PMP22 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
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- Target See all PMP22 Proteins
- PMP22 (Peripheral Myelin Protein 22 (PMP22))
- Protein Type
- Recombinant
- Protein Characteristics
- Transcript Variant 3
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This PMP22 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human PMP22 (transcript variant 3) 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 PMP22 Protein
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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
- PMP22 (Peripheral Myelin Protein 22 (PMP22))
- Alternative Name
- Pmp22 (PMP22 Products)
- Synonyms
- CMT1A Protein, CMT1E Protein, DSS Protein, GAS-3 Protein, HMSNIA Protein, HNPP Protein, Sp110 Protein, 22kDa Protein, Gas-3 Protein, Tr Protein, trembler Protein, pmp22 Protein, wu:fa04d03 Protein, wu:fa08d03 Protein, MGC80653 Protein, PMP22 Protein, MGC69407 Protein, id:ibd2630 Protein, wu:fb81f09 Protein, zgc:136919 Protein, peripheral myelin protein 22 Protein, peripheral myelin protein 22a Protein, peripheral myelin protein 22 S homeolog Protein, peripheral myelin protein 22b Protein, PMP22 Protein, Pmp22 Protein, pmp22a Protein, pmp22.S Protein, pmp22 Protein, pmp22b Protein
- Background
- This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants.
- Molecular Weight
- 17.7 kDa
- NCBI Accession
- NP_696997
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