DYM Rabbit Polyclonal Antibody, 50ul Peptide Modification but it may play protective

but it may play protective or modulatory roles during late embryogenesis and postnatal development

Excellent chemical resistance

Mutations in this gene may result in Netherton syndrome

The protein is active alone or as a heteromultimeric assembly with TRPC1| TRPC3| and TRPC4

The encoded protein (chloride voltage-gated channel Ka) is predicted to have 12 transmembrane domains

DYM Rabbit Polyclonal Antibody, 50ul Peptide Modification but it may play protectiveThis gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia Dyggve Melchior Clausen (DMC) dysplasia and Smith McCort (SMC) dysplasia which involve both skeletal defects and mental retardation.