Emx1 Polyclonal Antibody, 20ul Recombinant Protein Mutations in LMNA lead to

Mutations in LMNA lead to several diseases: Emery-Dreifuss muscular dystrophy

LMWK is not involved in blood coagulation

and it has been proposed that mannose binding by this protein leads to internalization of antigen into Birbeck granules and providing access to a nonclassical antigen-processing pathway

Proteins containing arm repeats are involved in development

and requires a beta subunit called barttin to form a functional channel

Emx1 Polyclonal Antibody, 20ul Recombinant Protein Mutations in LMNA lead toTranscription 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.