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The classical pathway for activation of NF-kB, a key transcriptional regulator of the immune system, is controlled by the IKK complex. Activated IKK phosphorylates IkB which is ubiquitinated and rapidly degraded, allowing NF-kB to translocate from the cytoplasm to the nucleus where it activates gene transcription. However, the mechanisms regarding IKK activation have been elusive.
Now CARMA1, Bcl-10, and MALT1 are helping to fill in the blanks of IKK activation. These proteins are downstream of the T cell receptor (TCR) and upstream of the IKK complex (Fig. 1). Antigen-TCR signaling in the adaptive immune system leads to PKC-q activation and formation of an oligomerization-ubiquitination (Ub)-phosphorylation (P) pathway leading to activated IKK. Oligomerization-Ub-P pathways have also been found to mediate NF-kB activation through TLR (Toll-like receptor) signaling, suggesting these emerging IKK activation pathways may play key roles in regulating both adaptive and innate immunity.
IMGENEX offers a complete line of antibodies, inhibitors, ELISA assays, and RNAi kits to complement your NF-kB & TLR signaling studies. Visit our website to learn how we can help you accelerate your research.
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TCR Pathway
 FIGURE 1. IKK activation in T cells is controlled by an oligomerization-ubiquitination (Ub)-phosphorylation pathway.
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MALT1/Paracaspase (IMG-5745)

IHC analysis of MALT1/Paracaspase expression in formalin-fixed human reactive lymph node using IMG-5745 at 1:2000.
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