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COG8
Component of oligomeric golgi complex 8DOR1, FLJ22315
This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]
Top validated antibodies |
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| Novus Biologicals |  NBP1-36949 |
1 references | Polyclonal |
WB
EL
IHC
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| Acris Antibodies GmbH | AP51007PU-N |
Polyclonal |
WB
EL
IHC
FC
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| Proteintech Group | 12661-1-AP |
1 references | Polyclonal |
WB
EL
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| Invitrogen Antibodies | PA5-29126 |
1 references | Polyclonal |
WB
ICC
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| antibodies-online | ABIN2034094 |
Polyclonal |
WB
ICC
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