Emx1 Polyclonal Antibody, 50ul Pipette Controller Mutations in this gene also

Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions

and a minor mediator of the JNK pathway

alcium-dependent phospholipase A2 that selectively hydrolyzes glycerophospholipids in the sn-2 position

Mutations in this gene cause spinocerebellar ataxia type 15

They encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose

Emx1 Polyclonal Antibody, 50ul Pipette Controller Mutations in this gene alsoTranscription factor, which in cooperation with EMX2, acts to generate the boundary between the roof and archipallium in the developing brain. May function in combinations with OTX1 2 to specify cell fates in the developing central nervous system.