Hexb Polyclonal Antibody, 50ul Protein Expression Defects in this gene are

Defects in this gene are a cause of familial hypercholanemia (FHCA)

ADAM32 is located in a cluster of other disintegrin and metallopeptidase family genes on chromosome 8

It is uncertain whether Met-1 or Met-50 is the initiator

This complex is composed partly of two structural maintenance of chromosomes (SMC) proteins

Hexb Polyclonal Antibody, 50ul Protein Expression Defects in this gene areHexosaminidase B is the beta subunit of the lysosomal enzyme beta hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N acetyl hexosamines. Beta hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases.