PMP2 Protein (Myc-DYKDDDDK Tag)
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- Target See all PMP2 Proteins
- PMP2 (Peripheral Myelin Protein 2 (PMP2))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This PMP2 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human PMP2 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product PMP2 Protein
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Peripheral Myelin Protein 2 (PMP2) (AA 2-132) protein (His tag)
PMP2 Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 95 % by SDS-PAGE gel analyses WB, ELISA
Peripheral Myelin Protein 2 (PMP2) (AA 2-132) protein (His tag)Crystallography grade PMP2 Origin: Mouse Host: Escherichia coli (E. coli) Recombinant >95 % as determined by SDS PAGE, Size Exclusion Chromatography and Western Blot. SDS, WB, ELISA, Crys
Peripheral Myelin Protein 2 (PMP2) (AA 1-132), (full length) protein (GST tag)PMP2 Origin: Human Host: Escherichia coli (E. coli) Recombinant 90 % ELISA
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Target
- PMP2 (Peripheral Myelin Protein 2 (PMP2))
- Alternative Name
- Pmp2 (PMP2 Products)
- Synonyms
- FABP8 Protein, M-FABP Protein, MP2 Protein, P2 Protein, peripheral myelin protein 2 Protein, PMP2 Protein, Pmp2 Protein
- Background
- The protein encoded by this gene localizes to myelin sheaths of the peripheral nervous system. The encoded protein can bind both the membrane layers of the sheaths and monomeric lipids, and is thought to provide stability to the sheath. A defect in this gene was shown to be a cause of dominant demyelinating CMT neuropathy.
- Molecular Weight
- 14.7 kDa
- NCBI Accession
- NP_002668
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