LOXL3

gene product
This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
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184 antibodies from 21 providers.

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antibodies-online
50 antibodies
Novus Biologicals
26 antibodies
NovoPro Bioscience Inc.
1 antibody
Biorbyt
13 antibodies
LifeSpan BioSciences, Inc.
43 antibodies
OriGene
3 antibodies
Aviva Systems Biology
2 antibodies
Acris Antibodies GmbH
1 antibody
Atlas Antibodies
1 antibody
NSJ Bioreagents
1 antibody
Invitrogen Antibodies
3 antibodies
Cusabio Biotech Co., Ltd
5 antibodies
ProSci
1 antibody
MyBioSource
5 antibodies
R&D Systems
2 antibodies
Abnova Corporation
1 antibody
Abbexa
6 antibodies
United States Biological
13 antibodies
Creative Diagnostics
3 antibodies
Leading Biology
1 antibody
MilliporeSigma / Merck KGaA
3 antibodies