Mouse PMP22 Antibody Blocking Peptide
€363.00
In stock
SKU
AC-BP16084a
Background:
This gene encodes an integral membrane protein that is amajor component of myelin in the peripheral nervous system. Variousmutations of this gene are causes of Charcot-Marie-Tooth diseaseType IA, Dejerine-Sottas syndrome, and hereditary neuropathy withliability to pressure palsies.
Other Names:
Peripheral myelin protein 22, PMP-22, Growth arrest-specific protein 3, GAS-3, Pmp22, Gas-3, Gas3, Pmp-22
Gene Name: Pmp22
Gene ID: 18858
Primary Accession: P16646
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes an integral membrane protein that is amajor component of myelin in the peripheral nervous system. Variousmutations of this gene are causes of Charcot-Marie-Tooth diseaseType IA, Dejerine-Sottas syndrome, and hereditary neuropathy withliability to pressure palsies.
Other Names:
Peripheral myelin protein 22, PMP-22, Growth arrest-specific protein 3, GAS-3, Pmp22, Gas-3, Gas3, Pmp-22
Gene Name: Pmp22
Gene ID: 18858
Primary Accession: P16646
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
| Is Featured? | No |
|---|
Write Your Own Review