Nicalin Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification a rare congenital disorder

a rare congenital disorder

The gene is a tumor suppressor gene candidate and a negative regulator of the Ras-p42/44 mitogen-activated kinase cascade

The deficient mice exhibited defects in early differentiation of T and B lymphocytes

Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H)| a disorder of the peripheral nervous system

This protein is a cell growth-related protein

Nicalin Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification a rare congenital disorderNCLN (Nicalin) is a Protein Coding gene. May antagonize Nodal signaling and subsequent organization of axial structures during mesodermal patterning.