Galactosidase Beta1L3 Polyclonal Antibody, 20ul Buffer Solutions Defects in this gene are

Defects in this gene are the cause of ovarian dysgenesis 2

CA VA is localized in the mitochondria and expressed primarily in the liver

These openings also allow standard pipettes be able to added or removed samples from the bottom compartment

2001 [PubMed 11689425])

Galactosidase Beta1L3 Polyclonal Antibody, 20ul Buffer Solutions Defects in this gene areGLB1L3 (Galactosidase Beta 1 Like 3) is a Protein Coding gene. Diseases associated with GLB1L3 include leber congenital amaurosis. GO annotations related to this gene include hydrolase activity, hydrolyzing O glycosyl compounds and beta galactosidase activity. An important paralog of this gene is GLB1L2.