LPL

gene product
LIPD
LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]
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AntibodyRefsTypeWBELICCIPIHCFC
Novus Biologicals
34 antibodies
R&D Systems
1 antibody
antibodies-online
164 antibodies
Biorbyt
24 antibodies
GeneTex
3 antibodies
OriGene
47 antibodies
Aviva Systems Biology
3 antibodies
NovoPro Bioscience Inc.
2 antibodies
NSJ Bioreagents
3 antibodies
Abgent
2 antibodies
LifeSpan BioSciences, Inc.
90 antibodies
Invitrogen Antibodies
6 antibodies
Abnova Corporation
7 antibodies
St John's Laboratory
2 antibodies
ProSci
1 antibody
Boster Biological Technology
3 antibodies
Affinity Biosciences
2 antibodies
MyBioSource
9 antibodies
Acris Antibodies GmbH
4 antibodies
Creative Biolabs
22 antibodies
Creative Diagnostics
7 antibodies
Atlas Antibodies
1 antibody
Proteintech Group
1 antibody
United States Biological
17 antibodies
RabMAbs
3 antibodies
GenWay
2 antibodies
Abbiotec
1 antibody
EMD Millipore
1 antibody
Sigma-Aldrich
1 antibody