MYPR Rabbit Polyclonal Antibody

Ab type

Primary antibody

Background

This 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.

Reactivity

Human, Mouse, Rat

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human MYPR

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

30470

synonyms

MYPR