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PMP22 Antibodies
AND PMP22 ELISA kits, PMP22 Proteins
Many biological assays use antibodies to detect PMP22, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with PMP22 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop PMP22 antibodies...
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PMP22 Infographic by Boster Bio
All PMP22 Products
Product
Figures
Specificity
Applications
Price
Human, Mouse, Rat
ELISA
$480
Cat # EKC1478
1 kit, containing one 96-well plate and all necessary reagents
Cat # EKC1478
1 kit, containing one 96-well plate and all necessary reagents
Human, Rat
Flow Cytometry, IHC, ICC, WB
$405
Cat # A00890-1
100ul
Cat # A00890-1
100ul
Human, Mouse, Rat
IHC, WB
$523
Cat # M00890-1
100 µl
Cat # M00890-1
100 µl
PMP22 Overview
Facts about Peripheral myelin protein 22.
Peripheral myelin protein 22 (PMP22)
Might be involved in growth regulation, and in myelinization in the peripheral nervous system. .
Gene Information
| Human | |
|---|---|
| Gene Name: | PMP22 |
| Uniprot: | Q01453 |
| Entrez: | 5376 |
Family
| Belongs to: |
|---|
| PMP-22/EMP/MP20 family |
Alternative Names
CMT1A; CMT1E; GAS3; GAS-3DSS; growth arrest-specific 3; Growth arrest-specific protein 3; HMSNIA; HNPP; MGC20769; peripheral myelin protein 22; PMP-22; Sp110
Molecular Weight
Mass (kDA):
17.891 kDA
Genomic Context
| Human | |
|---|---|
| Location: | 17p12 |
| Sequence: | 17; NC_000017.11 (15229777..15265326, complement) |
Subcellular Localizations
Cell membrane; Multi-pass membrane protein.
Diseases
- Charcot-marie-tooth Disease
- Inherited Neuropathy
- Peripheral Neuropathy
- Hereditary Motor And Sensory Neuropathies
- Hereditary Liability To Pressure Palsies
- Charcot-marie-tooth Disease, Type Ia (disorder)
- Nervousness
- Demyelination
- Polyneuropathy
- Demyelinating Diseases
- Dejerine-sottas Disease (disorder)
- Weakness
Interacting Proteins
- KLRC1
- SMIM3
Pathways
- Myelination
- Pathogenesis
- Cell Proliferation
- Localization
- Regeneration
- Cell Death
- Cell Growth
- Schwann Cell Proliferation
- Muscle Atrophy
- Transport
- Cell Differentiation
- Meiosis
- Cell Adhesion
PTMs
- Glycosylation
- Phosphorylation
- Cleavage
- Ubiquitination
- Methylation
Research Areas
- Cellular Markers
- Glia Markers
- Membrane Trafficking and Chaperones
- Neuroscience
- Oligodendrocyte Cell Markers
For details, visit:
bosterbio.com/bosterbio-gene-info-cards/PMP22
bosterbio.com/bosterbio-gene-info-cards/PMP22
References
PMID: 1303228 by Patel P.I., et al. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
PMID: 1497668 by Hayasaka K., et al. Isolation and sequence determination of cDNA encoding PMP-22 (PAS- II/SR13/Gas-3) of human peripheral myelin.