IRF-3 Polyclonal Antibody, 100ul[BT-AP10493] Enzyme Activity Assays disease:Defects in AR are the

disease:Defects in AR are the cause of androgen insensitivity syndrome (AIS)

The shorter isoform has been shown to display weaker transforming activity

This gene encodes a protein containing a lines-like domain

The protein encoded by this gene is a GPI degrading enzyme

The C-terminus of the channel is complexed to a PDZ domain protein that is responsible for channel targeting

IRF-3 Polyclonal Antibody, 100ul[BT-AP10493] Enzyme Activity Assays disease:Defects in AR are theThis gene encodes a member of the interferon regulatory transcription factor (IRF) family. The encoded protein is found in an inactive cytoplasmic form that upon serine threonine phosphorylation forms a complex with CREBBP. This complex translocates to the nucleus and activates the transcription of interferons alpha and beta, as well as other interferon induced genes. Alternatively spliced transcript variants encoding multiple isoforms have been