I Kappa B Beta Monoclonal Antibody(1F3), 20ul Cell Culture Dishes SCGB2A1 is a Protein Coding

SCGB2A1 is a Protein Coding gene

a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death

1 µl to 10 ml

It contains two transcript variants diverging at the 5' termini

Mutations in ADIPOQ are associated with adiponectin deficiency

I Kappa B Beta Monoclonal Antibody(1F3), 20ul Cell Culture Dishes SCGB2A1 is a Protein CodingThe 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