IRAK-4 Monoclonal Antibody, 100ul sgRNA customized design which is associated with Borjeson-Forssman-Lehmann

which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS)

Tumor necrosis factor receptor type 1-associated DEATH domain protein binds adaptor protein TRAF2

Mutations in RAD50 are the cause of Nijmegen breakage syndrome-like disorder

ANO2 belongs to a family of calcium-activated chloride channels (CaCCs) (reviewed by Hartzell et al

Phosphorylated cooperatively by ROCK1 and CDC42BP on Thr-696

IRAK-4 Monoclonal Antibody, 100ul sgRNA customized design which is associated with Borjeson-Forssman-LehmannThis gene encodes a kinase that activates NF kappaB in both the Toll like receptor (TLR) and T cell receptor (TCR) signaling pathways. The protein is essential for most innate immune responses. Mutations in this gene result in IRAK4 deficiency and recurrent invasive pneumococcal disease. Multiple transcript variants encoding different isoforms have been found for this gene.