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MYPR Rabbit Polyclonal Antibody, 50ul Endonucleases & Exonucleases This gene is predominantly expressed

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MYPR Rabbit Polyclonal Antibody, 50ul Endonucleases & Exonucleases This gene is predominantly expressedThis gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein may play a role in the compaction stabilization and maintenance of myelin sheaths as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause Pelizaeus Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants including the DM20 splice variant.

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Description

This gene is predominantly expressed in fetal skeletal muscle

Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene

This family of genes encodes multi-pass membrane proteins that are similar to both the chemokine and the transmembrane 4 superfamilies of signaling molecules

This gene encodes an enzyme that belongs to the tyrosine protein kinase family

The related REG1A protein is associated with islet cell regeneration and diabetogenesis

MYPR Rabbit Polyclonal Antibody, 50ul Endonucleases & Exonucleases This gene is predominantly expressedThis gene encodes a transmembrane proteolipid protein that is the predominant component of myelin. The encoded protein may play a role in the compaction stabilization and maintenance of myelin sheaths as well as in oligodendrocyte development and axonal survival. Mutations in this gene cause Pelizaeus Merzbacher disease and spastic paraplegia type 2. Alternatively splicing results in multiple transcript variants including the DM20 splice variant.

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