LMX1B Polyclonal Antibody, 50ul Shakers dermis and tendon

dermis and tendon

LRRK1 (leucine-rich repeat serine/threonine-protein kinase 1)

Mutations have also been associated with non-insulin-dependent diabetes mellitus type II| an autosomal dominant disease of defective insulin secretion

spermatogenesis

This gene utilizes alternative polyadenylation signals and has multiple pseudogenes

LMX1B Polyclonal Antibody, 50ul Shakers dermis and tendonLMX1B encodes a member of LIM homeodomain family of proteins containing two N terminal zinc binding LIM domains, 1 homeodomain, and a C terminal glutamine rich domain. It functions as a transcription factor, and is essential for the normal development of dorsal limb structures, the glomerular basement membrane, the anterior segment of the eye, and dopaminergic and serotonergic neurons. Mutations in this gene are associated with nail patella syndrome.