LSR Polyclonal Antibody, 100ul Cryopreservation Mutations in CDKN1B are associated

Mutations in CDKN1B are associated with multiple endocrine neoplasia type IV (MEN4)

also known as autosomal dominant speech and language disorder with orofacial dyspraxia

The protein encoded by CNTNAP3 (contactin associated protein-like 3) belongs to the NCP family of cell-recognition molecules

The encoded protein primarily localizes to the centrosome

|subunit:Heterodimer with JUN

LSR Polyclonal Antibody, 100ul Cryopreservation Mutations in CDKN1B are associatedIn contrast to the rodent orthologous protein, it is longer in N terminus and no signal sequence is detected by any prediction method.,The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.,Probable role in the clearance of triglyceride rich lipoprotein from blood. Binds chylomicrons, LDL and VLDL in presence of free fatty acids and allows their subsequent uptake in the