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Recombinant Human Myelin Protein P0/MPZ Protein (His Tag)– MSE Supplies LLC

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Recombinant Human Myelin Protein P0/MPZ Protein (His Tag)

SKU: PKSH032770-50

  • $ 47095
  • Save $ 5300



Recombinant Human Myelin Protein P0/MPZ Protein (His Tag)

 

SKU # PKSH032770
Expression Host HEK293 Cells

 

 

Description

Synonyms MPP, MPZ, Myelin Peripheral Protein, Myelin Protein P0, Myelin Protein Zero
Species Human
Expression Host HEK293 Cells
Sequence Ile30-Arg153
Accession P25189
Calculated Molecular Weight 15.2 kDa
Observed Molecular Weight 14-17 kDa
Tag C-His
Bio-activity Not validated for activity
  

 

Properties

Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from a 0.2 μm filtered solution of PBS, pH 7.4.
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.



Background

Myelin Protein P0 (MPZ) is a single-pass type I membrane glycoprotein which belongs to the myelin P0 protein family. MPZ contains one Ig-like V-type (immunoglobulin-like) domain, absent in the central nervous system. MPZ is a major component of the myelin sheath in peripheral nerves. It is postulated that MPZ is a structural element in the formation and stabilisation of peripheral nerve myelin, holding its characteristic coil structure together by the interaction of its positively-charged domain with acidic lipids in the cytoplasmic face of the opposed bilayer, and by interaction between hydrophobic globular of adjacent extracellular domains. Defects in MPZ associated with Charcot-Marie-Tooth disease and Dejerine-Sottas disease.