Search results for MPZ antibody

MPZ antibody, C-term, Genetex, GTX81135

Myelin Protein P0 (MPZ) Antibody, Abbexa, abx403249

Human Myelin Protein P0 (MPZ) Antibody is a Mouse monoclonal against Myelin Protein P0 (MPZ).

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx174293

Protein Zero, Myelin (MPZ) Antibody is a Mouse Monoclonal antibody against Protein Zero, Myelin (MPZ).

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx034032

MPZ is a major structural protein of peripheral myelin. Creation of an extracellular membrane face which guides the wrapping process and ultimately compacts adjacent lamellae.

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx113908

Myelin Protein Zero Antibody is a Rabbit Polyclonal antibody against Myelin Protein Zero.

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx110015

Myelin protein P0 Antibody is a Rabbit Polyclonal antibody against Myelin protein P0.

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx174294

This product is currently in development. The lead time for this product may be several months. Please contact us at [email protected] for an updated lead time before purchasing this product. Protein Zero, Myelin (MPZ) Antibody is a Mouse Monoclonal antibody against Protein Zero, Myelin (MPZ).

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx213713

MPZ Antibody is a Rabbit Polyclonal against MPZ.

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx101915

Polyclonal Antibody to Protein Zero, Myelin (MPZ).

Protein Zero, Myelin (MPZ) Antibody, Abbexa, abx001415

MPZ Antibody is a Rabbit Polyclonal antibody against MPZ. MPZ (myelin protein zero), also known as P0, a transmembrane glycoprotein (~30 kDa), is a member of the immunoglobulin supergene family. Synthesized by myelin-forming Schwann cells, MPZ is the major structural protein component of myelin in the peripheral nervous system. It is involved in formation and maintenance of compact myelin, and plays a role in the creation of an extracellular membrane face which guides the wrapping process and ultimately compacts adjacent lamellae. More than 120 mutations detected in the gene of MPZ cause various forms of hereditary neuropathy, which include Charcot-Marie-Tooth disease type 1B (CMT1B), CMT2, Dejerine-Sottas syndrome (DSS), and congenital hypomyelination neuropathy (CHN). This antibody can recognize endogenous MPZ, and can be used as a marker of myelinating Schwann cells.