MPZ Protein (AA 30-153) (His tag)
Quick Overview for MPZ Protein (AA 30-153) (His tag) (ABIN2746043)
Target
See all MPZ ProteinsProtein Type
Origin
Source
Purity
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Protein Characteristics
- AA 30-153
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Purification tag / Conjugate
- This MPZ protein is labelled with His tag.
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Purpose
- Recombinant Human Myelin Protein P0/MPZ (C-6His)
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Sequence
- IVVYTDREVH GAVGSRVTLH CSFWSSEWVS DDISFTWRYQ PEGGRDAISI FHYAKGQPYI DEVGTFKERI QWVGDPRWKD GSIVIHNLDY SDNGTFTCDV KNPPDIVGKT SQVTLYVFEK VPTRVDHHHH HH
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Characteristics
- Recombinant Human Myelin Protein P0/MPZ is produced by our mammalian expression system in human cells. The target protein is expressed with sequence (Ile30-Arg153) of Human MPZ fused with a 6His tag at the C-terminus.
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Sterility
- 0.2 μm filtered
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Endotoxin Level
- Less than 0.1 ng/μg (1 IEU/μg) as determined by LAL test
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
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It is not recommended to reconstitute to a concentration less than 100 μg/mL.
Dissolve the lyophilized protein in ddH2O.
Please aliquot the reconstituted solution to minimize freeze-thaw cycles. -
Buffer
- Lyophilized from a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.2.
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Handling Advice
- Always centrifuge tubes before opening. Do not mix by vortex or pipetting.
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Storage
- 4 °C/-20 °C/-80 °C
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Storage Comment
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Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks.
Reconstituted protein solution can be stored at 4-7°C for 2-7 days.
Aliquots of reconstituted samples are stable at < -20°C for 3 months. -
Expiry Date
- 3 months
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- MPZ (Myelin Protein Zero (MPZ))
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Alternative Name
- Myelin-protein-P0
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Sub Type
- Fusionprotein
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Background
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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.
Alternative Names: Myelin Protein P0, Myelin Peripheral Protein, MPP, Myelin Protein Zero, MPZ -
Molecular Weight
- 15.2 kDa
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UniProt
- P25189
Target
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