MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint for

The chromosome 22 breakpoint for this translocation is located within the BCR gene (BCR

The type I hair keratins are clustered in a region of chromosome 17q12-q21 and have the same direction of transcription

This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity

|PTM:While translation occurs| the particular unfolded structure after the GRR repeat promotes the generation of p52 making it an acceptable substrate for the proteasome

a Ras-responsive E3 ubiquitin ligase

MNX1 Polyclonal Antibody, 50ul Sealing Film The chromosome 22 breakpoint forThis gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.