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.

Classification:

Primary antibody

Alternative names:

MYPR

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human MYPR

Concentration:

1 mg/ml

Molecular weight:

30470

Applications:

WB

Storage:

-20°C for 1 year

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