1981-1991, 2010. https://doi.org/10.1016/j.bcp.2010.06.020
[3] L. Ringwood and L. Li, The involvement of the interleukin-1 receptor-associated kinases (iraks) in cellular signaling networks controlling inflammation, Cytokine, vol. 42, no. 1, p. 1-7, 2008. https://doi.org/10.1016/j.cyto.2007.12.012"
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