PMP22

gene product
CMT1A, GAS3, HMSNIA, HNPP, Sp110
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. [provided by RefSeq, Jul 2013]
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382 antibodies from 33 providers.

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Invitrogen Antibodies
8 antibodies
Novus Biologicals
25 antibodies
antibodies-online
119 antibodies
LifeSpan BioSciences, Inc.
79 antibodies
OriGene
14 antibodies
Aviva Systems Biology
3 antibodies
Affinity Biosciences
1 antibody
Biorbyt
19 antibodies
Acris Antibodies GmbH
8 antibodies
GeneTex
6 antibodies
Abnova Corporation
4 antibodies
Bioworld Technology, Inc
1 antibody
St John's Laboratory
2 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Creative Biolabs
12 antibodies
Arigo
4 antibodies
MyBioSource
5 antibodies
Spring Bioscience
4 antibodies
Creative Diagnostics
5 antibodies
ProSci
2 antibodies
RabMAbs
2 antibodies
Sigma-Aldrich
2 antibodies
Abbiotec
1 antibody
Boster Biological Technology
1 antibody
NovoPro Bioscience Inc.
1 antibody
United States Biological
27 antibodies
Abbexa
3 antibodies
GenWay
3 antibodies
Abgent
1 antibody
EMD Millipore
1 antibody
Leading Biology
1 antibody
RayBiotech, Inc.
1 antibody