LETM1

gene product
SLC55A1
This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19. [provided by RefSeq, Oct 2009]
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243 antibodies from 26 providers.

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Novus Biologicals
8 antibodies
Abnova Corporation
7 antibodies
antibodies-online
82 antibodies
Atlas Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
49 antibodies
Proteintech Group
1 antibody
Abgent
2 antibodies
NovoPro Bioscience Inc.
1 antibody
Biorbyt
9 antibodies
Aviva Systems Biology
4 antibodies
OriGene
2 antibodies
GeneTex
1 antibody
Invitrogen Antibodies
3 antibodies
Signalway Antibody LLC
1 antibody
Affinity Biosciences
1 antibody
Bethyl Laboratories
1 antibody
Creative Biolabs
9 antibodies
Creative Diagnostics
2 antibodies
RayBiotech, Inc.
1 antibody
United States Biological
45 antibodies
MyBioSource
3 antibodies
Sigma-Aldrich
4 antibodies
ProSci
2 antibodies
Boster Biological Technology
1 antibody
RabMAbs
1 antibody
St John's Laboratory
1 antibody