STT3B

gene product
FLJ90106, SIMP, STT3-B
The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]
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38 antibodies from 13 providers.

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Antibody
Proteintech Group
1 antibody
Invitrogen Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
8 antibodies
Atlas Antibodies
2 antibodies
Novus Biologicals
2 antibodies
Abnova Corporation
2 antibodies
Biorbyt
6 antibodies
Affinity Biosciences
1 antibody
NovoPro Bioscience Inc.
1 antibody
antibodies-online
9 antibodies
St John's Laboratory
1 antibody
Creative Diagnostics
2 antibodies
MyBioSource
1 antibody