ARSB Polyclonal Antibody, 50ul Yeast Expression Mutations in this gene result

Mutations in this gene result in Hartnup disorder

Mutations in PKD2 are associated with autosomal dominant polycystic kidney disease type 2

Some of these associations were further supported by gene expression analyses and an association study in essential hypersomnia (EHS)

The protein encoded by AXL (AXL receptor tyrosine kinase) is a member of the Tyro3-Axl-Mer (TAM) receptor tyrosine kinase subfamily

CD300LD (CD300 Molecule Like Family Member D) is a Protein Coding gene

ARSB Polyclonal Antibody, 50ul Yeast Expression Mutations in this gene resultArylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N Acetyl D galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been