I Kappa B Beta Monoclonal Antibody(1F3), 50ul Antibody Development and by CTNNB1 and TCF

and by CTNNB1 and TCF family members in Wnt signaling

Diseases associated with RASGRF1 include bleeding disorder

Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK)

The product of this gene is a membrane-associated guanylate kinase found at the postsynaptic density in neuronal cells

I Kappa B Beta Monoclonal Antibody(1F3), 50ul Antibody Development and by CTNNB1 and TCFThe protein encoded by this gene belongs to the NF kappa B inhibitor family, which inhibit NF kappa B by complexing with, and trapping it in the cytoplasm. Phosphorylation of serine residues on these proteins by kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation of the NF kappa B, which translocates to the nucleus to function as a transcription factor. Alternatively spliced transcript variants have been